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The Proapoptotic Factors Bax and Bak Regulate T Cell Proliferation through Control of Endoplasmic Reticulum Ca2+ Homeostasis
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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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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
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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
Self-citationFueling Immunity: Insights into Metabolism and Lymphocyte Function
Pearce, E. L., Poffenberger, M. C., Chang, C.-H., & Jones, R. G. (2013) · Science · doi:10.1126/science.1242454 · Cited by 1,363
Self-citationToll-like receptor–induced changes in glycolytic metabolism regulate dendritic cell activation
Krawczyk, C. M., Holowka, T., Sun, J., Blagih, J., Amiel, E., DeBerardinis, R. J., Cross, J. R., Jung, E., Thompson, C. B., Jones, R. G., et al. (2010) · Blood · doi:10.1182/blood-2009-10-249540 · Cited by 1,246
Self-citationT cell metabolism drives immunity
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Blagih, J., Coulombe, F., Vincent, E. E., Dupuy, F., Galicia-Vázquez, G., Yurchenko, E., Raissi, T. C., van der Windt, G. J. W., Viollet, B., Pearce, E. L., et al. (2015) · Immunity · doi:10.1016/j.immuni.2014.12.030 · Cited by 679
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Green, D. R., Galluzzi, L., & Kroemer, G. (2014) · Science · doi:10.1126/science.1250256 · Cited by 678
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Schenk, U., Westendorf, A. M., Radaelli, E., Casati, A., Ferro, M., Fumagalli, M., Verderio, C., Buer, J., Scanziani, E., & Grassi, F. (2008) · Science Signaling · doi:10.1126/scisignal.1160583 · Cited by 410
Raud, B., Roy, D. G., Divakaruni, A. S., Tarasenko, T. N., Franke, R., Ma, E. H., Samborska, B., Hsieh, W. Y., Wong, A., Stüve, P., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.06.002 · Cited by 401
Self-citationMa, E. H., Verway, M. J., Johnson, R. M., Roy, D. G., Steadman, M., Hayes, S., Williams, K. S., Sheldon, R. D., Samborska, B., Kosinski, P. A., et al. (2019) · Immunity · doi:10.1016/j.immuni.2019.09.003 · Cited by 379
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Vitale, I., Pietrocola, F., Guilbaud, E., Aaronson, S. A., Abrams, J., Adam, D., Agostini, M., Agostinis, P., Alnemri, E. S., Altucci, L., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01153-w · Cited by 352
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Jones, R. G., & Thompson, C. B. (2007) · Immunity · doi:10.1016/j.immuni.2007.07.008 · Cited by 349
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MacIver, N. J., Blagih, J., Saucillo, D. C., Tonelli, L., Griss, T., Rathmell, J. C., & Jones, R. G. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100367 · Cited by 235
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Kennel, K. B., & Greten, F. R. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101891 · Cited by 213
Kamiński, M. M., Sauer, S. W., Kamiński, M., Opp, S., Ruppert, T., Grigaravičius, P., Grudnik, P., Gröne, H., Krammer, P. H., & Gülow, K. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.10.009 · Cited by 208
Non-apoptotic functions of BCL-2 family proteins
Gross, A., & Katz, S. G. (2017) · Cell Death and Differentiation · doi:10.1038/cdd.2017.22 · Cited by 202
Monaco, G., Decrock, E., Akl, H., Ponsaerts, R., Vervliet, T., Luyten, T., Maeyer, M. D., Missiaen, L., Distelhorst, C., SMEDT, H. D., et al. (2011) · Cell Death and Differentiation · doi:10.1038/cdd.2011.97 · Cited by 183
Eckenrode, E. F., Yang, J., Velmurugan, G. V., Foskett, J. K., & White, C. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.096040 · Cited by 182
Self-citationYang, C., Wu, S., Mou, Z., Zhou, Q., Dai, X., Ou, Y., Chen, X., Chen, Y., Xu, C., Hu, Y., et al. (2022) · Molecular Therapy · doi:10.1016/j.ymthe.2022.01.022 · Cited by 182
Amiel, E., Everts, B., Freitas, T. C., King, I. L., Curtis, J. D., Pearce, E. L., & Pearce, E. J. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1103741 · Cited by 178
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Decuypere, J.-P., Monaco, G., Bultynck, G., Missiaen, L., SMEDT, H. D., & Parys, J. B. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.11.023 · Cited by 183
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Self-citationKwon, J., Shatynski, K. E., Chen, H., Morand, S. C., Deken, X. D., Miot, F., Leto, T. L., & Williams, M. S. (2010) · Science Signaling · doi:10.1126/scisignal.2000976 · Cited by 143
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Shanmughapriya, S., Rajan, S., Hoffman, N. E., Zhang, X., Guo, S., Kolesar, J. E., Hines, K. J., Ragheb, J. G., Jog, N. R., Caricchio, R., et al. (2015) · Science Signaling · doi:10.1126/scisignal.2005673 · Cited by 130
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Potula, R., Hawkins, B. J., Cenna, J. M., Fan, S., Dykstra, H., Ramirez, S. H., Morsey, B., Brodie, M. R., & Persidsky, Y. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903691 · Cited by 116
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Kiviluoto, S., Vervliet, T., Ivanova, H., Decuypere, J.-P., SMEDT, H. D., Missiaen, L., Bultynck, G., & Parys, J. B. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.01.026 · Cited by 109
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Self-citationZhong, J., Xu, Y., Yi, H., Su, J., Yu, H., Xiang, X., Li, X., Zhang, Z., & Sun, L. (2012) · Cancer Letters · doi:10.1016/j.canlet.2012.04.009 · Cited by 56
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Ludwinski, M. W., Sun, J., Hilliard, B. A., Gong, S., Xue, F., Carmody, R. J., DeVirgiliis, J., & Chen, Y. H. (2009) · Journal of Clinical Investigation · doi:10.1172/jci37619 · Cited by 57
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Simeoni, L., & Bogeski, I. (2015) · Biological Chemistry · doi:10.1515/hsz-2014-0312 · Cited by 52
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Danial, N. N., Giménez-Cassina, A., & Tondera, D. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-6706-0_1 · Cited by 48
Zustiak, M. P., Jose, L., Xie, Y., Zhu, J., & Betenbaugh, M. J. (2014) · Biotechnology Journal · doi:10.1002/biot.201300468 · Cited by 39
Gao, X., Luo, Z., Xiang, T., Wang, K., Li, J., & Wang, P. (2011) · Tumori Journal · doi:10.1177/030089161109700615 · Cited by 39
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Boohaker, R. J., Zhang, G., Carlson, A. L., Nemec, K. N., & Khaled, A. R. (2011) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00325.2010 · Cited by 38
Gao, X., Luo, Z., Xiang, T., Wang, K., Li, J., & Pi-long, W. (2011) · Tumori · doi:10.1700/1018.11095 · Cited by 34
Park, J., Moon, S., Lim, M., Byun, J. K., Hwang, S., Yang, S., Kim, E., Lee, H., Kim, S., Lee, J. J., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02270 · Cited by 33
Zhong, J.-X., Zhou, L., Li, Z., Wang, Y., & Gui, J. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.22 · Cited by 30
Self-citationRetractedDu, X., Tang, Y., Han, Y., Ri, S., Kim, T., Ju, K., Shi, W. M., Sun, S., Zhou, W., & Liu, G. (2020) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2020.04.030 · Cited by 26
Chen, J., Wei, H., Xie, B., Wang, B., Cheng, J., & Cheng, J. J. (2012) · Leukemia Research · doi:10.1016/j.leukres.2012.08.018 · Cited by 24
Campanella, M., Szabadkai, G., & Rizzuto, R. (2008) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.09.034 · Cited by 24
Newton, R. H., Leverrier, S., Srikanth, S., Gwack, Y., Cahalan, M. D., & Walsh, C. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000942 · Cited by 22
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García-García, E., Pino-Barrio, M. J., López-Medina, L., & Martı́nez-Serrano, A. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-06-0524 · Cited by 22
Bruserud, Ø., Selheim, F., Hernandez-Valladares, M., & Reikvam, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126356 · Cited by 23
Rundle, C. H., Wang, X., Sheng, M. H. ‐., Wergedal, J. E., Lau, K. ‐. W., & Mohan, S. (2008) · Bone · doi:10.1016/j.bone.2008.07.239 · Cited by 21
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Bassetti, M. F., White, J., Kappler, J. W., & Marrack, P. (2009) · International Immunology · doi:10.1093/intimm/dxp002 · Cited by 20
Zhang, L., Li, L., Leavesley, H. B., Zhang, X., Borowitz, J. L., & Isom, G. E. (2009) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.159103 · Cited by 20
Ni, H., Baty, C. J., Li, N., Ding, W., Gao, W., Li, M., Chen, X., Ma, J., Michalopoulos, G. K., & Yin, X. (2010) · Hepatology · doi:10.1002/hep.23672 · Cited by 20
Li, N., Lin, P., Cai, C., Pan, Z., Weisleder, N. L., & Ma, J. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00390.2008 · Cited by 18
Shi, L. Z., Saravia, J., Zeng, H., Kalupahana, N. S., Guy, C. S., Neale, G. A. M., & Chi, H. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617669114 · Cited by 19
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Zinkel, S. S., Yin, X., & Gross, A. (2012) · Oncogene · doi:10.1038/onc.2012.454 · Cited by 16
Liang, H., Wang, R., Cheng, R., Ye, Z., Zhao, N., Zhao, X., Huang, Y., Jiang, Z., Li, W., Zheng, J., et al. (2025) · Clinical and Translational Medicine · doi:10.1002/ctm2.70160 · Cited by 13
Wang, L., Yang, X., Li, D., Liang, Z., Chen, Y., Ma, G., Wang, Y., Li, Y., Liang, Y., & Niu, H. (2018) · OncoTargets and Therapy · doi:10.2147/ott.s180505 · Cited by 15
Self-citationKyriakou, S., Potamiti, L., Demosthenous, N., Amery, T., Stewart, K., Winyard, P. G., Franco, R., Pappa, A., & Panayiotidis, M. I. (2023) · Nutrients · doi:10.3390/nu15184044 · Cited by 11
IP3R function in cells of the immune system
Akimzhanov, A. M., & Boehning, D. F. (2011) · Wiley Interdisciplinary Reviews Membrane Transport and Signalling · doi:10.1002/wmts.27 · Cited by 10
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Zhang, H.-L., Liu, X.-J., Zhang, B., Peng, X., & Li, H. (2012) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2012.08.025 · Cited by 9
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Martı́nez-Serrano, A., Castillo, C. G., Courtois, E. T., García-García, E., & Liste, I. (2011) · Vitamins and hormones · doi:10.1016/b978-0-12-386015-6.00029-9 · Cited by 5
Ao, N., Dai, Y., Chen, Q., Feng, Y., Yu, J., Wang, C., Liu, F., Li, M., & Liu, G. (2019) · Technology in Cancer Research & Treatment · doi:10.1177/1533033819842546 · Cited by 4
The Origin and Evolution of Programmed Cell Death
Ameisen, J. C. (2009) · Wiley eBooks · doi:10.1002/9780470015902.a0021988 · Cited by 4
Kang, T., Usherwood, Y.-K., Reisz, J. A., Kamerkar, S. C., Culp‐Hill, R., Wilkins, O. M., Veríssimo, A. F., Kolling, F., Hung, A. M., Musial, S. C., et al. (2025) · JCI Insight · doi:10.1172/jci.insight.187680 · Cited by 4
Samia, A., Nadia, A. A. E. M., Taha, I. H., Medhat, M., & Seham, M. R. (2013) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 3
Insights into histone deacetylase inhibitors-induced cell death in cancer cell lines
Fuentes-Baile, M., García-Morales, P., Pérez-Valenciano, E., Mata‐Balaguer, T., Menéndez-Gutierrez, M. P., Romero, C. D. J., Lescure, Á. R., Martín‐Orozco, E., Mallavia, R. M., Barberá, V. M., et al. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118541 · Cited by 1
Pham, D. L., Kalluri, M., Weaver, C., Hsu, A., Gillette, A. A., Zhao, W., Kearl, T. J., Hematti, P., Shah, N. N., & Skala, M. C. (2026) · Molecular Therapy Advances · doi:10.1016/j.omta.2026.201704 · Cited by 1
Bajor, M., Kłopotowska, M., Baranowska, I., Hajduk, S., Leśniowska, N., Jurga, A., Granica, M., Łaźniewski, M., Krawczyk, M., Dziewicka, M., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-5280443/v1 · Cited by 1
Total body irradiation primes CD19-directed CAR T cells against large B-cell lymphomaPreprint
Alhomoud, M., Foley, M., Sugita, M., Fein, J. A., Yamshon, S., Martinez, L. M., Rejeski, K., Astorkia, M., Betel, D., Brentjens, R. J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.17.643462 · Cited by 1
Exploiting the Bioenergetics of Disease-Causing Lymphocytes for Selective Immunomodulation.
Wahl, D. R. (2012) · Deep Blue (University of Michigan)
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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