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The Proapoptotic Factors Bax and Bak Regulate T Cell Proliferation through Control of Endoplasmic Reticulum Ca2+ Homeostasis
Open accessAbstract
The Bcl-2-associated X protein (Bax) and Bcl-2-antagonist/killer (Bak) are essential regulators of lymphocyte apoptosis, but whether they play a role in viable T cell function remains unclear. Here, we report that T cells lacking both Bax and Bak display defects in antigen-specific proliferation because of Ca(2+)-signaling defects. Bax(-/-), Bak(-/-) T cells displayed defective T cell receptor (TCR)- and inositol-1,4,5-trisphosphate (IP(3))-dependent Ca(2+) mobilization because of altered endoplasmic reticulum (ER) Ca(2+) regulation that was reversed by Bax's reintroduction. The ability of TCR-dependent Ca(2+) signals to stimulate mitochondrial NADH production in excess of that utilized for ATP synthesis was dependent on Bax and Bak. Blunting of Ca(2+)-induced mitochondrial NADH elevation in the absence of Bax and Bak resulted in decreased reactive-oxygen-species production, which was required for T cell proliferation. Together, the data establish that Bax and Bak play an essential role in the control of T cell proliferation by modulating ER Ca(2+) release.
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“Restoring Ca2+ signals in Bax/Bak-null T cells restores mitochondrial ROS production and T cell proliferation (33).”
From Fueling Immunity: Insights into Metabolism and Lymphocyte Function (2013) · cites this paper as [33]
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“T cells lacking the apoptosis regulators Bax and Bak, which display defects in intracellular Ca2+ homeostasis, exhibit reduced Ca2+-dependent mitochondrial ROS production and T cell proliferation after TCR stimulation (33).”
From Fueling Immunity: Insights into Metabolism and Lymphocyte Function (2013) · cites this paper as [33]
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Cites
The versatility and universality of calcium signalling
Berridge, M. J., Lipp, P., & Bootman, M. D. (2000) · Nature Reviews Molecular Cell Biology · doi:10.1038/35036035 · Cited by 5,701
Self-citationProapoptotic BAX and BAK: A Requisite Gateway to Mitochondrial Dysfunction and Death
Wei, M. C., Zong, W.-X., Cheng, E. H.-Y., Lindsten, T., Panoutsakopoulou, V., Ross, A. J., Roth, K. A., MacGregor, G. R., Thompson, C. B., & Korsmeyer, S. J. (2001) · Science · doi:10.1126/science.1059108 · Cited by 3,988
Self-citationThastrup, M., Cullen, P. J., Drøbak, B. K., Hanley, M. R., & Dawson, A. P. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.7.2466 · Cited by 3,272
Cheng, E. H. Y., Wei, M. C., Weiler, S., Flavell, R. A., Mak, T. W., Lindsten, T., & Korsmeyer, S. J. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00320-3 · Cited by 1,735
Self-citationNovack, D. V., Sorenson, C. M., Shutter, J. R., & Korsmeyer, S. J. (1993) · Cell · doi:10.1016/0092-8674(93)80065-m · Cited by 1,637
Lindsten, T., Ross, A. J., King, A., Zong, W.-X., Rathmell, J. C., Shiels, H. A., Ulrich, E., Waymire, K. G., Mahar, P., Frauwirth, K., et al. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00136-2 · Cited by 1,489
Self-citationThe CD28 Signaling Pathway Regulates Glucose Metabolism
Frauwirth, K. A., Riley, J. L., Harris, M. H., Parry, R. V., Rathmell, J. C., Plas, D. R., Elstrom, R. L., June, C. H., & Thompson, C. B. (2002) · Immunity · doi:10.1016/s1074-7613(02)00323-0 · Cited by 1,475 · cited 2×
“TCR ligation activates pathways of cellular metabolism for energy production to meet the increased bioenergetic demands of cell growth and proliferation (Krauss et al., 2001; Frauwirth et al., 2002).”
BackgroundSelf-citationBAX and BAK Regulation of Endoplasmic Reticulum Ca 2+ : A Control Point for Apoptosis
Scorrano, L., Oakes, S. A., Opferman, J. T., Cheng, E. H. Y., Sorcinelli, M. D., Pozzan, T., & Korsmeyer, S. J. (2003) · Science · doi:10.1126/science.1081208 · Cited by 1,387
tBID, a membrane-targeted death ligand, oligomerizes BAK to release cytochrome cPreprint
Wei, M. C., Lindsten, T., Mootha, V. K., Weiler, S., Gross, A., Ashiya, M., Thompson, C. B., & Korsmeyer, S. J. (2000) · Genes & Development · doi:10.1101/gad.14.16.2060 · Cited by 1,292
Self-citationMitochondria and calcium: from cell signalling to cell death
Duchen, M. R. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00057.x · Cited by 1,261
Rizzuto, R., Brini, M., Murgia, M., & Pozzan, T. (1993) · Science · doi:10.1126/science.8235595 · Cited by 1,207
bcl-2 inhibits multiple forms of apoptosis but not negative selection in thymocytes
Sentman, C. L., Shutter, J. R., Hockenbery, D. M., Kanagawa, O., & Korsmeyer, S. J. (1991) · Cell · doi:10.1016/0092-8674(91)90361-2 · Cited by 1,188
Massive Cell Death of Immature Hematopoietic Cells and Neurons in Bcl-x-Deficient Mice
Motoyama, N., Wang, F., Roth, K. A., Sawa, H., Nakayama, K., Nakayama, K., Negishi, I., Senju, S., Zhang, Q., Fujii, S., et al. (1995) · Science · doi:10.1126/science.7878471 · Cited by 1,164
Decoding of cytosolic calcium oscillations in the mitochondria
Hajnóczky, G., Gaspers, L. D., Seitz, M. B., & Thomas, A. P. (1995) · Cell · doi:10.1016/0092-8674(95)90430-1 · Cited by 1,110
bcl-2 transgene inhibits T cell death and perturbs thymic self-censorship
Strasser, A., Harris, A. W., & Cory, S. (1991) · Cell · doi:10.1016/0092-8674(91)90362-3 · Cited by 1,054
Calcium signaling mechanisms in T lymphocytes.
Lewis, R. S. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.497 · Cited by 860
Bax and Bak can localize to the endoplasmic reticulum to initiate apoptosis
Zong, W., Li, C., Hatzivassiliou, G., Lindsten, T., Yu, Q., Yuan, J., & Thompson, C. B. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200302084 · Cited by 611
Self-citationEssential role for caspase 8 in T-cell homeostasis and T-cell-mediated immunityPreprint
Salmena, L., Lemmers, B., Hakem, A., Matysiak‐Zablocki, E., Murakami, K., Au, P. Y. B., Berry, D. M., Tamblyn, L., Shehabeldin, A., Migon, E., et al. (2003) · Genes & Development · doi:10.1101/gad.1063703 · Cited by 486
Discrete Generation of Superoxide and Hydrogen Peroxide by T Cell Receptor Stimulation
Devadas, S., Zaritskaya, L., Rhee, S. G., Oberley, L., & Williams, M. S. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20010659 · Cited by 458
T cells express a phagocyte-type NADPH oxidase that is activated after T cell receptor stimulation
Jackson, S. H., Devadas, S., Kwon, J., Pinto, L. A., & Williams, M. S. (2004) · Nature Immunology · doi:10.1038/ni1096 · Cited by 457
Caspase Activation Is Required for T Cell Proliferation
Kennedy, N. J., Kataoka, T., Tschopp, J., & Budd, R. C. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.190.12.1891 · Cited by 456
Oakes, S. A., Scorrano, L., Opferman, J. T., Bassik, M. C., Nishino, M., Pozzan, T., & Korsmeyer, S. J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408352102 · Cited by 441
The endoplasmic reticulum gateway to apoptosis by Bcl-XL modulation of the InsP3R
White, C., Li, C., Yang, J., Petrenko, N. B., Madesh, M., Thompson, C. B., & Foskett, J. K. (2005) · Nature Cell Biology · doi:10.1038/ncb1302 · Cited by 415
Self-citationChen, R., Valencia, I., Zhong, F., McColl, K. S., Roderick, H. L., Bootman, M. D., Berridge, M. J., Conway, S. J., Holmes, A. B., Mignery, G. A., et al. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200309146 · Cited by 403
Self-citationNakayama, K., Nakayama, K., Negishi, I., Kuida, K., Sawa, H., & Loh, D. Y. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.9.3700 · Cited by 395
Bcl-XL and Bcl-2 repress a common pathway of cell death.
Chao, D. T., Linette, G. P., Boise, L., White, L. S., Thompson, C. B., & Korsmeyer, S. J. (1995) · The Journal of Experimental Medicine · doi:10.1084/jem.182.3.821 · Cited by 395
Self-citationControl of Apoptosis in the Immune System: Bcl-2, BH3-Only Proteins and More
Marsden, V. S., & Strasser, A. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141029 · Cited by 390
Cutting Edge: CD4 and CD8 T Cells Are Intrinsically Different in Their Proliferative Responses
Foulds, K. E., Zenewicz, L. A., Shedlock, D. J., Jiang, J. K., Troy, A. E., & Shen, H. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.4.1528 · Cited by 385
Self-citationThe cellular and molecular basis of store-operated calcium entry
Venkatachalam, K., van Rossum, D. B., Patterson, R. L., Ma, H.-T., & Gill, D. L. (2002) · Nature Cell Biology · doi:10.1038/ncb1102-e263 · Cited by 370
Cross talk between cell death and cell cycle progression: BCL-2 regulates NFAT-mediated activation.
Linette, G. P., Li, Y., Roth, K. A., & Korsmeyer, S. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.18.9545 · Cited by 328
Deficiency in Bak and Bax perturbs thymic selection and lymphoid homeostasis
Rathmell, J. C., Lindsten, T., Zong, W., Cinalli, R. M., & Thompson, C. B. (2002) · Nature Immunology · doi:10.1038/ni834 · Cited by 302
Self-citationMazel, S. M., Burtrum, D. B., & Petrie, H. T. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.183.5.2219 · Cited by 275
A Role for FADD in T Cell Activation and Development
Walsh, C. M., Wen, B. G., Chinnaiyan, A. M., O’Rourke, K. M., Dixit, V. M., & Hedrick, S. Μ. (1998) · Immunity · doi:10.1016/s1074-7613(00)80549-x · Cited by 239
Shen, H., Slifka, M. K., Matloubian, M., Jensen, E. R., Ahmed, R., & Miller, J. F. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.9.3987 · Cited by 221
Self-citationGENETIC DISORDERS OF PROGRAMMED CELL DEATH IN THE IMMUNE SYSTEM
Bidère, N., Su, H. C., & Lenardo, M. J. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.24.021605.090513 · Cited by 198
Notch1 Regulates Maturation of CD4+ and CD8+ Thymocytes by Modulating TCR Signal Strength
Izon, D. J., Punt, J. A., Xu, L., Karnell, F. G., Allman, D., Myung, P. S., Boerth, N. J., Pui, J. C., Koretzky, G. A., & Pear, W. S. (2001) · Immunity · doi:10.1016/s1074-7613(01)00107-8 · Cited by 184
T-cell signalling and autoimmunity: molecular mechanisms of disease
Ohashi, P. S. (2002) · Nature reviews. Immunology · doi:10.1038/nri822 · Cited by 148
Signaling Takes a Breath – New Quantitative Perspectives on Bioenergetics and Signal Transduction
Krauss, S., Brand, M. D., & Buttgereit, F. (2001) · Immunity · doi:10.1016/s1074-7613(01)00205-9 · Cited by 147
Effect of antioxidants on primary alloantigen-induced T cell activation and proliferation
Chaudhri, G., Clark, I. A., Hunt, N. H., Cowden, W. B., & Ceredig, R. (1986) · The Journal of Immunology · doi:10.4049/jimmunol.137.8.2646 · Cited by 138 · cited 2×
“What is the importance of Ca-dependent ROS generation for T cell activation? Experiments conducted with ROS scavengers have suggested that ROS may be required for T cell proliferation (Chaudhri et al., 1986).”
Calcium fluxes in T lymphocytes.
Donnadieu, E., Bismuth, G., & Trautmann, A. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)35689-8 · Cited by 129
Madesh, M., Hawkins, B. J., Milovanova, T. N., Bhanumathy, C. D., Joseph, S. K., RamachandraRao, S. P., Sharma, K., Kurosaki, T., & Fisher, A. B. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200505022 · Cited by 111
Self-citationImaging early steps of human T cell activation by antigen-presenting cells
Donnadieu, E., Céfaï, D., Tan, Y. P., Parésys, G., Bismuth, G., & Trautmann, A. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.9.2643 · Cited by 107
Bcl-2 differentially regulates Ca2+ signals according to the strength of T cell receptor activation
Zhong, F., Davis, M. C., McColl, K. S., & Distelhorst, C. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200506189 · Cited by 102
Bcl-X L affects Ca 2+ homeostasis by altering expression of inositol 1,4,5-trisphosphate receptors
Li, C., Fox, C. J., Master, S. R., Bindokas, V. P., Chodosh, L. A., & Thompson, C. B. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152571899 · Cited by 102
Self-citationCellular FLICE-inhibitory protein is required for T cell survival and cycling
Chau, H., Wong, V., Chen, N., Huang, H.-L., Lin, W., Mirtsos, C., Elford, A. R., Bonnard, M., Wakeham, A. C., You-Ten, A. I., et al. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050118 · Cited by 81
Scholz, W. W., Isakov, N., Mally, M. I., Theofilopoulos, A. N., & Altman, A. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)68970-7 · Cited by 36
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Kim, I., Xu, W., & Reed, J. C. (2008) · Nature Reviews Drug Discovery · doi:10.1038/nrd2755 · Cited by 1,840
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Rizzuto, R., De Stefani, D., Raffaello, A., & Mammucari, C. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3412 · Cited by 1,781
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Pearce, E. L., Walsh, M. C., Cejas, P. J., Harms, G. M., Shen, H., Wang, L.-S., Jones, R. G., & Choi, Y. (2009) · Nature · doi:10.1038/nature08097 · Cited by 1,559
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Metadata
- Authors
- Jones, R. G., Bui, T., White, C., Madesh, M., Krawczyk, C. M., Lindsten, T., Hawkins, B. J., Kubek, S., Frauwirth, K. A., Wang, Y. L., Conway, S. J., Roderick, H. L., Bootman, M. D., Shen, H., Foskett, J. K., & Thompson, C. B.
- Affiliations
- University of Pennsylvania (US)
- University of Maryland, College Park (US)
- Cornell University (US)
- Babraham Institute (GB)
- Corresponding author
- Thompson, Craig B.
- ORCID
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2007-08
- Volume
- 27
- Issue
- 2
- Pages
- 268-280
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC2714273
- OpenAlex
- W2090734911
- Cited by
- 109
- References
- 46
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 3 · 2023: 3 · 2022: 2 · 2021: 3 · 2020: 3 · 2019: 5 · 2018: 5 · 2017: 1 · 2016: 2 · 2015: 5 · 2014: 7 · 2013: 12 · 2012: 11
- FWCI
- 4.06
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- Open Research Online (The Open University) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Lirias (submittedVersion, other-oa)
- Funders
- Cancer Research Institute
- National Institutes of Health
- Biotechnology and Biological Sciences Research Council (BBS/E/B/0000C116, BBS/E/B/00001116, BBS/E/B/0000H110)
- National Cancer Institute (R01CA099179)
- National Institute of General Medical Sciences (R01GM056328)
- Abramson Family Cancer Research Institute
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- Bax, Bak, Bcl-2 family proteins, T cell proliferation, endoplasmic reticulum calcium homeostasis, calcium signaling, T cell receptor signaling, inositol trisphosphate, mitochondrial NADH, reactive oxygen species, apoptosis, T cell function
- MeSH terms
- Adenosine Triphosphate, Animals, Calcium, Endoplasmic Reticulum, Energy Metabolism, Homeostasis, Mice, Mutant Strains, Mitochondria, NAD, Receptors, Antigen, T-Cell, T-Lymphocytes, Inositol 1,4,5-Trisphosphate, Apoptosis, Reactive Oxygen Species, Calcium Signaling, Cell Proliferation, bcl-2 Homologous Antagonist-Killer Protein, bcl-2-Associated X Protein, Mice
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