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Received 22 Oct 2012 | Accepted 26 Mar 2013 | Published 7 May 2013

Caveolae are abundant in endothelial cells and are thought to have important roles in endothelial cell biology. The cavin proteins are key components of caveolae, and are expressed at varied amounts in different tissues. Here we use knockout mice to determine the roles of cavins 2 and 3 in caveolar morphogenesis in vivo. Deletion of cavin 2 causes loss of endothelial caveolae in lung and adipose tissue, but has no effect on the abundance of endothelial caveolae in heart and other tissues. Changes in the morphology of endothelium in cavin 2 null mice correlate with changes in caveolar abundance. Cavin 3 is not required for making caveolae in the tissues examined. Cavin 2 determines the size of cavin complexes, and acts to shape caveolae. Cavin 1, however, is essential for normal oligomerization of caveolin 1. Our data reveal that endothelial caveolae are heterogeneous, and identify cavin 2 as a determinant of this heterogeneity.

DOI: 10.1038/ncomms2808 OPEN

Deletion of cavin genes reveals tissue-specic mechanisms for morphogenesis of endothelial caveolae

Carsten Gram Hansen1,w, Elena Shvets1,*, Gillian Howard1,*, Kirsi Riento1 & Benjamin James Nichols1

1 MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK. w Present address: Sanford Consortium for Regenerative Medicine and UCSD, 2880 Torrey Pines Scenic Drive, La Jolla, California 92037, USA. * These authors contributed equally to this work. Correspondence and requests for materials should be addressed to B.J.N. (email: mailto:[email protected]

Web End [email protected] ).

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Caveolae have a range of functions, playing important roles in adipocyte metabolism and lipid homoeostasis, in cellular mechanosensation, and in endothelial cell

biology, as well as other processes14. Caveolae comprise around 20% of the surface of continuous microvascular endothelium57, and are linked to endothelial permeability by several different observations. Electron microscopy suggests that budding of caveolae from one side of the endothelial cell and fusion at the other side may constitute a mechanism for endothelial transcytosis810. Imaging of antibodies against caveolar proteins reveals that these antibodies are efciently pumped from blood to surrounding tissue11. Endothelial pores share common protein components with caveolae, particularly the protein PV-1 (refs 1214). Further experiments reveal a role for caveolae in the regulation of endothelial nitric oxide synthase signalling, which impacts directly on the permeability state of endothelial paracellular junctions3,15,16. The molecular cell biology underlying these processes remains largely unknown.

Recent research has identied a protein family, the cavins, which are crucial for the formation of caveolae1723. Previously, the only proteins established in this process were the caveolins. There are three caveolins in mammals. Caveolins 1 and 2 are abundant in endothelium and adipose tissue, and are expressed at lower levels in other tissues excluding striated muscle. Caveolin 3 is restricted to striated muscle24. Intriguingly, caveolin 1 alone can generate caveolae-like membrane vesicles in a completely heterologous system25, so it is likely that the expression of the cavins provides additional functional and regulatory complexity. There are four cavins in mammals. Cavins 1 to 3 are widely expressed, while cavin 4 is, like caveolin 3, expressed only in striated muscle26. In this paper we use the cavin names, but it should be noted that these are not the standard gene names for this family (cavin 1 Ptrf, cavin 2 Sdpr, cavin 3 Prkcdbp,

cavin 4 Murc. Cavin 3 is also frequently referred to as SRBC17).

The cavin proteins form hetero-oligomeric complexes18,27. They are expressed at different abundances in various tissues, leading to the hypothesis that the presence of different complements of cavin proteins could generate differences between caveolae in diverse tissues or cell types17,27. Direct evidence to support this hypothesis has been lacking.

Knockout mice for the caveolin 1 or cavin 1 genes have been generated previously2831, and display a similar range of complex lipodistrophic and other metabolic defects that may be linked to the role of caveolae in adipocytes1,28,32,33. Endothelial barrier function and other cardiovascular parameters have yet to be fully analysed in the cavin 1 / mice, but there are several reports that endothelial permeability to albumin is increased in caveolin 1 / mice3,9,3436. This implies that, if caveolae do indeed mediate endothelial transcytosis, compensatory mechanisms must exist to actually increase albumin efux from blood vessels in their absence. In agreement with this, there is evidence for opening of endothelial tight junctions in the lung of caveolin 1 / mice3,34,36.

In this paper, we report the generation of cavin 2 / and cavin 3 / mice, and analyse cells and tissues from these mice alongside those from caveolin 1 / and cavin 1 / strains.

We have used biochemical, imaging and electron microscopy methods to study the requirements for different cavins in the formation of morphologically dened caveolae in the endothelium of different tissues, and in cultured endothelial cells. We have also used complementary approaches to assess alterations in endothelial ultrastructure in the knockout mice. We found that cavin 3 does not appear to be needed for generating endothelial caveolae, and the morphology of the endothelium in cavin 3 / mice is normal. Cavin 2, however, has an important role specically in generating caveolae in lung

and fat endothelia. The apparent size of the protein complexes into which cavins assemble is smaller in the lung and fat compared with other tissues. Cavin 2 is responsible for determining the size or stability of cavin complexes, as deletion of cavin 2 actually increases the apparent size of cavin complexes in the lung. In both the endothelium of the lung and in cultured lung endothelial cells, the residual caveolae detected in the absence of cavin 2 have a reduced depth. Moreover, in cavin 2 / cells other caveolar components such as cavin 1 and caveolin 1 are detected in at regions of the plasma membrane and shallow caveolae. We conclude that endothelial caveolae in different tissues are heterogeneous, that cavin 2 has an important role in generating such heterogeneity, and that the role of cavin 2 in caveolar morphogenesis is directly linked to determining the membrane shape of caveolae.

ResultsGeneration of cavins 2 / and 3 / mice. We imported mice lacking caveolin 1 (ref. 30), and backcrossed them for seven generations onto the strain C57Bl/6. We imported mice lacking cavin 1, already on the C57Bl/6 background28. We generated mice lacking cavin 2 and mice lacking cavin 3, using C57Bl/6 embryonic stem cells (Supplementary Fig. S1), and following germ-line transmission of the null mutation backcrossed these onto C57Bl/6 for four generations. As one would predict given the previous characterization of caveolin 1 / and cavin 1 /

mice, all four null strains were viable and fertile with no gross phenotypes28,30,31,37. However, in crosses where both parents were heterozygous for cavin 1 there was a signicant deviation from the predicted frequency of homozygous knockout pups (In heterozygous x heterozygous crosses percentage of homozygous knockout pups at weaning was 26% for cavin 2 (N 195), 29% for cavin 3 (N 235), 13% for cavin 1 (N 137)

and 25% for caveolin 1 (N 106)).

Western blotting of a range of tissues from the knockout mice and congenic controls conrmed that the caveolin 1, cavin 1, cavin 2 and cavin 3 proteins are indeed absent in the relevant strains (Fig. 1 and Supplementary Fig. S2). Changes in cavin 1 and caveolin 2 expression in caveolin 1 / mice and caveolin 1 and 2 expression in cavin 1 / mice were consistent with previous reports20,27,38. Deletion of cavin 1 caused loss of cavin 2 and 3 proteins, but cavin 2 / and cavin 3 / mice had unaltered levels of cavin 1 and caveolin 1 (Fig. 1). Similarly, cavin 2 levels were not altered when cavin 3 was deleted. However, there was consistent upregulation of cavin 3 in cavin 2 / mice across all tissues examined. This was the case even in tissues, such as kidney, spleen, testis, brain and muscle, where cavin 2 could not be detected by western blotting (Fig. 1 and Supplementary Fig. S2). These data from western blotting of tissues from the different knockout mice show that cavins 2 and 3 are not stably expressed in the absence of cavin 1 or caveolin 1, conrm that the ratio between the different cavins is markedly different in different tissues27 and demonstrate that deletion of cavin 2 or cavin 3 does not reduce the levels of other caveolar proteins. In addition, western blotting with antibodies against the recently identied caveolar protein EHD2 (refs 23, 3941) showed that this protein is also expressed at reduced levels in caveolin 1 / and cavin 1 / mice, thereby providing direct evidence that it is likely to be linked to caveolar function in vivo.

The different tissue distributions of the cavins could, in principle, reect either expression in different cell types or changes in relative abundance within the same cell type. In the case of cavin 4 the former is the case, as cavin 4 is expressed predominantly in myocytes of striated muscle26,27,42. In the case of cavin 3 the latter is the case, as cavin 3 and caveolin 1 clearly

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NATURE COMMUNICATIONS | DOI: 10.1038/ncomms2808 ARTICLE

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Figure 1 | Protein expression levels in cavin 13 and caveolin 1 knockout mice. Tissues from mice with the indicated genotypes were analysed by western blotting, using antibodies as shown. Note that all samples were obtained and analysed in duplicate. Blots for the lung, heart, fat and liver, and for skeletal muscle and brain, were processed and exposed to lm simultaneously, so that the intensity of the bands for each individual protein is meaningfully comparable and gives information on the relative abundance of each protein in the different tissues shown. Ponceau staining of the membranes used for blotting is included to demonstrate equal total protein loading. More tissue types are analysed in Supplementary Fig. S2.

co-localize in several tissues19. The distribution of cavins 1 and 2 within tissues has not been studied in detail. Indirect immunouorescent labelling of tissue sections with antibodies against cavin 1, cavin 2 and caveolin 1 revealed that in all tissues examined cavin 1, cavin 2 and caveolin 1 co-localize extensively. Cavin 1 and cavin 2 antibodies gave highly specic labelling, as judged using knockout tissue as a negative control (Supplementary Fig. S3). In the heart and in adipose tissue caveolin 1, cavin 1 and cavin 2 are found predominantly in endothelial cells (Fig. 2). In subsequent experiments, we focused on the role of cavins 1, 2 and 3 in generating caveolae in endothelia.

Quantication of the abundance of endothelial caveolae. We carried out a survey of the abundance of caveolae in micro-vascular endothelia in different tissues from control, cavin 1 / , cavin 2 / , cavin 3 / and caveolin 1 / mice, aiming to correlate potential changes in caveolar abundance with the differential expression of cavin proteins. Initially, we examined micrographs by eye and scored the abundance of endothelial caveolae using an arbitrary scale (Supplementary Fig. S4A). This was done with randomized samples and completely blind to the genotype of each individual sample. This initial study suggested that: (1) caveolae are largely absent in caveolin 1 / and cavin 1 / tissues, as one would predict2831; (2) cavin 3 is

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Figure 2 | Distribution of cavins 1 and 2 in different tissues. Sections of the tissues shown were labelled using indirect immunouorescence, with antibodies against caveolin 1, cavin 1 and cavin 2. The black and white panels show the areas denoted with a dashed box, the signals from the three antibodies being separated to allow visualization of co-localization. Bars are all 20 mm.

not essential for formation of endothelial caveolae in any of the tissues examined; (3) the effects of deletion of cavin 2 are not uniform across endothelia from different tissues, for example, in lung endothelia of cavin 2 / mice there were very few structures morphologically identiable as caveolae, whereas in the heart and muscle, however, there was no noticeable difference between control and cavin 2 / mice (Supplementary Fig. S4A).

As these observations provide direct evidence for different requirements for caveolar morphogenesis in different types of endothelial cell, we sought to conrm them in a quantitative manner. We focused on continuous microvascular endothelium of the lung and the heart. As cavin 3 expression increases in cavin 2 / mice (Fig. 1, Supplementary Fig. S2), we investigated potential functional redundancy or compensatory effects on caveolar abundance between these two cavins by breeding cavin 2 / cavin 3 / double knockout mice. Multiple electron micrographs were obtained (Fig. 3a) and the number of caveolae counted. This was done in control, caveolin 1 / , cavin 2 /

and cavin 3 / mice, as well as for cavin 2 / cavin 3 / double knockouts (Fig. 3a,b). The results conrmed that deletion of cavin 3 does not signicantly (using an unpaired t-test) alter the abundance of caveolae. Additionally, cavin 2 is not required for generating caveolae in the heart microvascular endothelia, but in the cavin 2 / lung samples the abundance of caveolae in microvascular endothelium was greatly reduced. The abundance of caveolae in the lung and the heart from cavin 2 / cavin 3 / double knockouts was the same as was observed for cavin 2 / samples in both cases, so the differential effects on caveolar abundance in the heart and lung endothelium observed when cavin 2 is deleted are not due to compensatory or functionally redundant processes requiring cavin 3.

The residual caveolar membrane invaginations in cavin 2 / and cavin 2 / cavin 3 / lung endothelium frequently appeared more shallow than those observed in control samples (Fig. 3a,c). Morphometric analysis of the depth of these invaginations in cavin 2 / and cavin 2 / cavin 3 / samples conrmed that they are indeed shallower than control caveolae, and revealed that the effect of deleting cavin 2 was the same as deleting both cavin 2 and cavin 3 simultaneously (Fig. 3d). Deletion of cavin 2, or deletion of cavin 2 and cavin 3 simultaneously, had no effect on the size or shape of caveolae in the heart endothelium (Fig. 3d). The data show, therefore, that cavin 2 is not required for generating caveolae in the heart microvascular endothelium, but that in the microvascular endothelium of lung the deletion of cavin 2 causes a pronounced reduction in the abundance of caveolae. The loss of caveolae in cavin 2 / lung is less severe than that observed in caveolin 1 /

samples, and the shallow caveolar invaginations seen in cavin 2 / samples from these tissues are not seen in caveolin 1 / samples.

This latter observation argues that the invaginations are indeed caveolar in origin, rather than representing a potential separate type of invagination induced by loss of caveolae.

The size of cavin complexes varies between tissues. Cavin proteins assemble into hetero-oligomeric complexes, and these complexes are likely to be central to cavin function17,27,43. In HeLa cells, cavin complexes can be isolated as a single peak on sucrose velocity gradients following solubilization in 0.5% Triton X100 (ref. 43). We applied essentially the same protocol to study the size of cavin complexes in different tissues. The cavins were found in highmolecular-weight complexes, and in all tissues cofractionated with each other (Fig. 4a (ref. 43)). However, the fractionation behaviour of cavin complexes was not the same in all tissues examined. In the heart and the kidney, the cavin proteins peaked at a sucrose density of 2022%. In both lung and fat the cavin complexes had a markedly smaller size, peaking at a sucrose density of 1012% (Fig. 4a,b). Use of puried 40S and 60S ribosomal subunit as standards indicated that the cavin complexes are a little less than 40S in lung and fat, and around 60S in the other tissues (Fig. 4c). These data imply that there are biochemical differences between cavin complexes in different tissues.

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Figure 3 | Cavin 2 is required for generating endothelial caveolae in lung but not heart. (a) Cavin 2 / lung endothelium lacks caveolae, but cavin 2 / heart endothelium has the same abundance of caveolae as congenic controls. Representative electron micrographs are shown, with the relevant genotype indicated. Note the shallow membrane invaginations in cavin 2 / lung and cavin 2 / cavin 3 / lung, arrowed. Bars, 500 nm. (b)

Quantication of caveolae in the heart and lung microvascular endothelium in tissues from congenic control, caveolin 1 / , cavin 2 / , cavin 3 / , and cavin 2 / cavin 3 / mice. Multiple electron micrographs were obtained for each tissue, and both the number of caveolae and total length of plasma membrane present were quantied in each image. Caveolae were counted as omega-shaped membrane proles open at the cell surface. N415, bars are s.e.m., P-values were calculated using an unpaired t-test. (c) Higher-resolution images comparing the depth of membrane invaginations seen in cavin 2 / lung endothelium with caveolae from control lung endothelium. Note that these invaginations are included as morphologically dened caveolae in the quantication shown in b, and are much less frequent than caveolae in control samples, and are not seen in caveolin 1 / mice. Bars, 100 nm.

(d) Quantication of the depth of caveolae in the lung and the heart microvascular endothelium from cavin 2 / , cavin 3 / , and cavin 2 / cavin 3 / mice. Depth was measured in electron micrographs from the caveolar opening as illustrated in c. N4100.

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Figure 4 | Cavin complexes have different apparent sizes in different tissues. (a) Western blots of fractions from sucrose density gradients.

Both the fraction number, used for the plots in b, and the experimentally (by refractometer) determined sucrose density from each fraction are shown. Fractions from each tissue (heart, kidney, lung and fat) were probed with antibodies against cavin 1, cavin 2 and cavin 3. (b) Densitometry from western blots as in a, to allow distribution of cavin proteins to be compared in different tissues. Bars represent s.e.m., values are means from three separate experiments. Key indicates which prole is from each tissue. (c) Densitometry from Coomassie blue-stained gels of fractions from velocity gradientsof samples containing puried ribosomal subunits, and aldolase, as standards.

Lung and fat contain high levels of cavin 2 (Fig. 1). We quantied the abundance of caveolae in cavin 2 / adipocytes and cavin 2 / endothelium within adipose tissue and found that in both cases there was a loss of caveolae as seen in cavin 2 / lung endothelium, while deletion of cavin 3 did not effect caveolar abundance (Supplementary Fig. S4B). With these observations in mind, we asked whether the decrease in apparent size of cavin complexes in the lung and fat could be explained by the activity of cavin 2. We carried out sucrose velocity gradient fractionation as for Fig. 4, analysing the lung

and the heart from cavin 2 / , cavin 3 / and cavin 2 / cavin 3 / mice, and used western blotting to follow the distribution of cavin 1 on the gradients. In the heart, there was no large change in distribution of cavin 1 in any of the knockout samples, although in the cases of cavin 3 / and cavin 2 /

cavin 3 / samples the size of the complexes containing cavin 1 was slightly reduced (Fig. 5a). This is what one would predict, as cavins 2 and 3 are likely to be present in those complexes along with cavin 1. In the lung, however, there was a marked increase in the size of cavin 1-containing complexes in cavin 2 / samples

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Figure 5 | Cavin 2 controls the size of cavin complexes. (a) Densitometry from western blots of fractions from sucrose velocity gradients as inFig. 4, comparing the distribution of cavin 1 complexes in the heart from control, cavin 2 / , cavin 3 / and cavin 2 / cavin 3 / mice. Colour key indicates which prole is from each tissue/genotype. Note that the control data are reproduced in all three panelsvalues shown are means from three experiments, bars represent s.e.m. (b) Densitometry from western blots of fractions from sucrose velocity gradients as in Fig. 4, comparing the distribution of cavin 1 complexes in lung from control, cavin 2 / , cavin 3 / and cavin 2 / cavin 3 / mice. Colour key indicates which prole is from each tissue/genotype. Note that the control data are reproduced in all three panelsvalues shown are means from three experiments, bars represent s.e.m.

(c) Densitometry from western blots of fractions from sucrose velocity gradients, comparing the distribution of cavin 1 complexes from control and caveolin 1 / lung and heart tissues. Colour key indicates which prole is from each genotype. Values shown are means from three experiments, bars represent s.e.m. Note that the absolute abundance of cavin 1 in caveolin 1 / tissues is much less than controls, and all data are normalized to show relative abundance in different fractions, peak fraction 1.

(Fig. 4b), so that the prole of cavin 1 in cavin 2 / lungs resembled that observed in control heart. There was a slight decrease in the size of cavin 1 complexes in cavin 3 / samples (Fig. 4b), and cavin 2 / cavin 3 / samples contained cavin 1 complexes at increased size relative to controls, but this increase was less pronounced than when cavin 2 alone was absent (Fig. 4b). These data imply that cavin 2 has a specic role in controlling the size or stability of cavin complexes, that expression of cavin 2 reduces the size or stability of these complexes and that this activity of cavin 2 may account for the variation in the apparent size of cavin complexes on sucrose gradients observed between the lung and the heart.

To ascertain whether caveolin 1 has an effect on the different distribution of cavin complexes in the lung and the heart, we analysed these tissues using sucrose velocity gradients from control and caveolin 1 / mice and western blotting for cavin 1 (Fig. 5c). Comparing caveolin 1 / with controls, cavin 1 was still found in large complexes, the distribution of these complexes peaked at approximately the same point in the gradient, and cavin 1-containing complexes still had a clearly different apparent size between the lung and the heart (Fig. 5c). Therefore, although there was some decrease in the abundance of cavin 1 in the densest fractions from caveolin 1 / samples from both tissues, it is likely that cavin complexes form differently in the heart and the lung independently from caveolin 1.

The role of cavin 2 in lung endothelial cells. One complication in the interpretation of the sucrose gradient data outlined above is that there is a range of cell types, each potentially with a different complement of cavins and caveolins, in each tissue. To gain further insight into the role of cavin 2 specically in the lung endothelial cells, where it has an important role in the morphogenesis of caveolae, we established cultures of endothelial cells isolated from the lung of mice with different genotypes. In the cavin 2 / cells, there was a reduction in the abundance of caveolae and the residual caveolae were shallower than controls (Fig. 6ac). There was no change in the abundance of caveolae in cavin 3 / cells (Fig. 6b). Cavin complexes, analysed using sucrose velocity gradients as previously, and detected by blotting of fractions with antibodies against cavins 1 and 3, had a similar size in the cultured control cells as in control lung tissue (Fig. 6d,e: compare with Fig. 4b). Crucially, however, in the cavin 2 / cells cavin complexes were signicantly larger than in controls, in fact resembling those found in the heart in size (Fig. 6d,e: compare with Fig. 4b). Cavin 1 cofractionated with cavin 3 in both control and cavin 2 / cells (Fig. 6d), so the increase in size of complexes upon deletion of cavin 2 is likely to represent the behaviour of bona de cavin complexes rather than aggregation or other aberrant behaviour. Therefore, the changes in abundance and shape of caveolae, and in the apparent size of cavin complexes, in cavin knockout lung endothelial cells

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ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms2808

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Figure 6 | Deletion of cavin 2 increases the apparent size of cavin complexes. (a) Electron micrographs comparing the morphology of caveolae from control and cavin 2 / lung endothelial cells. Note that the abundance of caveolar invaginations in the cavin 2 / sample is over-represented in these images selected to show examples of typical morphology. Bars, 100 nm. (b) Quantication of the abundance of morphological caveolae in the lung endothelial cells from control, caveolin 1 / , cavin 2 / and cavin 3 / mice. N 12 cells, each reconstructed from 2030 individual micrographs

tracing the cell perimeter. Bars are s.e.m. (c) Quantication of the depth of caveolar membrane invaginations seen in cavin 2 / lung endothelial cells in culture. Depth was measured in electron micrographs as illustrated in a. N4200. (d) Western blots using antibodies against cavins 2 and 3 of fractions from sucrose velocity gradients analysing extracts from control and cavin 2 / lung endothelial cells. (e) Densitometry showing the distribution of cavin 1 on gradients as in d. Values shown are means from three separate experiments, bars are s.e.m.

recapitulate those observed in the lung in vivo. The data conrm that cavin 2 is indeed responsible for the reduced size of cavin complexes in the lung endothelial cells.

We used indirect immunouorescence and confocal microscopy to further characterize the mis-formation of caveolae in cavin 2 / lung endothelial cells, by following co-localization between caveolin 1 and cavin 1. In control and cavin 3 / cells, caveolin 1 and cavin 1 co-localized in membrane puncta typical of caveolae (Fig. 7a). In cavin 1 / cells, caveolin 1 staining was weak and diffuse, consistent with the reduced size of caveolin 1 complexes in sucrose gradients (Fig. 7b), and previous observations suggesting that caveolin 1 does not form stable oligomers in the absence of cavin 1 (refs 20,21,43). In cavin 2 / cells, however, caveolin 1 and cavin 1 co-localized, and could not be distinguished from controls (Fig. 7a), and there was no decrease in the size of caveolin 1 complexes in sucrose gradients. In contrast, deletion of cavin 1 caused a pronounced reduction in the size of caveolin 1 complexes (Fig. 7b).

So as to conrm that there is no change in the amount of caveolin 1 and cavin 1 present at the plasma membrane in

cavin 2 / cells, the amount of each protein present in total internal reection images of the basal plasma membrane was quantied (Fig. 7c). The amount of caveolin 1 and cavin 1 was the same in control, cavin 2 / and cavin 3 / cells. As predicted, there was much less caveolin 1 present in cavin 1 / cells than in controls (Fig. 7c). These ndings, coupled with our data showing that the number of morphological caveolae in the cavin 2 / cells is around half that observed in controls (Fig. 6b), and that the residual caveolae in the cavin 2 / cells are signicantly shallower than in controls (Fig. 6c), implies that a number of the apparently normal caveolin 1/cavin 1 puncta seen by immunouorescence in cavin 2 / cells are likely to in fact correspond to at regions of membrane or aberrantly shallow caveolae. We sought to conrm this inference, using pre-embedding immuno-labelling with caveolin 1 or cavin 1 antibodies and electron microscopy. We could clearly observe the presence of caveolin 1 and cavin 1 in both control caveolae and in the smaller structures seen in cavin 2 / cells (Fig. 7d). In addition, immuno-EM revealed cavin 1 and caveolin 1 in at membrane patches in the cavin 2 / cells (Fig. 7d). These ndings demonstrate that cavin 2 is involved in the morphogenesis of caveolar membranes.

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Figure 7 | Deletion of cavin 2 causes attening of caveolae without perturbing oligomerization of caveolin 1. (a) Indirect immunouorescent staining of cultured lung endothelial cells (MLEC) from control, cavin 1 / , cavin 2 / and cavin 3 / mice, using anti-caveolin-1 and anti-cavin-1 antibodies.

The top panels show staining for caveolin 1 alone, the lower panels dual colour labelling with both antibodies. Note that there is much less caveolin 1 in cavin 1 / cells than in the other genotypes, and the microscope gain settings were increased when imaging cavin 1 / cells. Bars, 5 mm.

(b) Densitometry from blots of fractions from sucrose velocity gradients analysing the distribution of caveolin 1 in control, cavin 1 / , cavin 2 / and cavin 3 / lung endothelial cells. Note that the absolute abundance of caveolin 1 in cavin 1 / cells is much lower than in other genotypes (see c), data here are normalized so that peak abundance on the gradient 1. Means of three experiments, bars s.e.m., colour key indicates genotype.

(c) Quantication of the amount of plasma membrane associated labelling observed with antibodies against caveolin 1 and cavin 1 in the lung endothleial cells with genotypes shown in the key. Images were acquired with total internal reection illumination to image the basal B100 nm of cells. Fluorescence intensities were all normalized so that mean from control cells 1, values are mean of 420 cells, bars s.e.m. (d) Pre-embedding immuno-electron

microscopy of control and cavin 2 / cells with caveolin 1 or cavin 1 antibodies. Secondary antibodies were coupled to nano-gold and silver enhancement was used to aid detection of these secondary antibodies. Bars, 100 nm.

Deletion of cavin 2 perturbs the lung endothelial morphology. The results presented above show that cavin 2 is involved in the formation of caveolae and modulation of cavin complex formation in the endothelium of some tissues, such as the lung, but not others, such as the heart. This predicts that cavin 2 should be required for at least some of the functions of caveolae in lung but not heart endothelium. We examined the ultrastructural

morphology of the lung microvascular endothelium, seeking to ascertain whether there are specic changes in caveolin 1 / , cavin 1 / and cavin 2 / animals, where the abundance of caveolae is reduced. In conventional electron micrographs of samples from caveolin 1 / cavin 1 / and cavin 2 /

lung we observed, in B5% of capillary cross-sections, gaps in the normally continuous endothelium (Fig. 8a). In the areas

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a Control

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Figure 8 | cavin 2 / endothelial morphology resembles that of caveolin 1 / mice in the lung but is normal in the heart. (a) Electron micrographs of capillaries from the lung of mice with the genotypes indicated. Red arrows indicate gaps between endothelial cells. L, lumen of capillary; En, endothelial cell; Ep, epithelial cell; J, endothelial tight junction; RBC, red blood cell (not present in all images). Bars, 5 mm. Tissue was taken from 20- to 25-week-old female mice with the genotypes indicated. (b) Perfusion xation with Lanthanum ions produces electron-dense deposits on cell surfaces accessible from the vascular lumen. Tissue was taken from 20- to 25-week-old female mice with the genotypes indicated. Transverse sections of microvascular capillaries from the heart are shown, lanthanum staining is restricted to the luminal face of blood vessels in all samples exceptcaveolin 1 / and cavin 1 / . In these two genotypes lanthanum deposits are observed between cells and outside of the endothelial layer,as showed in the magnied regions indicated with red dashed boxes and highlighted with arrows. Bars, 5 mm.

containing endothelial gaps neither endothelial cells nor the adjacent epithelial cell layer were well attached to the intervening connective tissue (Fig. 8a). Gaps or discontinuities between endothelial cells may represent a more severe consequence of the previously reported reduction in the size of endothelial tight junctions in caveolin 1 / lung36. The gaps are not an artifact induced by vascular pressure changes during perfusion xation, as they were also observed in tissue samples xed without perfusion (Supplementary Fig. S5). In contrast to cavin 2 / , cavin 3 / lungs were essentially the same as those from congenic controls (Fig. 8a), conrming that the phenotype is linked to absence of caveolae and that in the lung cavin 2 /

pheno-copies cavin 1 / and caveolin 1 / .

We next examined endothelial morphology in the heart. Conventional electron microscopy did not reveal obvious changes, beyond the presence or absence of caveolae, in any of the genotypes we examined (not shown). As conventional electron microscopy does not report directly on the functional status of tight junctions, we sought a more sensitive electron-microscopy-based assay for altered endothelial permeability. We perfused mice with xative containing lanthanum ions. Lanthanum forms electron-dense precipitates on polysaccharides present in the glycocalyx, and so perfusion xation in the presence of lanthanum provides a means of discerning whether the lumen of capillaries is continuous with the extravascular space44,45. Lanthanum deposits clearly highlighted the capillary

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luminal face of endothelial cells in the heart (Fig. 8b). In the case of caveolin 1 / and cavin 1 / mice, additional lanthanum deposits were observed in the interstitial space between the endothelium and adjacent cardiomyocytes, providing direct evidence for increased endothelial permeability (Fig. 8b). This was not the case in cavin 2 / mice, or in controls and cavin 3 / . Surprisingly then, in both the lung and heart cavin 3 does not appear to be required for making endothelial caveolae, or for the function of caveolae in terms of maintaining endothelial morphology and hence barrier function. Endothelial phenotypes of cavin 2 / mice resemble those of congenic controls in the heart, but those of cavin 1 / and caveolin 1 /

in the lung. This means that cavin 2 is likely to be required for the function of endothelial caveolae in the lung but not in the heart.

DiscussionThe identication of the cavin proteins as key components of caveolae with differing tissue distributions27 suggested the hypothesis that expression of different complements of cavin proteins confers different properties on caveolae in different tissues17. The assembly of a set of mouse strains lacking genes for caveolin 1, cavin 1, cavin 2 and cavin 3 has allowed us to test this hypothesis. Three main lines of evidence conrm that endothelial caveolae are heterogeneous between tissues; the differential requirements for cavin 2 expression in caveolar morphogenesis in different endothelia, the variation in the apparent sizes of cavin complexes in different tissues and the differential functional consequences of deletion of cavin 2 in terms of altered endothelial morphology.

Our data reveal that cavin 2 is required for generating caveolae in some types of endothelium but not others, and that cavin 3 is dispensable for formation of endothelial caveolae. Therefore, in some contexts, but not in others, cavin 1 and caveolin 1 may be sufcient for generating caveolae27. We speculate that the explanation for this apparent paradox lies in the different nature of the complexes into which cavins can assemble. In tissues where cavin 2 is needed for making caveolae, cavin 1 runs on sucrose gradients as much smaller complexes than in other tissues. It is possible that this reduced apparent size in fact represents reduced stability of complexes during extraction and analysis, rather than differences in the size of cavin complexes in situ. In either eventuality, however, the conclusion that the properties of cavin complexes are different in different tissues remains valid. Information on the structure of different cavin complexes, how assembly of the complexes is controlled, and whether further tissue-specic components are present, is lacking. It is also possible that association of further, non-cavin, proteins could directly inuence the size of cavin complexes.

Despite the uncertainties outlined above, the data do provide clear evidence that the cavin proteins have quite different roles. Cavin 1 is required to mediate or maintain the normal oligomerization of caveolin 1 (refs 18,20,21), and our experiments reveal that cavin 1 co-localizes with oligomerized caveolin 1 in cells that lack cavin 2 even when this does not result in formation of morphological caveolae with normal efciency, as is the case in the lung endothelial cells. Cavin 2 is, therefore, required for caveolar morphogenesis in specic contexts. Consistent with our ndings in cultured lung endothelial cells lacking cavin 2, attened or shallow caveolae are observed in cavin 2 short hairpin RNA-treated adipocytes33. Unlike cavin 1, cavin 2 does not directly stabilize caveolin 1 oligomers. Rather, cavin 2 has a strong effect on formation of cavin complexes, the presence of cavin 2 reducing the size or stability of these complexes.

Although the cavin proteins do clearly form a single protein family17, our data argue that they are not functionally interchangeable. There is no detectable expression of cavin 4 in endothelial cells when cavin 2 or cavin 3 are deleted, so cavin 4 is unlikely to compensate for the lack of other cavins in endothelial cells. Even in the case of cavin 3 in cavin 2 / animals, where there is some upregulation of protein expression, our data on the quantication of caveolar abundance in cavin 2 / cavin 3 /

double knockout animals implies that cavin 3 does not compensate, in this respect at least, for the lack of cavin 2. It is possible that specic aspects of caveolar function are dependent on expression of cavin 3. Intriguingly, these functions would then probably not require the characteristic morphology of caveolae.

None of our observations using electron microscopy report the complete absence of caveolae. This is at least in part likely to be because we have relied on a purely morphological denition of caveolae, and ask-shaped invaginations of the plasma membrane may be generated in several waysfor example, a vesicle in the process of fusion with the plasma membrane could be ultrastructurally very similar to caveolin-positive caveolae. It also remains possible that there is an alternative mechanism for generating caveolae46. Previous studies on the role of cavin 2 in generating caveolae report slightly more severe loss of caveolae, as well as reduced expression of caveolin 1, in cultured adipocytes or HeLa cells following short hairpin RNA-mediated knockdown than we observe in vivo18,27,33. The reason for this is unclear, but potential explanations include differences between cell type and the possibility that partial loss of cavin 2 causes different effects from complete loss of the protein.

Cardiovascular phenotypes in mutant animals lacking caveolae indicate a role in endothelial permeability3,11,35,36. These phenotypes are likely to be due to functions for caveolae as transcytotic vesicles10, as regulators of eNOS activity3, and as sensors of mechanical stress2,47,48. Our data showing that endothelial caveolae differ biochemically and are generated in different ways between tissues suggest a mechanism by which alternative aspects of caveolar function may be carried out by these morphologically quite uniform structures. The endothelium of different tissues is highly heterogeneous in terms of both morphology and function7,49,50, and cavin 2 is one of the molecular components that generates this heterogeneity.

Methods

Mouse genetics and husbandry. To produce cavin 2 or cavin 3 gene knockout mice, targeted embryonic stem cells (clone names 11065A-H7 and 11448A-D8, respectively) generated by the trans-NIH Knock-Out Mouse Project (KOMP) were obtained from the KOMP Repository (http://www.komp.org

Web End =www.komp.org). The ES cells were injected into separate blastocysts derived from C57BL6 mice and implanted into pseudo-pregnant females using standard techniques. Resulting heterozygous /

chimeric animals were backcrossed to C57Bl/6. Cavin 1 (PTRF) knockout animals were obtained from the Jackson Laboratories (http://www.jax.org

Web End =www.jax.org) and have previously been described28. Likewise, caveolin 1 knockout animals30 were obtained from the Jackson Laboratories and backcrossed onto C57Bl/6 background for seven generations.

Loss of the genomic locus of interest was conrmed by PCR (Supplementary Fig. S1). Genotyping was carried out by a multiplex PCR, primers used are shown in Supplementary Table S1. Changes in gene expression were conrmed by quantitative PCR (lack of messenger RNA, not shown) and western blotting (Fig. 1 and Supplementary Fig. S2).

Mice used in all experiments were sex and age matched, kept in individually ventilated cages in pathogen-free conditions and fed a standard chow (from Special Diets Services). All animal experiments were undertaken with the approval of the UK Home Ofce and local MRC-LMB Ethical Review Committee.

DNA constructs and antibodies. All DNA constructs have been described previously18,41. Sources for antibodies were as follows: rabbit polyclonal anti-PTRF (Cavin1) (ab48824), rabbit polyclonal anti-PRKCDBP (Cavin3) (ab83913), rabbit polyclonal anti-Caveolin3 (ab2912) and goat polyclonal anti-EHD2 (ab23935) were all from Abcam. Polyclonal rabbit anti-caveolin 1 (Ab 610059) and mouse monoclonal anti caveolin 2 (Ab 610685) were both from BD Biosciences).

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Monoclonal antibodies raised against caveolin 1 were generously provided by Jrgen Vinten (The Panum Institute, University of Copenhagen, Denmark)51. Polyclonal Goat anti SDPR (Cavin2) is raised against the N-terminal part of the protein. Polyclonal Rabbit anti SDPR (Cavin2) is raised against the C-terminal part of the protein. Polyclonal rabbit anti-MURC (Cavin4) is raised againstthe C-terminal part of the protein. HRP-conjugated secondary antibodieswere from DAKO and the ECL western blotting detection kit was fromGE Healthcare.

Light microscopy. Mice were culled by cervical dislocation, tissues were dissected and immediately frozen on dry ice and stored at 80 C until processed. Frozen

sections were cut on a microtome (Leica CM3050S). Sections were transferred onto frosted microscope slides (Thermo Scientic) and air dried for 2 h, xed in 4% paraformaldehyde (PFA) in PBS for 1 h, washed, labelled with the appropriate antibodies, and nally overlaid with 40,6-diamidino-2-phenylindole Fluoromount-

G (SouthernBiotech). Images were acquired with a Plan-Apochromat 40 1.3oil

DIC M27 objective on a Zeiss 780 confocal microscope with standard lter settings. The gamma was increased in red/green overlay images to allow visualization of co-localization.

Electron microscopy. Perfusion xation of mice was carried out under anaesthesia, via injection into the left ventricle and cutting of the right atrial chamber. Blood was ushed away using an initial perfusate of Hanks buffered salt solution heparin.

Standard transmission electron microscopy. Tissues were then perfused with xative containing 2.0% PFA, 2.5% glutaraldehyde (GA) in 0.1 M sodium cacodylate buffer pH 7.4. The heart, liver, kidney, fat, lung and abdominal muscle were then rapidly dissected and placed in fresh xative. The same protocol was followed for tissues xed without perfusion, except that the initial xative was supplemented with 4 mM CaCl2. Following several buffer washes, tissues were post xed in 1% osmium tetroxide in 0.1 M sodium cacodylate buffer for 1 h at 4 C. Tissues were then enbloc stained with 2% uranyl acetate in 30% ethanol and further dehydrated in an increasing ethanol series, followed by propylene oxide and inltration and embedding in CY212 resin. Sections were counterstained with Reynolds Lead Citrate and viewed on a Philips 208 microscope operated at 80 kV. Quantication of caveolae in endothelium was carried out as described previously18.

Lanthanum tracer studies. Following perfusion with Hanks buffered salt solution heparin, mice were perfused with xative containing lanthanum

chloride (3.0% PFA, 2.5% GA and 1% lanthanum chloride in 0.1 M pipes buffer pH 7.2 at room temperature (RT) for 15 min, followed by the same xative minus the LaCl for several hours. Tissue specimens were then washed in 0.1 M pipes buffer, and then post-xed in 1% osmium tetroxide in 0.1 M sodium cacodylate for 1 h on ice, enbloc stained with 7% uranyl acetate in water for 2 h at 4 C, and dehydrated and processed as for as above.

Immuno-labelling. Endothelial cells were grown on gelatine-coated glass bottom Petri dishes (MatTek) and xed in 4% PFA in 0.1 M phosphate buffer pH 7.4 overnight at 4 C. After several buffer washes, followed by inactivation of reactive aldehyde groups using 0.1% sodium borohydride in phosphate buffer for 15 mins, cells were permeabilized using 0.03% saponin in 20 mM phosphate buffer, 150 mM sodium chloride for 30 mins. Cells were incubated in normal goat serum (Aurion) for 40 min before incubation in rabbit anti-caveolin 1 antibody used at 1:200 for4.5 h at RT. After thorough washing, cells were incubated with 1:200 dilution of goat anti rabbit ultrasmall gold (Aurion) overnight at 4 C. After washing cells were xed with 2% GA in 0.1 M phosphate buffer for 30 min, washed with distilled water followed by silver enhancement of gold using R-Gent SE-EM (Aurion) reagents. Cells were then post xed with 0.5% osmium tetroxide in 0.1 M phosphate buffer on ice for 15 mins. Cells were then dehydrated in an ascending ethanol series and embedded in CY212 resin. Ultrathin sections were stained with saturated aqueous uranyl acetate and Reynolds lead citrate and examined using a Philips 208 EM operated at 80 kV.

Sucrose velocity gradients. We used a protocol based on that of Hayer et al.43 Different tissues were washed in PBS and approximately 0.05 g of tissue was homogenized using a Dounce homogenizer in 1 ml of 0.5% Triton X100 in 100 mM NaCl, 20 mM TrisHCl pH 7.4, 5 mM EDTA, supplemented with Complete protease inhibitors (Roche). The samples were next incubated in RT for 20 min. Post-nuclear supernatant (PNS) was prepared by a 6-min centrifugation at 1,100 g. 800 ml of PNS was loaded onto step gradient of 40, 35, 30, 25, 20 and 10% sucrose containing 0.5% TX100, 20 mM TrisHCl pH 7.4, 100 mM NaCl, 5 mM EDTA and protease inhibitors. For analysis of extracts from endothelial cells, one Petri dish containing cells was solubilized in 1 ml 0.5% TX100, 20 mM TrisHCl pH 8,300 mM NaCl, 5 mM EDTA. PNS was loaded onto a step gradient of 40, 35, 30, 25, 20 and 10% sucrose containing 0.5% TX100, 20 mM TrisHCl pH 8, 300 mM NaCl, 5 mM EDTA.

The gradients were centrifuged at 4C in SW40 rotor (Beckman) for 270 min at 245,000 g with slow acceleration and deceleration. Twelve 900 ml fractions were collected from the top of the gradient, and densities of the fractions were calculated from the refractive indices. From each fraction, 200 ml samples were precipitated using 10% trichloroacetic acid and pellets were analysed by SDSpolyacrylamide gel electrophoresis/western blot. Puried ribosomal samples for calibration were a kind gift from Alexey Amunts (MRC-LMB).

Western blotting. Mice were culled by cervical dislocation, tissues were removed and immediately frozen on dry ice and either processed the same day or stored at

80 C. Tissues were homogenized with an IKA-Werke homogenizer in 0.5 ml RIPA buffer supplemented with protease inhibitor tablets (Roche). The homogenized tissues were left rolling at 4 C for 3 h, and the homogenate was cleared by centrifugation at 16,000 g for 10 min. The supernatant, or samples from fractionation as described above, were mixed with reducing sample buffer, boiled and run on pre-cast 420% Tris-glycine gels (Invitrogen). The gels were blotted using a semi-dry blotter (Bio-Rad) and the membrane blocked in a PBS solution containing 4% dried skimmed milk powder and incubated with the appropriate antibodies, washed and incubated with secondary antibodies (DAKO). The blots were developed using Immobilon (Millipore) onto Fuji Super RX X-ray lms.

Endothelial cell culture. Mice were killed by cervical dislocation, lungs dissected, nely chopped with a scalpel blade and digested in collagenase for 2 h. The cell mixture was run through a 70-mm nylon cell strainer (BD Falcon), spun down and suspended in mixed medium (50% low-glucose DMEM (Gibco), 50% F12 Nut Mix (Gibco) supplemented with 20% FCS and 100 mg ml 1 endothelial cell mitogen (Serotec). The cell mixture was then seeded onto one 0.1% gelatin-coated chamber (Sigma) of a six-well plate per lung equivalent. The medium was changed the following day. After 46 days in culture the cells were trypsinized and endothelial cells were immuno-isolated using rat anti-mouse CD102 antibodies (BD Pharmigen) and dynabeads (Dynal Biotech). Isolated endothelial cells were hereafter plated on 0.1% gelatin-coated plastic. Endothelial cell purity was assessed by morphology at conuency, and positive expression of VE-Cadherin.

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Acknowledgements

NIH grants to Velocigene at Regeneron Inc. (U01HG004085) and the CSD Consortium (U01HG004080) funded the generation of gene-targeted ES cells for 8,500 genes in the KOMP Program, and archived and distributed by the KOMP Repository at UC Davis and CHORI (U42RR024244). E.S. was funded by EMBO. C.G.H. was funded by the Lundbeck Foundation. We thank all LMB biomedical and transgenic services personnel for expert help in mouse transgenesis and breeding, Vernon Smith for carrying out perfusions, Grant Otto for advice on endothelial cell culture and Alexey Amunts (MRCLMB) for providing the ribosome preparations used as sedimentation standards.

Author contributions

C.G.H. generated knockout mice and carried out analysis of tissues and cultured endothelial cells. E.S. carried out gradient fractionation of cavin complexes from tissues. G.H. prepared and analysed all samples for electron microscopy. K.R. managed mouse experiments. B.J.N. wrote the manuscript and assisted in quantication of caveolae.

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

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

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How to cite this article: Hansen, C. G. et al. Deletion of cavin genes reveals tissue-specic mechanisms for morphogenesis of endothelial caveolae. Nat. Commun. 4:1831 doi: 10.1038/ncomms2808 (2013).

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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NATURE COMMUNICATIONS | 4:1831 | DOI: 10.1038/ncomms2808 | http://www.nature.com/naturecommunications

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Title

Deletion of cavin genes reveals tissue-specific mechanisms for morphogenesis of endothelial caveolae

Author

Hansen, Carsten Gram; Shvets, Elena; Howard, Gillian; Riento, Kirsi; Nichols, Benjamin James

Pages

1831

Publication year

2013

Publication date

May 2013

Publisher

Nature Publishing Group

e-ISSN

20411723

Source type

Scholarly Journal

Language of publication

English

DOI

https://doi.org/10.1038/ncomms2808

ProQuest document ID

1355894838

Deletion of cavin genes reveals tissue-specific mechanisms for morphogenesis of endothelial caveolae

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