Arteries are formed by vein-derived endothelial

Full text

Turn on search term navigation

ARTICLE

Received 10 Apr 2014 | Accepted 4 Nov 2014 | Published 15 Dec 2014

Cong Xu1, Sana S. Hasan1, Inga Schmidt1, Susana F. Rocha1, Mara E. Pitulescu1, Jeroen Bussmann1,

Dana Meyen2, Erez Raz2, Ralf H. Adams1,3 & Arndt F. Siekmann1

Tissue vascularization entails the formation of a blood vessel plexus, which remodels into arteries and veins. Here we show, by using time-lapse imaging of zebrash n regeneration and genetic lineage tracing of endothelial cells in the mouse retina, that vein-derived endothelial tip cells contribute to emerging arteries. Our movies uncover that arterial-fated tip cells change migration direction and migrate backwards within the expanding vascular plexus. This behaviour critically depends on chemokine receptor cxcr4a function. We show that the relevant Cxcr4a ligand Cxcl12a selectively accumulates in newly forming bone tissue even when ubiquitously overexpressed, pointing towards a tissue-intrinsic mode of chemokine gradient formation. Furthermore, we nd that cxcr4a mutant cells can contribute to developing arteries when in association with wild-type cells, suggesting collective migration of endothelial cells. Together, our ndings reveal specic cell migratory behaviours in the developing blood vessel plexus and uncover a conserved mode of artery formation.

DOI: 10.1038/ncomms6758 OPEN

Arteries are formed by vein-derived endothelial tip cells

1 Max Planck Institute for Molecular Biomedicine, Roentgenstr. 20, 48149 Muenster, Germany. 2 Institute of Cell Biology, ZMBE, Von-Esmarch-Str. 56, 48149 Muenster, Germany. 3 University of Mnster, Faculty of Medicine, D-48149 Mnster, Germany. Correspondence and requests for materials should be addressed to A.F.S. (email: mailto:[email protected]

Web End [email protected] ).

NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications 1

ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758

The formation of new blood vessels is a crucial process during embryogenesis and growth14, but also in regenerative processes, such as wound healing and tissue

repair5. It entails the tight coordination of different cellular processes, such as proliferation, migration and lumen formation. In the early embryo, vascular development is often stereotypical, resulting in the formation of identical looking vascular networks6. By contrast, at later stages many vascular beds form via a plexus intermediate, which remodels into a hierarchical network of arteries and veins. Examples are the emerging skin blood vessels7 or the postnatally forming blood vessels of the mouse retina8. In addition, the vasculature in regenerating tissues, for instance in the regenerating zebrash n9 or during wound healing10, forms via a plexus.

In the current concepts of blood vessel formation, an initial pro-angiogenic cue species endothelial tip cells, which become motile and navigate through the avascular tissue11. Tip cells are followed by stalk cells. These maintain the connection to the preexisting vasculature, are less motile and subsequently establish a hierarchical network of arteries and veins to allow for efcient tissue perfusion12. Further studies have investigated the dynamics of endothelial cell migration during sprout outgrowth. Jakobsson et al.13 showed in an embryoid body sprouting assay that endothelial cells compete for the tip cell position. Another study using a mouse aortic ring assay suggested that this competition and the ensuing cell-mixing are important for the proper outgrowth of angiogenic sprouts14.

Despite the insights these studies provided, they were performed in in vitro settings, which lack proper arterial-venous differentiation of the forming vascular plexus and tissue perfusion. So far, in vivo imaging of the forming vasculature has been mainly performed in transparent zebrash embryos1517. However, these studies have not included vascular beds that form via a plexus intermediate. Therefore, despite the signicance of vascular plexus formation and subsequent remodelling for tissue perfusion, we still have a poor understanding of endothelial cell dynamics during these processes. In particular, we do not understand how endothelial cells coordinate the sprouting of new vessels with the establishment of larger arteries and veins.

In this study, we take advantage of the optical clarity of the adult zebrash n to perform in vivo time-lapse imaging of the complex cell migratory behaviours during blood vessel formation in regenerating tissues. Our results show that endothelial tip cells not only invade avascular tissues, but that they can subsequently change their direction of migration and ultimately migrate against the advancing vascular front. Furthermore, we show that this behaviour is necessary for the proper formation of arteries. In addition, we observe proliferating endothelial cells in tip and stalk cells of venous origin, while arterial endothelial cells proliferate less. Through genetic lineage tracing in the mouse retina, we provide evidence that this mode of artery formation is conserved in other vascular beds that form via a plexus intermediate. We implicate the chemokine receptor Cxcr4a in regulating these migratory behaviours and suggest that a tissue-intrinsic mode is responsible for the generation of a Cxcl12a chemokine gradient. We nally demonstrate through cell transplantation experiments that endothelial cells show a collective cell migration behaviour.

ResultsBlood vessels regenerate via an intermediate vascular plexus. To visualize regenerating blood vessels, we analysed vascular dynamics during n regeneration in adult transgenic zebrash. In Tg(i1a:EGFP)y1 zebrash, all endothelial cells are labelled by EGFP expression18, while, in Tg( 0.8t1:RFP)hu5333 sh, arterial

endothelial cells are labelled by high RFP expression19. Confocal

imaging of ns of double transgenic animals revealed that, in the distal part, each n ray contained a medially located artery, which was anked by two veins (Fig. 1ad). These vessels furthermore showed distinct topologies in respect to the bones of the n rays. While the artery ran within the bone, the veins were located outside of the bony rays (Supplementary Fig. 1ag). Thus, the vasculature of the zebrash n consists of a regular pattern of arteries and veins, which can be visualized using different transgenic zebrash lines.

We next amputated the ns of double transgenic animals and observed blood vessel growth within the regenerating tissue (Fig. 1e). In agreement with previous observations9, we detected the formation of a dense vascular plexus at 3 days post amputation (Fig. 1f, 3 d.p.a.). This plexus, after bifurcating, subsequently remodelled into a single medial artery and two lateral veins (Fig. 1f, 514 d.p.a., see also Supplementary Fig. 2). We could distinguish different areas within the vasculature distally to the established artery and vein during this outgrowth phase. Most distally, we observed a sprouting front invading the avascular tissue, followed by a remodelling vascular plexus (Fig. 1f). Within this plexus, we could distinguish arterial fated endothelial cells by virtue of RFP expression (see also Supplementary Fig. 2c). Therefore, our double transgenic zebrash allowed for the detailed observation of the forming vasculature via a plexus intermediate during tissue regeneration.

Time-lapse imaging reveals vein cells contribute to arteries. To detect endothelial cell movements, and arterial differentiation, we combined Tg(i1a:nEGFP)y7, labelling endothelial cell nuclei20 with Tg( 0.8t1:RFP)hu5333 sh and performed time-lapse

imaging for 24 h, starting at 9 d.p.a. (Supplementary Movie 1). Representative images taken every 6 h can be seen in Fig. 2. At this stage, the n ray started to bifurcate and consisted of two arteries anked by a shared vein in the middle and two lateral veins. We then colour coded endothelial cells located in arterial and venous positions and followed their migratory paths (Fig. 2b,c). This analysis revealed prominent differences in migratory behaviours between venous- and arterial-derived endothelial cells during tissue vascularization. Cells located in venous positions migrated more extensively towards the sprouting front than arterial-derived endothelial cells (compare blue/white dots and tracks with pink ones in Fig. 2b,c). Furthermore, some of these vein-derived endothelial tip cells subsequently changed their orientation, turned medially and nally migrated against the direction of the moving vascular front (arrows in Fig. 2c, time stamp in d, schematic drawings in e, f). Strikingly, we observed that the cells that had turned medially formed the remodelling artery in the centre of each n ray (Fig. 2b, 23:45 h time point, inset). By contrast, we did not observe endothelial cells coming from the artery in venous blood vessels. We furthermore quantied proliferation of vein- and artery-derived endothelial cells (Supplementary Fig. 3a,b; Supplementary Movie 2). Whereas about 50% of venous endothelial cells divided within 24 h, less than 20% of artery-derived endothelial cells proliferated (Supplementary Fig. 3e). We detected both dividing tip- and stalk cells (Supplementary Fig. 4 and Supplementary Movie 3). Thus, our time-lapse analysis of blood vessel growth reveals a venous origin of arterial endothelial cells and shows that distinct migratory properties of endothelial tip cells contribute to proper blood vessel morphogenesis during tissue regeneration. It also shows that pronounced differences exist in endothelial cell proliferation between arteries and veins.

Tip cells in the mouse retinal plexus contribute to arteries. We next wanted to know whether blood vessel formation in other

2 NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications

NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758 ARTICLE

Vein

Artery

Vein

ArteryOverlay

V V

Tg(fli1a:EGFP)y1 Tg(0.8flt1:RFP)hu5333

Sprouting

front

Established

artery/vein

Remodelling

plexus

Bifurcation

Ray1 Ray2

Lobes Cleft

Distal Proximal

Bony ray

Tg(0.8flt1:RFP) hu5333

Tg(fli1a:EGFP) y1

Area imaged

Distal Proximal

Regenerated Fin

Dorsal Ventral

0 d.p.a. 3 d.p.a. 7 d.p.a. 14 d.p.a.

5 d.p.a.

Figure 1 | Visualizing blood vessels in the regenerating zebrash n. (a,a0) Tg(i1a:EGFP)y1 labels all n blood vessels. (b,b0) Tg( 0.8t1:RFP)hu5333

preferentially labels arterial endothelial cells. (c,d) Schematic drawings of the zebrash n vasculature, indicating the ray bifurcation, arteries (A) and veins(V). (e) Schematic of zebrash n, indicating plane of amputation and imaged area. (f) Overlay of Tg(i1a:EGFP)y1 and Tg( 0.8t1:RFP)hu5333 at different

stages of n regeneration highlighting the medially located arterial cells in yellow. Inset (f0) shows remodelling vascular plexus, which is located proximal to the sprouting front and distally to the established arteries and veins. Scale bar in a is 80 mm, in a0 is 20 mm and 200 mm in f. Representative images from a total of three zebrash imaged per stage.

vascular beds that are established via a plexus intermediate occurs by a similar mechanism. We chose to investigate the mouse retinal vasculature due to the availability of genetic tools that allow for lineage tracing of different cell populations. To genetically label endothelial tip cells located at the vascular front, we generated double transgenic mice containing a R26-tomato-EGFP reporter21 in conjunction with a tamoxifen-inducible iCre-ERT2 cassette under the control of the endothelial-specic molecule-1 (Esm-1) promoter22 (Fig. 3a). Previous studies showed Esm-1 mRNA expression mainly in endothelial tip cells23,24. Accordingly, we observed specic expression of EGFP in endothelial cells at the vascular front 12 h after tamoxifen injection (Fig. 3bd, bracket). To track labelled cells over time, we analysed the location of EGFP expressing

cells within the vasculature after 24 or 48 h of tamoxifen injection (Fig. 3eg, 48 h time point shown). We observed a striking bias of EGFP-positive cells towards the developing arteries, while we did not nd a signicant contribution of EGFP-positive cells to developing veins (Fig. 3g, arteries are marked by arrows, veins by arrowheads). After 48 h, about 15% of the arterial vessel area was occupied by EGFP-positive cells, while only about 1.5% of the venous vessel area was occupied by EGFP-positive cells (Fig. 3h). This suggests that similar to the vasculature in the regenerating zebrash n, endothelial tip cells in the mouse retina can contribute to nascent arteries, while they only marginally contribute to forming veins. EdU incorporation experiments in recombined endothelial cells and their descendants indicated proliferation of these cells

NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications 3

ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758

24-h live imaging of 9-d.p.a. regenerating wild-type fin vessels

Tg(fli1a:nEGFP)y7; Tg(0.8flt1:RFP)hu5333

00:00:00.000 06:00.00.000 12:00.00.000 18:00.00.000 23:45:00.000

Bifurcated fin rays

cell trackingNo tracking

Vessel front

Vein

Artery

Shared vein

Lateral vein derived Artery derived Medial vein derived

Artery

Dot tracking

Regenerated

vessels

Vessel regeneration

Artery Shared veinRegenerated artery

Vein Vein Vein

Artery

Vein

0 h 24 h

Dot and line

Time stamp

Figure 2 | Time-lapse imaging of regenerating blood vessels reveals contribution of vein-derived tip cells to the forming artery. (a) Still images taken every 6 h from a 24-h time-lapse movie on 9 d.p.a. n regenerate of wild-type sh. (b) Tracking of individual cells deriving form the lateral vein (white dots), the artery (pink dots) or the medial vein (blue dots). While arterial cells hardly contribute to the advancing front, vein-derived cells contribute to the newly forming artery (inset at 23:45 h time point). (c) Tracks of labelled cells in (b). White arrows indicate migration paths of lateral vein-derived endothelial cells, while blue arrows indicate migration paths of medial vein-derived endothelial cells. Note change in migration direction. (d) Time stamp of tracked endothelial cells. (e) Schematic drawing of vessel front in the regenerated n of wild-type sh at 10 d.p.a. Arteries and veins are indicated.(f) Schematic drawing of wild-type n vasculature regenerated within 24 h from 9 d.p.a. Scale bar, 100 mm; d.p.a. days post amputation. Representative

movie of a total of three movies is shown.

(Supplementary Fig. 5), accounting for an increase in labelled endothelial cells at later time points.

Expression of cxcr4a and its ligands cxcl12a and cxcl12b. We reasoned that pro-migratory genes specically expressed by endothelial tip cells might control the observed distinct migratory behaviours of arterial-fated endothelial cells. We and others had previously shown that the chemokine receptor Cxcr4 was specically expressed in endothelial tip cells, both in mouse23,24 and zebrash (cxcr4a)15. We therefore analysed expression of cxcr4a during n regeneration. To achieve cellular resolution, we generated transgenic animals expressing uorescent proteins under the control of the cxcr4a, cxcl12a and cxcl12b promoters25, respectively (see Methods). To visualize the vasculature in addition to transgene expression, we crossed these sh into the Tg( 0.8t1:RFP)hu5333 background. In Tg(cxcr4a:YFP)mu104

zebrash, we observed YFP expression mainly in the centre of regenerating n rays, where it overlapped with individual endothelial cells in a salt and pepper distribution (Fig. 4aa00, compare cells marked by arrows and arrowheads). Tg(cxcl12a:CFP)mu146 sh showed expression of CFP in nonendothelial cells located in the centre of regenerating n rays, in the area of the forming artery (Fig. 4bb00). Finally, in

Tg(cxcl12b:YFP)mu105 sh, we observed YFP expression in lamentous structures, most probably nerve bres (Fig. 4cc00)26.

These staining patterns were mirrored by in situ hybridization results (Supplementary Fig. 6). Thus, mRNAs for the chemokine receptor Cxcr4a and for the ligands Cxcl12a and Cxcl12b are expressed in the regenerating zebrash n.

Defects of cxcr4a and cxcl12a mutants in arterial patterning. To address the relevance of cxcr4a in endothelial cell migration, we analysed the regenerating vasculature in homozygous cxcr4aum20 mutant zebrash27. Although the total endothelial cell numbers were not different between wild type and cxcr4aum20 mutant sh at any of the analysed time points, we detected a strong reduction in endothelial cell numbers, vascular coverage and vessel length in the centre of the n rays in cxcr4aum20 mutants (Supplementary Fig. 7), suggesting that artery formation was severely impaired (Fig. 4df, 14 d.p.a. time point shown, Supplementary Tables 1 and 2). We also observed ectopically located Tg( 0.8t1:RFP)hu5333-positive arterial cells in mutant

sh, often running in parallel with veins (Fig. 4e, white arrowheads). We observed similar defects in arterial patterning in cxcl12at30516 mutant zebrash28 (Fig. 4gi, 14 d.p.a. time point shown, Supplementary Fig. 8, Supplementary Tables 1 and 2). By contrast, cxcl12bmu100 mutant zebrash15 did not show differences in arterial patterning when compared with wild-type siblings (Supplementary Fig. 9, Supplementary Tables 1 and 2). Despite these patterning defects, differentiation of arterial cells appeared unaffected, as we observed Tg( 0.8t1:RFP)hu5333-

positive endothelial cells in cxcr4aum20 mutants, albeit in ectopic locations. Thus, Cxcr4a-Cxcl12a signalling appears to be necessary for proper arterial morphogenesis, but not differentiation. Quantifying endothelial cell proliferation in cxcr4aum20 mutants (Supplementary Fig. 3c,d and Supplementary Movie 4), we detected a reduction in endothelial cell proliferation in both veins and arteries in these mutants by about 50% (Supplementary Fig. 3e). Therefore, while the endothelial cell migratory defects observed in cxcr4aum20

4 NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications

NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758 ARTICLE

Ubiquitous promoter

Esm1 promoter

Ubiquitous promoter

% of vessel area occupied

by EGFP-positive cells

Artery

RFP

EGFP

Vein

iCre-ERT2

+Tamoxifen at P4

EGFP

12 h 24 h 48 h

V A

IsolectinB4

EGFP

12 h after tamox.

Overlay

V A

EGFP Overlay

48 h after tamox.

100 m

Figure 3 | Genetic lineage tracing of tip cells in the mouse retinal vascular plexus. (a) Schematic of genetic lineage tracing and transgenic lines used. (b) Isolectin B4 staining of the retinal vasculature at P6. Bracket indicates vascular front. (c) Location of EGFP expressing cells at the vascular front 12 h after tamoxifen administration. (d) Overlay of isolectin B4 and EGFP channels. Remodelling arteries (A) and veins (V) are marked. (e) Isolectin B4 staining of the retinal vasculature at P6. (f) Location of EGFP expressing cells at the vascular front 48 h after tamoxifen administration. (g) Overlay of isolectin B4 and EGFP channels. Remodelling arteries (A) and veins (V) are marked. Arrows indicate EGFP-positive endothelial cells in arteries, while arrowheads indicate EGFP-negative veins. (h) Percentage of EGFP-expressing endothelial cells in arteries and veins at different time points after tamoxifen administration. Scale bar, 100 mm. For each time point ve mice were analysed. *Po0.05; t-test, error bars indicate s.e.m.

mutants specically affected forming arteries, the proliferative defects were apparent both in arteries and veins.

cxcr4aum20 mutant endothelial cells show defective migration. To understand how Cxcr4a signalling inuences artery formation, we performed time-lapse imaging of cxcr4aum20 mutant sh for 24 h, starting at 9 d.p.a. These studies revealed that in the absence of Cxcr4a signalling, endothelial tip cells failed to turn medially, and instead continued to migrate as a vascular front (Fig. 5ac, time stamp in d, schematic drawings in e,f, Supplementary Movie 5, and compare with Fig. 2af). Consequently, no artery formed in the centre of the regenerating n ray. By contrast, we observed Tg( 0.8t1:RFP)hu5333-positive endothelial cells adjacent to the

laterally located veins. Thus, Cxcr4a signalling is indispensible during the coordination of the complex endothelial cell movements that are necessary for artery formation during tissue regeneration.

Cell transplantations reveal collective cell migration. Migrating cells can either follow guidance cues individually or migrate as groups of cells29. Cxcr4 signalling in zebrash has been described to play a role in single-cell migration regulating germ cell

migration to the gonad and in collective cell migration during the formation of the lateral line30. To address whether Cxcr4a signalling within endothelial cells was necessary for single cell or collective cell migration, we generated chimeric embryos consisting of cxcr4aum20 mutant and wild-type cells and let them grow to adulthood. To visualize donor-derived endothelial cells, we transplanted double Tg(i1a:EGFP)y1; Tg( 0.8t1:

RFP)hu5333 cells into single Tg( 0.8t1:RFP)hu5333 hosts. We

subsequently analysed sh that had donor- and host-derived blood vessels in their ns after amputation (Fig. 6a).

Of a total of about 5,200 transplanted embryos, 14 showed donor-derived cells in different adult ns (Supplementary Table 3). We observed two distinct patterns of donor cell contribution: either the vasculature of an entire given n ray was donor-derived (Fig. 6bd00, arrows mark artery) or only a fraction of venous and/or arterial cells was donor-derived (Fig. 6ej00). In situations, where the entire n ray vasculature was donor-derived, transplanted endothelial cells behaved according to the donor genotype. Wild-type cells transplanted to either wild-type hosts (Fig. 6bb00) or to cxcr4aum20 mutants (Fig. 6cc00) formed normal arteries, while cxcr4aum20 mutant endothelial cells transplanted into wild-type hosts did not form arteries in the proper location (Fig. 6dd00). These observations suggest that

NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications 5

ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758

Transgenic reporter fish, 2 d.p.a.

Tg(cxcr4a:YFP)mu104 Tg(0.8flt1:RFP)hu5333 Overlay

14-d.p.a. regenerated vessels

Tg(fli1a:nEGFP)y7; Tg(0.8flt1:RFP)hu5333

cxcr4a

cxcl12a

EC number (total) EC number (centre)

Vessel length (centre)

300 NS

250

****

200

centre

150

100

Sib

Mut

0 Sib

Mut

Vessel coverage (centre)

10,000

1,000

8,000

800

****

6,000

600

4,000

400

Tg(cxcl12a:CFP)mu146

Tg(0.8flt1:RFP)hu5333 Overlay

2,000

200

0 Sib

Mut

0 Sib

Mut

Sibling

cxcr4aum20

300

EC number (total) EC number (centre)

Vessel coverage (centre) Vessel length (centre)

250

200

****

150

100

Tg(cxcl12b:YFP)mu105

0 Sib

Mut

0 Sib

Mut

10,000 ****

1,000

****

8,000

800

6,000

600

4,000

400

2,000

200

cxcl12at30516

0 Sib

Mut

0 Sib

Mut

Figure 4 | The chemokine receptor cxcr4a and its ligand cxcl12a are required for proper arterial patterning during n regeneration. Dashed lines indicate amputation planes in ac00. (a) Tg(cxcr4a:YFP)mu104 sh reveal YFP expression in individual cells in the centre of the regenerating n ray.

(a0) Tg( 0.8t1:RFP)hu5333 labelled blood vessels. (a00) Overlay of red and yellow channels reveals expression of YFP in individual endothelial cells (arrows),

while neighbouring endothelial cells do not express YFP (arrowheads). (b) CFP expression in the centre of the regenerating n in Tg(cxcl12a:CFP)mu146

transgenic zebrash. (b0) Tg( 0.8t1:RFP)hu5333 labelled blood vessels. (b00) Overlay of red and blue channels. (c) YFP expression in lamentous structures

(arrowheads) extending into the regenerating n in Tg(cxcl12b:YFP)mu105 transgenic zebrash. (c0) Tg( 0.8t1:RFP)hu5333 labelled blood vessels.

(c00) Overlay of red and yellow channels. (d) Fin vasculature in wild-type sibling 14 d.p.a. Arrows indicate Tg( 0.8t1:RFP)hu5333-positive endothelial cells in

the centre of the n ray. (e) cxcr4aum20 mutant; arrowheads indicate ectopic Tg( 0.8t1:RFP)hu5333-positive endothelial cells. (f) Quantication of artery

formation defects in cxcr4aum20 mutants. Endothelial cell numbers, vessel coverage and length are reduced in the centre. (g) Fin vasculature in wild-type sibling 14 d.p.a. Arrows indicate Tg( 0.8t1:RFP)hu5333-positive endothelial cells in the centre of the n ray. (h) cxcl12at30516 mutant; arrowheads

indicate ectopic Tg( 0.8t1:RFP)hu5333-positive endothelial cells. Scale bar (ac,e,h), 100mm. (i) Quantication of artery formation defects in cxcl12at30516

mutants. Endothelial cell numbers, vessel coverage and length are reduced in the centre. NS, not signicant, **Po0.01, ****Po0.0001; MannWhitney U-test. Twenty individual n rays from ve sh were analysed.

cxcr4a functions endothelial cell autonomously during artery formation in regenerating ns.

In mosaic cases (Fig. 6ej00), we observed that donor (Fig. 6e,g,i,ff00,hh00,jj00, white arrowheads) and host cells (Fig. 6e0,g0,i0,ff00,hh00,jj00, blue arrowheads) could contribute to arteries, irrespective of their genotypes. These ndings suggest that endothelial cells of the forming artery engage in collective migration, which allows for wild-type cells to rescue the migratory phenotype of cxcr4aum20 mutant cells. They furthermore suggest that, while showing migration defects, cxcr4aum20-decient endothelial cells can properly differentiate into the arterial lineage.

Ubiquitous overexpression of Cxcl12a rescues cxcl12a mutants. Our analysis of cxcl12a expression during n regeneration (Fig. 4bb00) suggested that Cxcl12a might be distributed in a graded manner with higher concentrations in the centre of the n. To determine whether graded Cxcl12a distribution was indeed necessary for proper artery formation, we ubiquitously overexpressed Cxcl12a-mCherry for 14 days during n regeneration using Tg(Cry.kop.HSP:mutSDF1a.mCherry. globin30UTR)mu4 sh. Overexpression of Cxcl12a-mCherry did not affect n regeneration in wild-type siblings (Fig. 7, compare values for sibling in Fig. 7a with heat-shock sibling sh in Fig. 7b). Importantly, the arterial defects in cxcl12at30516 mutant zebrash were completely rescued by ubiquitous overexpression

of Cxcl12a-mCherry (Fig. 7b, Supplementary Table 4). Surprisingly, we detected strong accumulation of the fusion protein in newly forming bone segments in the regenerates of both siblings and mutants (Fig. 7b, white arrowheads). We did not detect Cxcl12a-mCherry in the uninjured bone proximal to the amputation plane (Fig. 7b, proximal to the dotted line). The remainder of the regenerated n, especially the most distal tissues, displayed faint Cxcl12a-mCherry signal, which accumulated in a dot-like pattern. Thus, although ubiquitously expressed under the control of a heat-shock promoter, Cxcl12a-mCherry accumulated in a tissue-restricted manner in regenerating n tissue, with higher concentration detected within newly forming bones.

DiscussionIn this study, we have analysed endothelial cell migration during blood vessel plexus formation and remodelling in an in vivo setting: the regenerating zebrash n. Our results show that endothelial cells within growing blood vessel sprouts initially invade the avascular area. The signalling process that is most likely responsible for this behaviour is the VEGF pathway. During n regeneration, vegf-a mRNA is being expressed in the n regenerate and inhibition of VEGF signalling abolishes n vessel outgrowth31. In addition, a VEGF gradient was postulated to drive retinal angiogenesis32. Studies in the mouse retina and in cell culture have shown that the exposure to VEGF can lead to the induction of tip cell specic genes, such as the Notch ligand Dll4 and the

6 NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications

NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758 ARTICLE

24-h live imaging of 9-d.p.a. regenerating cxcr4a mutant fin vessels

Tg(fli1a:nEGFP)y7; Tg(0.8flt1:RFP)hu5333

00:00:00.000 06:00.00.000 12:00.00.000 18:00.00.000 23:45:00.000

Bifurcated fin rays

Vein

Vessel front

cell trackingNo tracking

Artery

Shared vein

Lateral vein derived Artery derived Medial vein derived

Dot tracking

Dot and line

Regenerated

vessels

Vessel regeneration

Artery Shared veinRegenerated artery

Vein Vein Vein

Artery

Vein

0 h 24 h

Time stamp

Figure 5 | Time-lapse imaging of regenerating blood vessels in cxcr4aum20 mutant sh. (a) Still images taken every 6 h from a 24 h time-lapse movie on 9 d.p.a. n regenerate of cxcr4aum20 sh. (b) Tracking of individual cells deriving form the lateral vein (white dots), the artery (pink dots) or themedial vein (blue dots). (c) Tracks of labelled cells in (b). White arrows indicate migration paths of lateral vein-derived endothelial cells, while blue arrows indicate migration paths of medial vein-derived endothelial cells. Note persistent migration of tracked endothelial cells in the direction of the growing regenerate. (d) Time stamp of tracked endothelial cells. (e) Schematic drawing of vessel front in the regenerated n of cxcr4aum20 sh at 10 d.p.a. Arteries

and veins are indicated. (f) Schematic drawing of cxcr4aum20 n vasculature regenerated within 24 h from 9 d.p.a. Scale bar, 100 mm; d.p.a., days post amputation. Representative movie of a total of three movies.

chemokine receptor Cxcr4 (refs 11,23,24,33). Although activation of Notch signalling via Dll4 in neighbouring cells leads to the suppression of the tip cell phenotype34, Cxcr4a induction would change the tip cells responsiveness to guidance cues present in the environment. As we show that the chemokine ligand Cxcl12a is likely enriched in the central area of the n ray, Cxcr4a expressing endothelial cells would respond to this chemokine and change their direction of migration towards the centre of the ray, allowing for proper arterial morphogenesis. Accordingly, our cxcr4aum20 mutant analysis revealed that in this setting, endothelial cells failed to turn medially, but continued to migrate in the direction of the avascular area. Therefore, Cxcr4a-mediated medial migration of tip cells would be necessary to balance the directionality imposed on the outgrowing vasculature by VEGF.

A dependence on Cxcr4 signalling for artery formation was recently observed in the mouse skin vasculature. In this setting, nerves secrete Cxcl12, while a subset of endothelial cells in the surrounding vascular plexus expresses Cxcr4 (ref. 35). In the absence of Cxcr4 signalling vessel nerve alignment is disrupted. This suggests that in the developing mouse skin vasculature, endothelial cell migration might occur similarly to what we observe in the regenerating zebrash n. In addition, Strasser et al.24 observed that, in retinae treated with the Cxcr4 inhibitor AMD3100, long sprouts formed that failed to connect laterally to neighbouring sprouts, a phenotype that corresponds to our observations during the live imaging of cxcr4aum20 mutants. This, together with our genetic lineage tracing of tip cells in the retina, suggests that the morphogenetic movements we observed during vascular plexus formation in the regenerating n might be a general principle.

Despite the important role of Cxcr4a signalling during arterial morphogenesis, differentiation of arterial cells appears to be

unaffected in cxcr4aum20 mutant zebrash. We readily observe Tg( 0.8t1:RFP)hu5333-positive blood vessels in cxcr4aum20 mutant

ns, albeit in random locations. Proper arterial differentiation of endothelial cells lacking Cxcr4a function is furthermore supported by our cell transplantation experiments, where cxcr4aum20 mutant cells could contribute to arteries when surrounded by wild-type cells. This is in line with observations on Cxcr4-expressing endothelial cells from the skin of mouse embryos. In this setting, Cxcl12 exposure did not lead to arterial differentiation, while VEGF-A exposure could induce the expression of the arterial marker gene ephrinB2 also in Cxcr4 mutant endothelial cells35. One important difference between the mouse skin and the regenerating n vasculature is that, in the n, arterial differentiation does not seem to depend on the proper location of the arterial-fated endothelial cells. In the mouse skin, only endothelial cells that are in close proximity to VEGF providing nerves can differentiate into arteries7,36. One reason for this difference might be that, during regeneration, tissue VEGF levels are high enough to allow for arterial differentiation throughout the entire n.

Our data furthermore show that endothelial cell proliferation during vascular plexus formation differs between arterial and venous endothelial cells. We detect higher proliferation in venous endothelial cells. These ndings are in agreement with previous studies in the mouse retina, which found persistent endothelial cell proliferation in veins, but not in arteries during vascular maturation37. Therefore, veins appear to constitute the main source of endothelial cells for newly forming blood vessels. In the mouse retina we nd that descendants of previously labelled endothelial tip cells can proliferate during blood vessel formation and thereby account for an increase in the number of labelled endothelial cells. Our zebrash data also show that both tip and

NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications 7

ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758

Transplant Grow to adulthood Analyse fin vasculature

Regenerated fin

Vasculature of wholeray donor derived Mosaic ray vasculature

Donor cells

Donor

+host

Overlay Donor cells

Donor

+host

Overlay Donor cells

Donor

+host

Overlay

Donor: Tg(fli1a:EGFP)y1 ;Tg(0.8flt1:RFP)hu533 Host: Tg(0.8flt1:RFP)hu533

WT --> WT WT --> cxcr4a

um20

cxcr4aum20 --> WT

Figure 6 | Analysis of cxcr4a function in chimeric n vasculature. (a) Schematic drawing of transplantation procedure. Cells from double transgenic Tg(i1a:EGFP)y1; Tg( 0.8t1:RFP)hu5333 donors were transplanted into single Tg( 0.8t1:RFP)hu5333 hosts. Two different scenarios were observed: Either the

vasculature of the whole ray was donor-derived (bd00), or a mosaic ray vasculature, consisting of donor and host-derived endothelial cells formed (ej00). (bb00) In wild type to wild-type transplants, normal n blood vessels formed. Arrow in b00 marks artery (n 8 adult zebrash). (cc00) When wild-type cells

were transplanted into cxcr4aum20 mutant hosts, normal arteries could form (arrow in c00, n 2 adult zebrash). (dd00) When cxcr4aum20 mutant cells were

transplanted into wild-type hosts and formed the vasculature of an entire n ray, arteries showed similar patterning defects as in cxcr4aum20 mutants (arrow in d00, n 3 adult zebrash). (ef00) In a control mosaic situation, both donor (white arrowhead, ff00) and host-derived (blue arrowhead, ff00) wild-type

cells contributed to forming arteries. Dashed box in (e) indicates magnied area in ff00 (n 8 adult zebrash). (gh00) In a mosaic situation, both donor-

derived wild-type cells (white arrowheads in hh00) and host-derived cxcr4aum20 mutant cells (hh00, blue arrowheads) contributed to forming arteries. Dashed box in (g) indicates magnied area in hh00 (n 2 adult zebrash). (ij00) In a mosaic situation, both donor-derived cxcr4aum20 mutant cells

(white arrowheads in jj) and host-derived wild-type cells (jj00, blue arrowheads) contributed to forming arteries. Dashed box in i indicates magnied area in jj00 (n 3 adult zebrash). Scale bars are 50 mm in i00 and 20 mm in j00.

stalk cells can proliferate during vascular outgrowth. This is in agreement with previous studies in developing zebrash inter-segmental vessels3840. We observe a reduction in endothelial cell proliferation both in arteries and veins in cxcr4aum20 mutants. This is in contrast to the observed cell migration defects in cxcr4aum20 mutants, which specically affect newly forming arteries. At present it is not clear whether the observed cell proliferation defects are due to a direct effect of cxcr4a signalling

in both endothelial cell populations or due to perfusion defects, which might result from arterial malformations.

Chemokines play important roles in guiding the migration of various cell types, such as leukocytes41, endothelial cells42, endodermal cells43, germ cells30 and neurons44. They mainly function through the formation of a gradient, which provides positional information or through the activation of integrin signalling30. The zebrash genome contains two cxcl12

8 NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications

NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758 ARTICLE

homologues30. In the embryo, cxcl12bmu100 mutants recapitulate the vascular phenotypes observed in cxcr4aum20 mutants15,27. Surprisingly, blood vessel formation during n regeneration was unaffected in cxcl12bmu100 mutants, while cxcl12at30516 mutants showed phenotypes similar to those of cxcr4aum20 mutants. It will be interesting in the future to determine the reason for this apparent switch in Cxcr4a ligand usage between embryonic stages and during regeneration.

The formation of chemokine gradients has been under intense investigation in recent years. One breakthrough study described the generation of chemokine gradients via ligand sequestration in

the surrounding tissue by a decoy chemokine receptor, Cxcr7 (ref. 45). More recent reports show that migrating tissues can self-generate chemokine gradients46,47. We nd selective accumulation of ubiquitously overexpressed Cxcl12a-mCherry protein in newly forming bones during zebrash n regeneration, which can fully rescue artery formation in cxcl12at30516 mutants. This nding suggests that, while the precise mechanism is currently unknown, the regenerating n tissue is either able to selectively degrade Cxcl12a protein outside of the bone or to stabilize it within the bone. Further studies will help to distinguish between these two options.

Our cell transplantation experiments showed that cxcr4aum20 mutant cells could contribute to the forming artery when surrounded by wild-type cells. This demonstrates that endothelial cells can also cooperate during plexus remodelling and that collective cell migration occurs during this process. Similar cell behaviours play a role during Cxcr4b controlled lateral line migration in zebrash embryos48. In this setting, cxcr4bt26035 mutant cells can migrate normally in a wild-type primordium49. This indicates that, also in the vasculature, the organization of collective cell migration might be dependent on competition and cooperation between endothelial cells29.

Vascular malformations and patterning defects, including stenosis and arteriovenous shunts, can lead to life-threatening conditions in humans, underscoring the importance of understanding the mechanisms that lead to proper blood vessel sprouting and artery formation. Previous studies have used in vitro blood vessel sprouting assays to study endothelial cell dynamics during blood vessel growth. Arima et al.14 used an aortic ring sprouting assay and elegant cell tracking methods to show that endothelial cells in elongating branches are highly dynamic. The authors observed cell mixing and overtaking at the tip position. Interestingly, they also noticed individual endothelial cells that migrated opposite to the direction of the elongating sprout. The authors attributed this behaviour to loss of VEGF gradient formation in their culture setting. Our results now argue that this change in migratory direction could rather reect the initiation of artery formation, not readily assessable in the aortic ring assay. In an embryoid body sprouting assay, Jakobsson et al.13 also observed endothelial cell mixing and shufing of tip cells. These behaviours suggested competition between endothelial cells for the tip cell position, which was dependent on the relative levels of VEGF receptors and the Notch ligand Dll4. However, also in this assay, normal artery differentiation does not take place, precluding the analysis of the complete sprouting and remodelling programme. We now show that during zebrash n regeneration and in the developing mouse retinal vasculature, endothelial tip cells are derived from veins and that these tip cells can contribute

14 d.p.a. fin regenerated vessel

cxcl12at30516 wild-type sibling and mutant

Tg(fli:nEGFP)y7;

Tg(0.8flt1:RFP)hu5333

Sib Mut

Sib

Mut

EC number (total) EC number (centre)

Vessel length (centre)

300 250 200 150 100

****

0 Sib Mut

Vessel coverage (centre)

0 Sib Mut

10,000

****

1,000

****

8,000

800

600

6,000

4,000

400

2,000

200

0 Sib Mut

Tg(fli:nEGFP)y7; Tg(0.8flt1:RFP)hu5333 Tg(Cry.kop.HSP:mutSDF1a.mCherry.globin3UTR)mu4

Sib Mut

Sib

Mut

Figure 7 | Global overexpression of Cxcl12a-mCherry rescues the vascular phenotype of cxcl12t30516 mutant sh. White dashed boxes

indicate central areas quantied. Fin vasculature was analysed at 14 d.p.a. Dashed lines indicate amputation planes. (a) Heat-shocked control wild type and cxcl12at30516 mutant sh not carrying the Tg(Cry.kop.HSP:mutSDF1a.

mCherry.globin30UTR)mu4 transgene. White arrowheads indicate ectopic Tg( 0.8t1:RFP)hu5333-positive endothelial cells in cxcl12at30516 mutants.

Endothelial cell numbers, vessel coverage and vessel length are reduced in cxcl12at30516 mutant sh. (b) Heat-shocked wild type and cxcl12at30516

mutants carrying the Tg(Cry.kop.HSP:mutSDF1a.mCherry.globin30UTR)mu4 transgene. None of the assayed parameters differs between heat-shocked wild type and cxcl12at30516 mutants. Note accumulation of ubiquitously overexpressed Cxcl12a-mCherry protein in bony rays (white arrowheads) but not in the joints (blue arrowheads) between bone segments. ****Po0.0001;

MannWhitney U-test, NS, not signicant; n 8 adult zebrash per stage.

Scale bar, 100 um.

EC number (total)

EC number (centre)

300 250 200 150 100

0 hs sib hs mut

Vessel coverage (centre) Vessel length (centre)

10,000

1,000

8,000

800

6,000

600

4,000

400

2,000

200

0 hs sib hs mut

NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications 9

ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758

to forming arteries. Thus, our results provide a new framework for an understanding of the coordinate migratory behaviours of endothelial cells that allow for the proper sprouting and subsequent remodelling of arteries and veins in a vascular plexus.

Methods

Zebrash Strains and Fin amputations. Previously described zebrash lines were Tg(i1a:EGFP)y1 (ref. 18), (Tg(i1a:nEGFP)y7 (ref. 20), Tg( 0.8t1:RFP)hu5333

(ref. 19), Tg(cxcl12bBAC:YFP)mu105 (ref. 25), cxcr4aum20 (ref. 27), cxcl12bmu100 (ref. 15), cxcl12at30516 (ref. 28). Zebrash of 518 months of age were used. Fin amputations were performed as previously described50. All animal experiments were performed in compliance with the relevant laws and institutional guidelines and were approved by local animal ethics committees of the Landesamt fr Natur, Umwelt und Verbraucherschutz Nordrhein-Westfalen.

Generation of transgenic lines. We used Bacterial articial chromosome (BAC) recombineering as described previously to generate transgenic lines25. To generate Tg(cxcr4aBAC:YFP)mu104 and Tg(cxcl12aBAC:CFP)mu146 animals, the start codonof the cxcr4a and cxcl12a gene in the BAC clone CH73-268G8 and CH73-353M13 was replaced with a Citrine or Cerulean cassette using Red/ET recombineering (GeneBridges). The Citrine cassette was amplied by PCR from pCS2 Citrine_kanR

with the primers cxcr4a _HA1_GFP_fw (50-ttattttttatttttacggctggtggggtagactttcgagaaaatcggttACCATGGTGAGCAAGGGCGAGGAG-30) and cxcr4a_HA2_kanR_rev (50-gtgttgggctggggcgccgggggcttcagctcggtttccatcatgttataTCAGAAGAACTCGTCA-AG AAGGCG-30). The Cerulean cassette was amplied by PCR from pCS2 Cerulean_

kanR with the primers cxcl12a_HA1_gfp_fw (50-cacagttgctcctggat-tctacacagtgcggatc tcttcttcacactgcaAC-CATG-GTGAGCAAGGGCGAGGAG-30) and cxcl12a_HA2_ kanR_rev (50-gcatgaatggcgaccgccatcagagcgactactacgatcactttgagatc-TCAGAAGAAC TCGTCAAGAAGGCG -30); homology to the BAC vector is depicted in lower case. Tg(cxcl12bBAC:YFP)mu105 was generated as previously described25. BAC DNA was isolated by Midiprep (Invitrogen) and injected at 100 pg per embryo together with 50 pg per embryo of tol2 transposase mRNA into wild-type embryos.

The Tg(Cry.kop.HSP:mutSDF1a.mCherry.globin30UTR)mu4 sh line was generated using the Tol2 transposon system. The transgene contains the HSP70/4 promoter (AF158020.1, GI:7108904) cloned upstream of the Danio rerio Cxcl12a coding sequence (FJ915063.1, GI:239596165) mutated in a way rendering it resistant for the morpholino oligonucleotide (ATGgacttgaaggtcatcg) and fused in frame to the mCherry open-reading frame (AB971706.1 GI:662033815). The Xenopus laevis globin30UTR (J00978.1 GI:214209) was cloned downstream of the mCherry sequence.

In vivo imaging of adult sh. The in vivo imaging of adult sh was carried out as described with the following modications51. Tg(i1a:nEGFPy7; 0.8t1:RFPhu5333)

sh were anaesthetized in 0.02% tricaine until they stopped swimming, transferred to the home-made chamber for live imaging, and immobilized by covering the trunk and caudal n with 1% agarose. Afterwards, sh were orally administered with 126 mg l 1 tricaine in sh water at the speed of 5.5 ml min 1. We inserted a

Silicone tubing (ID mm, OD 6 mm) into the sh mouth for tricaine delivery. The speed of tricaine delivery was controlled by a peristaltic pump (ISM-795C, ISMATEC). The removal of extra tricaine solution in the imaging chamber was achieved by connecting it to a uid aspiration system for cell culture. Image acquisition was done for a maximum of 24 h every 15 min using a Leica SP5 confocal microscope equipped with a 20 dipping lens. Confocal stacks and movies were

assembled using Imaris software (Bitplane). The Linear Stack Alignment with SIFT plugin of ImageJ (NIH) was used for aligning image stacks. The MtrackJ plugin as implemented in ImageJ was used to label movies.

Confocal microscopy and imaging processing. Fin regenerates were embedded in 1% low melting point agarose (Invitrogen) and imaged immediately after amputation. Images were acquired using a Leica SP5 confocal microscope and a Zeiss LSM780 confocal microscope. Maximum Projection images were generated with Imaris software (Bitplane). ImageJ (NIH) and Volocity 6.1 (PerkinElmer) were used to quantify cell number, vessel area and vessel length. We chose the third n ray from the dorsal and/or ventral edge for our measurements. A region of interest (40 250 mm, width height) in the centre of the growing vessel in the

distal end of regenerating n rays at 3 d.p.a. and two regions of interest of the same size in bifurcating n rays from 5 d.p.a. onwards were measured. In total, the n vasculature of at least ten n rays from at least ve sh was analysed for the each animal group of different regeneration stages. The MannWhitney non-parametric test as implemented in Prism 6.0b (Graphpad) was used to analyse the data.

Quantication of endothelial cell proliferation in zebrash ns by in vivo live imaging. Dividing endothelial cells were counted over 24 h in three independent movies each for wild-type and cxcr4aum20 mutants. Differences in proliferative behaviour between wild types and mutants were analysed in venous (lateral vein and medial vein combined) and arterial cell populations. The unpaired t-test as implemented in Prism 6.0b (Graphpad) was used for statistic analysis; signicance (*Po0.05, **Po0.01) in unpaired t-test; NS not signicant.

Heat-shock experiments. Heat shocks were carried out every 12 h on 14 consecutive days. For this purpose, sh were placed in system water, which was heated gradually for about 1015 min from 28 C to 37 C in a standard waterbath. Subsequently, sh were exposed to 37 C for 1 h, before gradual return to 28 C.

In situ hybridization. Whole-mount in situ hybridization was carried out as described27. Previously described probes were cxcr4a27, cxcl12b27 and cxcl12a52. Probes were generated from plasmid DNA. The plasmid containing cxcr4a was digested with NotI. The plasmids containing cxcl12a or cxcl12b were digested with NcoI. Sp6 was used to generate DIG-labelled antisense RNA for all three probes. DNA template for in vitro synthesis of cxcr4a sense probe was amplied from pCRII-cxcr4a by PCR. The forward primer 50-GCTTGATTTAGGTGACACTAT

AGAATTATCGGGAACGGACTGG-30 containing SP6 promoter and reverse primer 50-AGGCGTACAGGATCGGG-30 were used for PCR amplication. Proteinase K (30 mg ml 1) was used to permeabilize 2 d.p.a. n regenerates for 20 min at room temperature before proceeding to the in situ hybridization with aforementioned probes. Images were acquired using a Leica M205 C Microscope and a Zeiss Axio Imager microscope.

Blastomere transplantation. Cell transplantation was performed as described40. About 40 cells were transplanted from donor embryos to the margin of host embryos at sphere stage. The endothelial cell contribution of transplanted cells was assessed by visualization of EGFP and RFP expression. Adult sh containing EGFP and RFP expressing endothelial cells in the n vasculature were selected for analysis.

Genetic lineage tracing of endothelial tip cells. Esm1(BAC)-iCreERT2 transgenics22 were bred into a R26-tomato-EGFP21 reporter background. Cre activity in newborn mice was induced by a single intraperitoneal injection of 50 mg 4-hydroxy tamoxifen solution (Sigma, H7904; 1 mg ml 1 in ethanol/peanut oil) at 12, 24 or 48 h before analysis at postnatal stage P6.

Retina immunostaining for genetic lineage labelling. For retina staining, eyes were dissected and xed in 4% PFA for 2 h at room temperature. Retinas were dissected, permeabilized and blocked in 1% BSA (Sigma, A4378-25G) and 0.3% Triton X-100 2 h at room temperature with agitation. Biotinylated isolectin B4 (Vector, B-1205, Griffonia simlicifolia lectin I; 1:25) in blocking buffer was added and incubated overnight at 4 C with agitation. Next day, Retinas were washed three times in PBS and incubated with Alexa-Fluor-coupled streptavidin 647 (Invitrogen, 1:100) in blocking buffer together with GFP Alexa-Fluor-coupled 488 antibody (A21311, Invitrogen, 1:300) for 2 h at RT. Retinas were at-mounted using Fluromount-G (SouthernBiotech, 0100-01) and images were taken with a Leica SP5 confocal microscope. Volocity software (PerkinElmer) was used for image processing and quantitative analysis.

EdU labelling. Esm1-iCreERT2 /T, R26mTmG /T double heterozygous mice were injected intragastric with 50 ml of 4-hydroxytamoxifen solution(0.25 mg ml 1; H7904 Sigma), at P2. Fifty microlitres of freshly prepared EdU nucleotides (2 mg ml 1 in PBS) was administered intraperitoneally at P6 and pups were dissected after 2 h.

Whole-mount retina immunostaining and EdU detection. Retina immunostaining was performed according to Pitulescu et al.53 with some modications. Whole eyes were xed for 10 min at RT followed by 1 h on ice, with freshly prepared 4%PFA/ PBS. Retinas were dissected and blocked/permeabilized (1% BSA, 0.3% Triton, PBS) for 30 min at RT. After rinsing twice with modied Pblec buffer (1 mM CaCl2, 1 mM

MgCl2, 1 mM MnCl2, 0.4% Triton X-100 in PBS), retinas were incubated overnight at 4 C with biotinylated Griffonia simplicifolia lectin I (isolectin B4) (1:50, VectorLabs, B-1205) and the following primary antibodies: rabbit anti-Erg (1:200, Santa-Cruz, sc-353) and chicken anti-GFP (1:300, Aves Labs, GFP-1010). On the next day, retinas were washed for 20 min in blocking buffer diluted once with PBS and three times (10 min per wash) in PBS. Retinas were then incubated for 2 h with CFTM405M-streptavidin antibody (1:100, Biotrend, 29033) or Alexa Fluor 546 streptavidin-conjugated (1:100, Invitrogen, S11225) and the following species-specic secondary antibodies: Alexa Fluor 488-donkey anti-chicken (1:500, Jackson ImmunoResearch Lab., 703-545-155), Alexa Fluor 647-goat anti-rabbit (1:500, Invitrogen, A21244) or Alexa Fluor 594-donkey anti-rabbit (1:500, Invitrogen, A21207). Retinas were then washed as described above. To detect EdU incorporation Click-IT EdU detection reactions were performed according to the manufacturer (Life Technologies, C103339 or C10340), using either Alexa Fluor 594 or 647 azide. Retinas were washed twice in PBS and at-mounted on glass microscope slides using Fluoromount-G (Southern Biotech, 0100-01).

References

1. Eilken, H. M. & Adams, R. H. Dynamics of endothelial cell behavior in sprouting angiogenesis. Curr. Opin. Cell. Biol. 22, 617625 (2010).

2. Herbert, S. P. & Stainier, D. Y. Molecular control of endothelial cell behaviour during blood vessel morphogenesis. Nat. Rev. Mol. Cell. Biol. 12, 551564 (2011).

10 NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications

NATURE COMMUNICATIONS | DOI: 10.1038/ncomms6758 ARTICLE

3. Potente, M., Gerhardt, H. & Carmeliet, P. Basic and therapeutic aspects of angiogenesis. Cell 146, 873887 (2011).

4. Wacker, A. & Gerhardt, H. Endothelial development taking shape. Curr. Opin. Cell. Biol. 23, 676685 (2011).

5. DiPietro, L. A. Angiogenesis and scar formation in healing wounds. Curr. Opin. Rheumatol. 25, 8791 (2013).

6. Isogai, S., Horiguchi, M. & Weinstein, B. M. The vascular anatomy of the developing zebrash: an atlas of embryonic and early larval development. Dev. Biol. 230, 278301 (2001).

7. Mukouyama, Y. S., Shin, D., Britsch, S., Taniguchi, M. & Anderson, D. J. Sensory nerves determine the pattern of arterial differentiation and blood vessel branching in the skin. Cell 109, 693705 (2002).

8. Stahl, A. et al. The mouse retina as an angiogenesis model. Invest. Ophthalmol. Vis. Sci. 51, 28132826 (2010).

9. Huang, C. C., Lawson, N. D., Weinstein, B. M. & Johnson, S. L. reg6 is required for branching morphogenesis during blood vessel regeneration in zebrash caudal ns. Dev. Biol. 264, 263274 (2003).

10. Machado, M. J. et al. Dynamics of angiogenesis during wound healing: a coupled in vivo and in silico study. Microcirculation 18, 183197 (2011).

11. Siekmann, A. F., Affolter, M. & Belting, H. G. The tip cell concept 10 years after: New players tune in for a common theme. Exp. Cell. Res. 319, 12551263 (2013).

12. Geudens, I. & Gerhardt, H. Coordinating cell behaviour during blood vessel formation. Development 138, 45694583 (2011).

13. Jakobsson, L. et al. Endothelial cells dynamically compete for the tip cell position during angiogenic sprouting. Nat. Cell Biol. 12, 943953 (2010).

14. Arima, S. et al. Angiogenic morphogenesis driven by dynamic and heterogeneous collective endothelial cell movement. Development 138, 47634776 (2011).

15. Bussmann, J., Wolfe, S. A. & Siekmann, A. F. Arterial-venous network formation during brain vascularization involves hemodynamic regulation of chemokine signalling. Development 138, 17171726 (2011).

16. Ellertsdottir, E. et al. Vascular morphogenesis in the zebrash embryo. Dev. Biol. 341, 5665 (2010).

17. Fujita, M. et al. Assembly and patterning of the vascular network of the vertebrate hindbrain. Development 138, 17051715 (2011).

18. Lawson, N. D. & Weinstein, B. M. In vivo imaging of embryonic vascular development using transgenic zebrash. Dev. Biol. 248, 307318 (2002).

19. Bussmann, J. et al. Arteries provide essential guidance cues for lymphatic endothelial cells in the zebrash trunk. Development 137, 26532657 (2010).

20. Roman, B. L. et al. Disruption of acvrl1 increases endothelial cell number in zebrash cranial vessels. Development 129, 30093019 (2002).

21. Muzumdar, M. D., Tasic, B., Miyamichi, K., Li, L. & Luo, L. A global double-uorescent Cre reporter mouse. Genesis 45, 593605 (2007).

22. Rocha, S. F. et al. Esm1 modulates endothelial tip cell behavior and vascular permeability by enhancing VEGF bioavailability. Circ. Res. 115, 581590 (2014).

23. del Toro, R. et al. Identication and functional analysis of endothelial tip cell-enriched genes. Blood 116, 40254033 (2010).

24. Strasser, G. A., Kaminker, J. S. & Tessier-Lavigne, M. Microarray analysis of retinal endothelial tip cells identies CXCR4 as a mediator of tip cell morphology and branching. Blood 115, 51025110 (2010).

25. Bussmann, J. & Schulte-Merker, S. Rapid BAC selection for tol2-mediated transgenesis in zebrash. Development 138, 43274332 (2011).

26. Montes, G. S., Becerra, J., Toledo, O. M., Gordilho, M. A. & Junqueira, L. C. Fine structure and histochemistry of the tail n ray in teleosts. Histochemistry 75, 363376 (1982).

27. Siekmann, A. F., Standley, C., Fogarty, K. E., Wolfe, S. A. & Lawson, N. D. Chemokine signaling guides regional patterning of the rst embryonic artery. Gene Dev. 23, 22722277 (2009).

28. Valentin, G., Haas, P. & Gilmour, D. The chemokine SDF1a coordinates tissue migration through the spatially restricted activation of Cxcr7 and Cxcr4b. Curr. Biol. 17, 10261031 (2007).

29. Rorth, P. Fellow travellers: emergent properties of collective cell migration. EMBO Rep. 13, 984991 (2012).

30. Raz, E. & Mahabaleshwar, H. Chemokine signaling in embryonic cell migration: a sheye view. Development 136, 12231229 (2009).

31. Bayliss, P. E. et al. Chemical modulation of receptor signaling inhibits regenerative angiogenesis in adult zebrash. Nat. Chem. Biol. 2, 265273 (2006).

32. Gerhardt, H. et al. VEGF guides angiogenic sprouting utilizing endothelial tip cell lopodia. J. Cell Biol. 161, 11631177 (2003).

33. Stratman, A. N., Davis, M. J. & Davis, G. E. VEGF and FGF prime vascular tube morphogenesis and sprouting directed by hematopoietic stem cell cytokines. Blood 117, 37093719 (2011).

34. Benedito, R. & Hellstrom, M. Notch as a hub for signaling in angiogenesis. Exp. Cell Res. 319, 12811288 (2013).

35. Li, W. et al. Peripheral nerve-derived CXCL12 and VEGF-A regulate the patterning of arterial vessel branching in developing limb skin. Dev. Cell 24, 359371 (2013).

36. Mukouyama, Y. S., Gerber, H. P., Ferrara, N., Gu, C. & Anderson, D. J. Peripheral nerve-derived VEGF promotes arterial differentiation via neuropilin 1-mediated positive feedback. Development 132, 941952 (2005).

37. Ehling, M., Adams, S., Benedito, R. & Adams, R. H. Notch controls retinal blood vessel maturation and quiescence. Development 140, 30513061 (2013).

38. Blum, Y. et al. Complex cell rearrangements during intersegmental vessel sprouting and vessel fusion in the zebrash embryo. Dev. Biol. 316, 312322 (2008).39. Nicoli, S., Knyphausen, C. P., Zhu, L. J., Lakshmanan, A. & Lawson, N. D. miR-221 is required for endothelial tip cell behaviors during vascular development. Dev. Cell 22, 418429 (2012).

40. Siekmann, A. F. & Lawson, N. D. Notch signalling limits angiogenic cell behaviour in developing zebrash arteries. Nature 445, 781784 (2007).

41. Sallusto, F. & Baggiolini, M. Chemokines and leukocyte trafc. Nat. Immunol. 9, 949952 (2008).

42. Kiefer, F. & Siekmann, A. F. The role of chemokines and their receptors in angiogenesis. Cell Mol. Life Sci. 68, 28112830 (2011).

43. Nair, S. & Schilling, T. F. Chemokine signaling controls endodermal migration during zebrash gastrulation. Science 322, 8992 (2008).

44. Tiveron, M. C. & Cremer, H. CXCL12/CXCR4 signalling in neuronal cell migration. Curr. Opin. Neurobiol. 18, 237244 (2008).

45. Boldajipour, B. et al. Control of chemokine-guided cell migration by ligand sequestration. Cell 132, 463473 (2008).

46. Dona, E. et al. Directional tissue migration through a self-generated chemokine gradient. Nature 503, 285289 (2013).

47. Venkiteswaran, G. et al. Generation and dynamics of an endogenous, self-generated signaling gradient across a migrating tissue. Cell 155, 674687 (2013).

48. Chitnis, A. B., Nogare, D. D. & Matsuda, M. Building the posterior lateral line system in zebrash. Dev. Neurobiol. 72, 234255 (2012).

49. Haas, P. & Gilmour, D. Chemokine signaling mediates self-organizing tissue migration in the zebrash lateral line. Dev. Cell 10, 673680 (2006).

50. Poss, K. D., Shen, J. & Keating, M. T. Induction of lef1 during zebrash n regeneration. Dev. Dyn. 219, 282286 (2000).

51. Knopf, F. et al. Bone regenerates via dedifferentiation of osteoblasts in the zebrash n. Dev. Cell 20, 713724 (2011).

52. Miyasaka, N., Knaut, H. & Yoshihara, Y. Cxcl12/Cxcr4 chemokine signaling is required for placode assembly and sensory axon pathnding in the zebrash olfactory system. Development 134, 24592468 (2007).

53. Pitulescu, M. E., Schmidt, I., Benedito, R. & Adams, R. H. Inducible gene targeting in the neonatal vasculature and analysis of retinal angiogenesis in mice. Nat. Protoc. 5, 15181534 (2010).

Acknowledgements

This work was funded by the Max Planck Society (A.F.S.), the Deutsche Forschungsgemeinschaft (DFG SI-1374/3-1; A.F.S.), the Sonderforschungsbereich (SFB) 629 an ERC advanced grant (268806 - CellMig; E.R.) and an ERC starting grant (260794-ZebrashAngio; A.F.S.). This work was supported by the Deutsche Forschungsgemeinschaft (DFG) Cells-in-Motion Cluster of Excellence (EXC 1003-CIM), University of Mnster, Germany. Jeroen Bussmann was supported by a European Molecular Biology Organization (EMBO) long-term fellowship.

Author contributions

C.X., R.H.A. and A.F.S. planned the experiments. C.X., I.S. and M.P. carried out the experiments. C.X., S.S.H., I.S., M.P., R.H.A. and A.F.S. analysed the data. S.F.R. generated the esm1(BAC)-iCreERT2 transgenic mouse line. J.B. generated the Tg(cxcr4aBA

C:YFP)mu104 transgenic zebrash line. D.M. and E.R. contributed the Tg(Cry.-kop.HSP:mutSDF1a.mCherry.globin30UTR)mu4 sh line. C.X. and A.F.S. wrote the paper.

All authors commented on the manuscript.

Additional information

Supplementary Information accompanies this paper at http://www.nature.com/naturecommunications

Web End =http://www.nature.com/ http://www.nature.com/naturecommunications

Web End =naturecommunications

Competing nancial interests: The authors declare no competing nancial interests.

Reprints and permission information is available online at http://npg.nature.com/reprintsandpermissions/

Web End =http://npg.nature.com/ http://npg.nature.com/reprintsandpermissions/

Web End =reprintsandpermissions/

How to cite this article: Xu, C. et al. Arteries are formed by vein-derived endothelial tip cells. Nat. Commun. 5:5758 doi: 10.1038/ncomms6758 (2014).

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the articles Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Web End =http://creativecommons.org/licenses/by/4.0/

NATURE COMMUNICATIONS | 5:5758 | DOI: 10.1038/ncomms6758 | http://www.nature.com/naturecommunications

Web End =www.nature.com/naturecommunications 11

Word count: 9248

Show less

Abstract

Translate

Tissue vascularization entails the formation of a blood vessel plexus, which remodels into arteries and veins. Here we show, by using time-lapse imaging of zebrafish fin regeneration and genetic lineage tracing of endothelial cells in the mouse retina, that vein-derived endothelial tip cells contribute to emerging arteries. Our movies uncover that arterial-fated tip cells change migration direction and migrate backwards within the expanding vascular plexus. This behaviour critically depends on chemokine receptor cxcr4a function. We show that the relevant Cxcr4a ligand Cxcl12a selectively accumulates in newly forming bone tissue even when ubiquitously overexpressed, pointing towards a tissue-intrinsic mode of chemokine gradient formation. Furthermore, we find that cxcr4a mutant cells can contribute to developing arteries when in association with wild-type cells, suggesting collective migration of endothelial cells. Together, our findings reveal specific cell migratory behaviours in the developing blood vessel plexus and uncover a conserved mode of artery formation.

Details

Title

Arteries are formed by vein-derived endothelial tip cells

Author

Xu, Cong; Hasan, Sana S; Schmidt, Inga; Rocha, Susana F; Pitulescu, Mara E; Bussmann, Jeroen; Meyen, Dana; Raz, Erez; Adams, Ralf H; Siekmann, Arndt F

Pages

5758

Publication year

2014

Publication date

Dec 2014

Publisher

Nature Publishing Group

e-ISSN

20411723

Source type

Scholarly Journal

Language of publication

English

DOI

https://doi.org/10.1038/ncomms6758

ProQuest document ID

1636195362

Arteries are formed by vein-derived endothelial tip cells

Jump to:

Full text

Abstract

Details

Suggested sources