Pro-apoptotic Bax is the major and Bak an auxiliary effector in cytokine deprivation-induced mast cell apoptosis

Abstract

The process of apoptosis in immune cells like mast cells is essential to regain homeostasis after an inflammatory response. The intrinsic pathway of apoptosis is ultimately controlled by the pro-apoptotic Bcl-2 family members Bax and Bak, which upon activation oligomerize to cause increased permeabilization of the mitochondria outer membrane leading to cell death. We examined the role of Bax and Bak in cytokine deprivation-induced apoptosis in mast cells using connective tissue-like mast cells and mucosal-like mast cells derived from bax ^-/- , bak^-/- and bax^-/- bak^-/- mice. Although both Bax and Bak were expressed at readily detectable protein levels, we found a major role for Bax in mediating mast cell apoptosis induced by cytokine deprivation. We analyzed cell viability by propidium iodide exclusion and flow cytometry after deprivation of vital cytokines for each mast cell population. Upon cytokine withdrawal, bak ^-/- mast cells died at a similar rate as wild type, whereas bax^-/- and bax^-/- bak^-/- mast cells were partially or completely resistant to apoptosis, respectively. The total resistance seen in bax^-/- bak^-/- mast cells is comparable with mast cells deficient of both pro-apoptotic Bim and Puma or mast cells overexpressing anti-apoptotic Bcl-2. These results show that Bax has a predominant and Bak a minor role in cytokine deprivation-induced apoptosis in both connective tissue-like and mucosal-like mast cells.

Citation: Cell Death and Disease (2010) , e43; doi:10.1038/cddis.2010.20

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Pro-apoptotic Bax is the major and Bak an auxiliary effector in cytokine deprivation-induced mastcell apoptosis

M Karlberg1, M Ekoff1, V Labi2, A Strasser3, D Huang3 and G Nilsson*,1

The process of apoptosis in immune cells like mast cells is essential to regain homeostasis after an inammatory response. The intrinsic pathway of apoptosis is ultimately controlled by the pro-apoptotic Bcl-2 family members Bax and Bak, which upon activation oligomerize to cause increased permeabilization of the mitochondria outer membrane leading to cell death. We examined the role of Bax and Bak in cytokine deprivation-induced apoptosis in mast cells using connective tissue-like mast cells and mucosal-like mast cells derived from bax / , bak / and bax / bak / mice. Although both Bax and Bak were expressed at readily detectable protein levels, we found a major role for Bax in mediating mast cell apoptosis induced by cytokine deprivation. We analyzed cell viability by propidium iodide exclusion and ow cytometry after deprivation of vital cytokines for each mast cell population. Upon cytokine withdrawal, bak / mast cells died at a similar rate as wild type, whereas bax / and bax / bak / mast cells were partially or completely resistant to apoptosis, respectively. The total resistance seen in bax / bak / mast cells is comparable with mast cells decient of both pro-apoptotic Bim and Puma or mast cells overexpressing anti-apoptotic Bcl-2. These results show that Bax has a predominant and Bak a minor role in cytokine deprivation-induced apoptosis in both connective tissue-like and mucosal-like mast cells.

Cell Death and Disease (2010) 1, e43; doi:http://dx.doi.org/10.1038/cddis.2010.20

Web End =10.1038/cddis.2010.20 ; published online 13 May 2010

Subject Category: Immunity

This is an open-access article distributed underthe terms of the Creative CommonsAttributionLicense, which permits distribution and reproduction in any medium, provided the original author and source are credited. This license does not permit commercial exploitation without specic permission.

Apoptosis is a genetically programmed mechanism for induction of cell death. During an allergic inammation, the number of inammatory immune cells including mast cells increase at site. During the resolution phase and termination of the inammation, the process of apoptotic cell death is critical to regain cellular and tissue homeostasis.1

The intrinsic pathway of apoptosis is activated by stimuli such as growth factor deprivation or cell stress, including DNA damage2 and is tightly regulated by interactions between pro- and anti-apoptotic members of the Bcl-2 family. The proapoptotic BH3-only proteins comprising Bim, Bad, Noxa and Puma are essential for initiation of apoptosis signaling. This group of proteins activates the pro-apoptotic effector proteins Bax and Bak indirectly by binding to the anti-apoptotic Bcl-2 family members (Bcl-2, Bcl-xL, Bcl-w, Mcl-1 and B-1/A1) and thereby titrate them away from Bax and Bak.3 Whether the activation of Bax and Bak occurs only indirectly is, however, actively debated. A model of direct binding and activation of Bax and Bak by the promiscuous BH3-only proteins Bid, Bim

and possibly Puma has also been suggested.47 Activation of Bax and Bak causes permeabilization of the mitochondrial outer membrane, leading to release of cytochrome c, activation of caspase-9 and ultimately cell demolition.8

Activation of mast cells by aggregation of the high afnity receptor for IgE, FceRI, is a key event in allergic reactions leading to degranulation and release of pro-inammatory mediators. Connective tissue-like mast cells (CTLMC) but not mucosal-like mast cells (MLMC) withstand the degranulation process by activation-induced survival,9 a process in which the induction and function of the pro-survival protein A1 is crucial.10 In addition, other Bcl-2 family members such as the pro-survival protein Bcl-XL but also the pro-apoptotic protein

Bim are upregulated by FceRI aggregation in mast cells.11

Experiments with gene-targeted mice have shown that loss of either Bim11 or Puma12 renders mast cells partially resistant to cytokine deprivation-induced apoptosis. Experiments using RNAi-mediated knockdown of gene expression showed that the pro-survival Bcl-2 family member Mcl-1 is critical for

1Department of Medicine, Karolinska Institutet, Stockholm, Sweden; 2Division of Developmental Immunology, Biocenter, Innsbruck Medical University, Innsbruck, Austria and 3The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia*Corresponding author: G Nilsson, Department of Medicine, Karolinska Institutet, Clinical Immunology and Allergy Unit, KS L2:04, Stockholm 171 76, Sweden.

Tel: [phone]; Fax: [phone]; E-mail: mailto:[email protected]

Web End [email protected]

Keywords: Bcl-2; BH3-only; indirect apoptosis modelAbbreviations: Bcl-2, B-cell lymphoma-2; Bax, Bcl-2-associated X protein; Bak, Bcl-2 -antagonist/killer-1; BH3, Bcl-2 homology domain 3; Bim, Bcl-2-interacting mediator of cell death; Noxa, Latin for damage; Puma, p53 upregulated modulator of apoptosis; Bcl-XL, Bcl-2 like protein extra large; Bcl-w, Bcl-2 like 2; Mcl-1, myeloid cell leukemia sequence 1; B-1/A1, Bcl-2 related protein A1; tBid, truncated BH3-interacting domain death agonist; CTLMC, connective tissue like mast cell; MLMC, mucosal like mast cell; FceRI, Fc epsilon receptor I; SCF, stem cell factor; MEF, mouse embryonic broblast; RPA, RNase protection assay; PI, propidium iodide

Received 22.12.09; revised 24.3.10; accepted 07.4.10; Edited by D Bano

Bax dependency in mast cell apoptosis M Karlberg et al

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sustained survival of transformed mast cells.13 In this study,

we have examined the role of the two pro-apoptotic effector proteins Bax and Bak in mast cells, using cells decient in Bax, Bak or both. We found that Bax has a more prominent role than Bak in cytokine deprivation-induced apoptosis in both CTLMC and MLMC.

Results

Characterization of in vitro-produced bax / bak / MLMC and CTLMC. To characterize bax / bak / MLMC and CTLMC, we examined their surface expression of Kit and the high-afnity IgE receptor FceRI. Immunouorescent staining with specic Abs and ow cytometric analysis

showed that mast cell populations lacking Bax and Bak expressed levels of Kit and FceRI similar to their wt counterpart (Figure 1a). We then compared the response of wt and bax / bak / MLMC and CTLMC, respectively, to FceRI crosslinking measuring degranulation using a b-hexosaminidase assay. In response to FceRI cross-linking both wt and bax / bak / MLMC and CTLMC, respectively, responded by degranulation to a similar magnitude (Figure 1b). These results show that the in vitro-produced cells resembled primary mast cells, as conrmed by toluidine blue staining of cytoplasmic granules (data not shown), expression of FceRI and c-Kit. In these respects, wt mast cells and mast cells lacking Bax and Bak were indistinguishable.

Figure 1 (a) Expression of the receptors Kit and FceRI on the cell surface of wt and bax / bak / CTLMC and MLMC as examined by ow cytometry. The colors black and gray represents wt and bax / bak / mast cells, respectively. A dashed line represents the staining with an isotype-matched control Ab, whereas the lled line represents staining with Abs for either Kit or FceRI. b-hexosaminidase release upon FceRI cross-linking of wt and bax / bak / (dko) CTLMC and MLMC, respectively (b). One representative of two independent experiments is presented

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Figure 2 (a) Expression of mRNA for Bcl-2 members was analyzed using RPA. Extracted mRNA, 2 mg per sample, was analyzed using a mAPO-2 multi-probe template according to the RiboQuant System protocol. Presented is one representative of two independent experiments. (b) The expression levels of pro-survival bcl-2 family members were quantied in relation to control l32 and gapdh using a phosphor-imager device. Data is presented as fold difference compared with wild type of two different sets of RPA. (c) Both Bax and Bak proteins are expressed in wt CTLMC and control cells, mouse embryonic broblasts (MEF). Mast cells were either resting or activated by IgE receptor cross-linking for 5 h. One representative of three independent experiments is presented

Expression of Bax and Bak in mast cells. Mast cells were differentiated from mouse embryonic fetal livers. After 4 weeks in culture, pure cell cultures of CTLMC were obtained. We then started by examining the protein and mRNA expression of the two effector proteins Bax and Bak. Analyzing mRNA expression of Bax and Bak in CTLMC by RNase protection assay (RPA) revealed a more abundant expression of bax compared with bak (Figure 2a). Moreover, loss of either bax or bak did not cause any compensatory alteration in the expression of the pro-survival genes bcl-w, a1, bcl-xL or bcl-2 (Figure 2b). On protein level, both Bax and

Bak were detected in wild-type mast cells, although the levels of Bak appeared to be lower than the levels of Bax. Expectedly, no Bax or Bak protein was seen in mast cells from respectively knock-out as well as from double-decient mast cells (Figure 2c). Furthermore, we investigated if activation of mast cells through FceRI not only alters the expression of pro-survival proteins and BH3-only proteins,10,11 but also the effector proteins Bax and Bak.

We could observe a minor upregulating effect on Bak but no prominent effect on Bax (Figure 2c), suggesting that IgE receptor activation primarily controls mast cell survival by regulating the levels and function of survival proteins and BH3-only proteins and not the effector proteins.

Loss of Bax protects mast cells from cytokine deprivation-induced apoptosis. Although both Bax and Bak have been shown to have largely overlapping functions in several cell types (e.g., lymphoid cells14,15), it has also

been reported that one of these proteins can have the dominant role. For example, Bax has the dominant role in programmed cell death during spermatogenesis16 and in

NGF deprivation-induced killing of neuronal cells,17 whereas Bak is essential for cell death in platelets.18 To investigate whether both Bax and Bak are necessary for mast cell apoptosis we assessed cytokine deprivation-induced apoptosis in mast cells decient in bax, bak or both (bax / bak / ) and wild type. After 36 h of starvation, more

than 60% of bax / , but less than 25% of the bak / and wt CTLMC were viable. The same pattern was seen in MLMC although somewhat more rapid, with more than 60% viability of bax / mast cells and less than 25% of the bak / or wt already at 24 h (Figure 3a and b). Notably, only combined loss of both Bax and Bak conferred complete resistance to cytokine deprivation, which demonstrates that Bak does have a role in mast cell apoptosis, albeit a lesser one compared with Bax.

Discussion

In the present study we have analyzed the individual and combined roles of Bax and Bak in cytokine deprivation-induced apoptosis in two mast cell sub-populations, MLMC and CTLMC. We show that Bax has a more prominent role in mast cell apoptosis than Bak, because mast cells lacking Bax have an increased and prolonged survival compared with Bak-decient mast cells. However, only combined loss of both Bak and Bax conferred complete resistance to cytokine deprivation to a comparable extent as Bcl-2 overexpression or combined loss of Puma and Bim (Figure 3c and d and Alfredsson et al.11 and Ekoff et al.12). This shows that Bak does have a function in mast cell apoptosis induced by cytokine deprivation, albeit a lesser one compared with Bax. Both Bax and Bak proteins are expressed in mast cells,

Figure 3 (a and b) Loss of Bax protects both CTLMC and MLMC from cytokine deprivation-induced apoptosis more potently than loss of Bak. Mast cells from wt, bax / , bak / and bax / bak / mice were deprived on cytokines for 86 or 40 h, respectively. Cell viability was analyzed by PI staining and FACS analysis. Data are presented as mean (S.E.M.) of three independent experiments. (c and d) Survival of CTLMC and MLMC from wt, bim / puma / and vav-bcl-2 transgenic mice in absence of cytokines was also analyzed by PI staining and FACS analysis. Data are presented as mean (S.D.) of at least three independent experiments. (e) A schematic picture illustrating the model of indirect activation of apoptosis involving the three groups of Bcl-2 family proteins controlling cell fate: proapoptotic BH3-only proteins (Bim and Puma), anti-apoptotic Bcl-2-like proteins (Bcl-2) and effector proteins (Bax/Bak)

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however, the level of Bax is higher than Bak, which could be a plausible explanation for the increased survival in Baxdecient mast cells when compared with those lacking Bak. In addition, the augmented survival of mast cells decient in Bak may be an effect of redundancy between the two effector proteins.

MLMC and CTLMC overexpressing Bcl-2, or cells decient in the two BH3-only proteins Bim and Puma, resemble Bak/Bax double-decient mast cells in their profound resistance to cytokine deprivation-induced apoptosis. By affecting critical Bcl-2 family proteins in each of the three levels of the model of indirect activation of apoptosis (Figure 3 and Willis et al.3,

Chen et al.19 and Willis et al.20) cytokine deprivation-induced apoptosis in mast cells can be inhibited. According to this model, pro-apoptotic BH3-only proteins activate Bak and Bax only by neutralizing pro-survival proteins such as Bcl-2, and not by direct interaction between Bak/Bax and the BH3-only proteins (Figure 3e). Our previous ndings together with the data presented here indicate that the two BH3-only proteins Bim and Puma are essential for cytokine deprivation-induced apoptosis in mast cells and that Bim and Puma together interact with and neutralize all pro-survival proteins involved. Furthermore, overexpressing Bcl-2 in mast cells is sufcient for profound resistance to cytokine deprivation-induced apoptosis, suggesting that Bcl-2 keeps both effector proteins in check. In mouse embryo broblasts, Bak is restrained by the pro-survival proteins Mcl-1 and Bcl-xL, but not Bcl-2,20 whereas Bax is probably inhibited by the pro-survival proteins Bcl-2, Bcl-w, Bcl-xL and Mcl-1.3 Our data about Bax having a more prominent role compared with Bak in cytokine deprivation-induced apoptosis in mast cells might conduce to explain why mast cells overexpressing Bcl-2 are totally resistant to apoptosis.

The data presented here are in accordance with a previous report in which IL-3 derived bone marrow mast cells from bax / mice were shown to have an increased survival upon cytokine deprivation.21 They also found an increase in mast cell numbers in the stomach mucosa and a minor increase of mast cells in back skin of bax / mice compared with wild-type mice. This indicates that for mast cell homeostasis, Bax has a more prominent role in mucosal mast cells compared with connective tissue mast cells. By contrast, our in vitro data reveal no difference in the importance of Bax for the induction of apoptosis in MLMC and CTLMC, suggesting other additional mechanisms in vivo.

Mast cells are implicated in a number of different diseases where reducing their numbers would be benecial for reducing the severity of the symptoms, and in the best scenario contribute to cure the disease. These diseases include mast cell-driven diseases like mastocytosis22 and allergic reactions, but also chronic inammations such as atherosclerosis and autoimmune diseases2325 and tumors.26

In summary, in this paper we have analyzed the roles of the two pro-apoptotic proteins Bak and Bax in cytokine deprivation-induced apoptosis of CTLMC and MLMC. We report that Bax has a more prominent role than Bak in this process; however, both are needed because only bax / bak / cells were totally resistant to cytokine deprivation-induced apoptosis. Our results contribute to the work of deciphering the role of the Bcl-2 family members in the regulation of mast cell survival

and apoptosis and have implications for designing new therapeutic protocols for treatment of mast cell-associated disorders.

Materials and MethodsMice and cell cultures. The generation and genotyping of bax / , bak / , bax / bak / and bim / puma / as well as vav-bcl-2-transgenic mice have been described previously.14,16 Fetal liver-derived mast cells from wt C57BL/6 mice or mice of bax / , bak / and bax / bak / were differentiated into CTLMC or MLMC using previously described protocols.9 Briey, fetal livers from E14 mouse embryos were dissected and kept on ice in KDS BSS 10% FBS. Livers were

homogenized, cells washed in PBS and cultured at 3 105 cells per ml under

conditions promoting the development of CTLMC (RPMI-1640 supplemented with 25 ng/ml rSCF and 1 ng/ml rIL-4 (Peprotech EC Ltd, Rocky Hill, NJ, USA)) or MLMC (DMEM supplemented with 25 ng/ml rSCF, 100 U/ml IL-3 (cell supernatant from X63/0 hybridoma stably transfected with an IL-3 expression vector), 5 ng/ml rIL-9 and 1 ng/ml rTGF-b1 (both from R&D systems, Minneapolis, MN, USA)) respectively. All cells were cultured 4 weeks before being used. Similarly, bone marrow cells from wild type, vav-bcl-2-transgenic and bim / puma / were differentiated into CTLMC and MLMC using protocols described.9 All experiments with animals were performed according to the guidelines of the Royal Melbourne Hospital Research Foundation Animal Ethics Committee or the Animal Ethics Committee in Stockholm.

Detection of Kit and FceRI on mast cell surface. The cells were examined by ow cytometric analysis for expression of Kit and FceRI, using FITC-anti-mouse CD117 (Kit) mAb 2B8 or FITC-conjugated rat IgG2b isotype control (both from BD Pharmingen, San Diego, CA, USA), FITC-conjugated anti-mouse FceRI mAb MAR-1, or FITC-conjugated Armenian hamster IgG isotype control (both from eBioscience, Hateld, UK).

In vitro cell activation by IgE receptor crosslinking. CTLMCs and MLMCs were suspended at 5 105 cells per ml. For FceRI stimulation, mast cells

were sensitized for 90 min using a monoclonal murine IgE anti-TNP antibody (IgE1-b4, ATCC), supplied as a 15% hybridoma supernatant. The cells were washed twice in PBS and then challenged with 10 ng/ml TNP-BSA (coupling ratio 9, Biosearch Technologies Inc, San Francisco, CA, USA) for the time periods indicated. Cell viability was determined by propidium iodide exclusion (5 mg/ml, Sigma-Aldrich,

Steinheim, Germany) and ow cytometric analysis using a FACScan (Becton Dickinson, Franklin Lakes, NJ, USA).9

N-acetyl-b-D-hexosaminidase release assay. Cells to be used in the N-acetyl-b-D-hexosaminidase assay were resuspended in RPMI 1640 medium supplemented with 0.2% BSA (Sigma-Aldrich) before the cells were activated by IgE receptor crosslinking. For detection of the granular enzyme b-hexosaminidase, an enzymatic colorimetric assay was used as described previously.10 Briey, 60 ml of supernatant was transferred to a 96-well plate and mixed with an equal volume of substrate solution (7.5 mM p-nitrophenyl-N-acetyl-b-D-glucosaminide dissolved in 80 mM citric acid, pH 4.5). The mixture was incubated on a rocker platform for 2 h at 37 1C. After incubation, 120 ml of glycine (0.2 M, pH 10.7) was added to each well, and the absorbance at 405 and 490 nm was measured using an Emax Precision

Microplate Reader (Molecular Devices, Sunnyvale, CA, USA).

Western blot analysis. CTLMCs (1.5 106 cells) were activated by IgE

receptor cross-linking and harvested after 5 h, washed in ice-cold PBS, and lysed in RIPA buffer (50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1% NP-40, 0.5% Sodium deoxycholate, 0.1% SDS) supplemented with protease inhibitors (Roche, Mannheim, Germany). Lysates from mouse embryonic broblasts (MEF) were included as control for expression of Bax and Bak. Protein, 40 mg, was dissolved in

SDS loading buffer and size-fractionated on 12% Tris-glycine gels (Invitrogen, Carlsbad, CA, USA). Western blotting was performed using polyclonal rabbit anti-Bak antibodies (1 : 1000; Sigma-Aldrich) or a monoclonal mouse anti-Bax antibody (1 : 1000; Sigma-Aldrich), followed by horseradish peroxidase-conjugated sheep anti-rabbit IgG or sheep anti-mouse IgG antibodies (1 : 5000; Chemicon, Temecula, CA, USA). Bound antibodies were visualized by enhanced chemoluminoscence (ECL) and exposure to Hybond ECL lm (Amersham Biosciences, Uppsala, Sweden).

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RNase protection assay. Total RNA was extracted using TriPure isolation reagent (Roche). mRNA, 2 mg per sample was analyzed by RPA according to the

RiboQuant System (Becton Dickinson) protocol, using a mAPO-2 multi-probe template (Becton Dickinson). The gel was dried and exposed on Kodak lm (Eastman Kodak Company, Stockholm, Sweden) with intensifying screens at

70 1C. Quantication was performed using a phospho-imager device and MacBas V2.2 Software (Fuji Photo Film, Co. Ltd., Stockholm, Sweden).

Conict of interest

The authors declare no conict of interest.

Acknowledgements. We thank Dr. Craig Thompson for providing the bak /

mice and Dr. H Martin and P Morgan for stem cell factor. This work was supported by fellowships and grants from the Erik and Edith Fernstrms foundation for Medical Research, Karolinska Institutet, the Centre for Allergy Research at Karolinska Institutet, the Swedish Research Council-Medicine, the Swedish Cancer Foundation, Ellen, Walter and Lennart Hesselmans foundation for scientic research, Ollie and Elof Ericssons foundation, King Gustav Vs 80-years foundation (all above MK, ME, GN), UICC International Cancer Technology Transfer (No:ICR/ 04/172) (ME), Tyrolean Science Fund (TWF) (VL), National Health and Medical Research Council (Australia; program no. 257502), the Cancer Council of Victoria, the Leukemia and Lymphoma Society (New York; SCOR Grant no. 7015) and the National Cancer Institute (NIH, US; CA 80188 and CA 43540) (AS, DH).

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