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Roles of the Mammalian Mitochondrial Fission and Fusion Mediators Fis1, Drp1, and Opa1 in Apoptosis
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During apoptosis, the mitochondrial network fragments. Using short hairpin RNAs for RNA interference, we manipulated the expression levels of the proteins hFis1, Drp1, and Opa1 that are involved in mitochondrial fission and fusion in mammalian cells, and we characterized their functions in mitochondrial morphology and apoptosis. Down-regulation of hFis1 powerfully inhibits cell death to an extent significantly greater than down-regulation of Drp1 and at a stage of apoptosis distinct from that induced by Drp1 inhibition. Cells depleted of Opa1 are extremely sensitive to exogenous apoptosis induction, and some die spontaneously by a process that requires hFis1 expression. Wild-type Opa1 may function normally as an antiapoptotic protein, keeping spontaneous apoptosis in check. However, if hFis1 is down-regulated, cells do not require Opa1 to prevent apoptosis, suggesting that Opa1 may be normally counteracting the proapoptotic action of hFis1. We also demonstrate in this study that mitochondrial fragmentation per se does not result in apoptosis. However, we provide further evidence that multiple components of the mitochondrial morphogenesis machinery can positively and negatively regulate apoptosis.
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“A decrease in mitochondrial fusion caused by reduced levels of Opa1 can also influence the progression of cell-death pathways (Lee et al., 2004; Olichon et al., 2003).”
From New insights into the role of mitochondria in aging: mitochondrial dynamics and more (2010) · cites this paper as Lee et al., 2004
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The Release of Cytochrome c from Mitochondria: A Primary Site for Bcl-2 Regulation of Apoptosis
Kluck, R. M., Bossy‐Wetzel, E., Green, D. R., & Newmeyer, D. D. (1997) · Science · doi:10.1126/science.275.5303.1132 · Cited by 4,715
Chen, H., Detmer, S. A., Ewald, A. J., Griffin, E. E., Fraser, S. E., & Chan, D. C. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211046 · Cited by 2,601
Dynamin-related Protein Drp1 Is Required for Mitochondrial Division in Mammalian Cells
Smirnova, E., Griparić, L., Shurland, D., & van der Bliek, A. M. (2001) · Molecular Biology of the Cell · doi:10.1091/mbc.12.8.2245 · Cited by 1,938
Movement of Bax from the Cytosol to Mitochondria during Apoptosis
Wolter, K. G., Hsu, Y., Smith, C. L., Nechushtan, A., Xi, X., & Youle, R. J. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.139.5.1281 · Cited by 1,809
The Role of Dynamin-Related Protein 1, a Mediator of Mitochondrial Fission, in Apoptosis
Frank, S., Gaume, B., Bergmann-Leitner, E. S., Leitner, W. W., Robert, E. G., Catez, F., Smith, C. L., & Youle, R. J. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00055-7 · Cited by 1,755
Short hairpin RNAs (shRNAs) induce sequence-specific silencing in mammalian cellsPreprint
Paddison, P. J., Caudy, A. A., Bernstein, E., Hannon, G. J., & Conklin, D. S. (2002) · Genes & Development · doi:10.1101/gad.981002 · Cited by 1,571
Delettre, C., Lenaers, G., Griffoin, J.-M., Gigarel, N., Lorenzo, C., Belenguer, P., Pelloquin, L., Grosgeorge, J., Turc-Carel, C., Perret, E., et al. (2000) · Nature Genetics · doi:10.1038/79936 · Cited by 1,446
Alexander, C., Votruba, M., Pesch, U. E. A., Thiselton, D. L., Mayer, S., Moore, A., Rodriguez, M., Kellner, U., Leo-Kottler, B., Auburger, G., et al. (2000) · Nature Genetics · doi:10.1038/79944 · Cited by 1,330
Desagher, S., Osen‐Sand, A., Nichols, A. C., Eskes, R., Montessuit, S., Lauper, S., Maundrell, K., Antonsson, B. E., & Martinou, J. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.144.5.891 · Cited by 1,260
Olichon, A., Baricault, L., Gas, N., Guillou, E., Valette, A., Belenguer, P., & Lenaers, G. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.c200677200 · Cited by 1,168
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Banerjee, R., Mukherjee, A., & Nagotu, S. (2021) · Journal of Molecular Medicine · doi:10.1007/s00109-021-02150-7 · Cited by 40
Karbowski, M., Harwig, M. C., & Roelofs, B. A. (2014) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-801415-8.00004-7 · Cited by 41
Palermo, V., Falcone, C., Calvani, M., & Mazzoni, C. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00587.x · Cited by 39
Mitochondrial Dynamics in Peripheral Neuropathies
Sajic, M. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5822 · Cited by 40
The role of PTEN-induced kinase 1 in mitochondrial dysfunction and dynamics
Craig, K. J. T., & Cookson, M. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.02.018 · Cited by 37
Xie, W., Koppula, S., Kale, M. B., Ali, L. S., Wankhede, N. L., Umare, M. D., Upaganlawar, A. B., Abdeen, A., Ebrahim, E., El‐Sherbiny, M., et al. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1469053 · Cited by 38
New therapeutics to modulate mitochondrial dynamics and mitophagy in cardiac diseases
Disatnik, M., Hwang, S., Ferreira, J. C. B., & Mochly‐Rosen, D. (2015) · Journal of Molecular Medicine · doi:10.1007/s00109-015-1256-4 · Cited by 37
Li, Y., Yu, H., Chen, C., Li, S., Zhang, Z., Xu, H., Zhu, F., Liu, J., Spencer, P. S., Dai, Z., et al. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/5408452 · Cited by 37
Not all mitochondrial DNAs are made equal and the nucleus knows it
Lechuga‐Vieco, A. V., Justo‐Méndez, R., & Enrı́quez, J. A. (2020) · IUBMB Life · doi:10.1002/iub.2434 · Cited by 38
Yu, R., Liu, T., Jin, S., Ankarcrona, M., Lendahl, U., Nistér, M., & Zhao, J. (2021) · BMC Biology · doi:10.1186/s12915-021-01161-7 · Cited by 37
Intersection between Mitochondrial Permeability Pores and Mitochondrial Fusion/Fission
Gazaryan, I. G., & Brown, A. M. (2007) · Neurochemical Research · doi:10.1007/s11064-006-9252-2 · Cited by 37
Galindo, M. F., Solesio, M. E., Atienzar‐Aroca, S., Zamora, M. J., & Jordán, J. (2012) · Parkinson s Disease · doi:10.1155/2012/131058 · Cited by 37
Wang, C.-W., Hsu, W.-H., & Tai, C. (2016) · Oncotarget · doi:10.18632/oncotarget.13829 · Cited by 36
Pendin, D., Filadi, R., & Pizzo, P. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00102 · Cited by 35
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Rastogi, A., Joshi, P. K., Contreras, E., & Gama, V. (2019) · Cell Stress · doi:10.15698/cst2019.06.189 · Cited by 36
Shang, P., Lindberg, D. M., Starski, P. A., Peyton, L., Hong, S., Choi, S. H., & Choi, D. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.561173 · Cited by 36
Dirks‐Naylor, A. J., Kouzi, S. A., Bero, J. D., Phan, D. T., Taylor, H. N., Whitt, S. D., & Mabolo, R. (2014) · Fundamental and Clinical Pharmacology · doi:10.1111/fcp.12073 · Cited by 36
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Zhang, X., Shan, P., Homer, R., Zhang, Y., Petrache, I., Mannam, P., & Lee, P. J. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.06.017 · Cited by 36
Zhu, T., Zhang, W., Luo, P., He, F., Ge, X.-Y., Zhang, Z., & Hu, C.-P. (2017) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2017.05.003 · Cited by 36
Chen, M., Chen, Y., Zhu, W., Yan, X., Jing, X., Zhang, P., Liu, P., & Li, P. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115088 · Cited by 36
Kim, J.-E., & Kang, T. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00301 · Cited by 35
Mitochondrial Ca2+ homeostasis in lysosomal storage diseases
Kiselyov, K. I., & Muallem, S. (2008) · Cell Calcium · doi:10.1016/j.ceca.2007.12.005 · Cited by 35
Fang, L., Hemion, C., Goldblum, D., Meyer, P., Orgül, S., Frank, S., Flammer, J., & Neutzner, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052637 · Cited by 35
Bahl, V., Johnson, K., Phandthong, R., Zahedi, A., Schick, S. F., & Talbot, P. (2016) · Toxicological Sciences · doi:10.1093/toxsci/kfw102 · Cited by 37
Kowluru, R. A., & Alka, K. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098076 · Cited by 35
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Dubey, S., Shrinet, J., & Sunil, S. (2019) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0007429 · Cited by 33
Zhuang, X., Sun, X., Zhou, H., Zhang, S., Zhong, X., Xu, X., Guo, Y., Xiong, Z., Liu, M., Lin, Y., et al. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111442 · Cited by 34
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Kaczmarek, K., Studencka‐Turski, M., Meinhardt, A., Wieczerzak, K., Thoms, S., Engel, W., & Grzmil, P. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-12-0993 · Cited by 33
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Gao, J., Zhao, L., Wang, J., Zhang, L., Zhou, D., Qu, J., Wang, H., Yin, M., Hong, J., & Zhao, W. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00733 · Cited by 34
Bowes, T., & Gupta, R. S. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.08.120 · Cited by 33
Wang, C.-W., Tai, C.-J., Choong, C.-Y., Lin, Y.-C., Lee, B.-H., Shi, Y.-C., & Tai, C. (2016) · Molecules · doi:10.3390/molecules21060727 · Cited by 33
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Spano, M. (2015) · Functional Neurology · doi:10.11138/fneur/2015.30.3.151 · Cited by 36
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Schäfer, A., & Reichert, A. S. (2009) · Biological Chemistry · doi:10.1515/bc.2009.086 · Cited by 32
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Stone, J. G., Casadesús, G., Rothenberg, K. G., Siedlak, S. L., Wang, X., Zhu, X., Perry, G. L., Castellani, R. J., & Smith, M. A. (2010) · Therapeutic Advances in Chronic Disease · doi:10.1177/2040622310382817 · Cited by 32
The antiapoptotic OPA1/Parl couple participates in mitochondrial adaptation to heat shock
Szklarz, L. K. S., & Scorrano, L. (2012) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.05.001 · Cited by 32
de la Escalera, L. M., Kyrou, I., Vrbíková, J., Hainer, V., Šrámková, P., Fried, M., Piya, M. K., Kumar, S., Tripathi, G., & McTernan, P. G. (2017) · BMC Medicine · doi:10.1186/s12916-017-0797-5 · Cited by 32
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Wu, S., & Zou, M. (2018) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2018.12.018 · Cited by 33
Dasgupta, A., Chen, K., Wu, D., Hoskin, V., Mewburn, J. D., Lima, P. D. A., Parlow, L. R. G., Hindmarch, C. C. T., Martin, A. Y., Sykes, E. A., et al. (2020) · The FASEB Journal · doi:10.1096/fj.201903117r · Cited by 33
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Zhang, L., Liu, G., Lv, K., Xin, J., Wang, Y., Zhao, J., Hu, W., Xiao, C., Zhu, K., Zhu, L., et al. (2021) · Advanced Science · doi:10.1002/advs.202003348 · Cited by 32
García‐Navas, R., Liceras-Boillos, P., Gómez, C., Baltanás, F. C., Calzada, N., Nuevo‐Tapioles, C., Cuezva, J. M., & Santos, E. (2021) · Oncogene · doi:10.1038/s41388-021-01886-3 · Cited by 29
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Martins, W. C., Tasca, C. I., & Cimarosti, H. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1681-3 · Cited by 32
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Gouras, P., Ivert, L., Neuringer, M., & Nagasaki, T. (2016) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-016-3342-x · Cited by 31
Chi, Q., Liu, T., Sun, Z., Tan, S., Li, S., & Li, S. (2017) · Environmental Science and Pollution Research · doi:10.1007/s11356-017-0411-6 · Cited by 32
Zhao, Y., Sun, X., & Qi, X. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.11.031 · Cited by 33
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Matos, T. M., & Souza‐Talarico, J. N. (2019) · Dementia & Neuropsychologia · doi:10.1590/1980-57642018dn13-010002 · Cited by 35
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Han, J. W., Thompson-Lowrey, A. J., Reiss, A. B., Mayorov, V., Jia, H., Biousse, V., Newman, N. J., & Brown, M. D. (2006) · Genetics in Medicine · doi:10.1097/01.gim.0000214299.61930.c0 · Cited by 32
Varuzhanyan, G., Ladinsky, M. S., Yamashita, S., Abe, M., Sakimura, K., Kanki, T., & Chan, D. C. (2021) · Development · doi:10.1242/dev.199686 · Cited by 31
Lee, W., Chiu, C.-H., Chen, J., Chen, C.-H., & Chang, H. (2016) · DNA and Cell Biology · doi:10.1089/dna.2016.3261 · Cited by 32
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Song, Y., Li, T., Liu, Z., Xu, Z., Zhang, Z., Chi, L., & Liu, Y. (2019) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2019.03.013 · Cited by 32
Effects of apoptosis on liver aging
Hu, S., Jiang, S., Zhang, J., Luo, D., Yu, B., Yang, L.-Y., Zhong, H., Yang, M.-W., Liu, L.-Y. D., Hong, F., et al. (2019) · World Journal of Clinical Cases · doi:10.12998/wjcc.v7.i6.691 · Cited by 32
Hutto, R. A., Bisbach, C. M., Abbas, F. H., Brock, D. C., Cleghorn, W. M., Parker, E. D., Bauer, B. H., Ge, W., Vinberg, F., Hurley, J. B., et al. (2019) · Cell Death and Differentiation · doi:10.1038/s41418-019-0398-2 · Cited by 31
Zhao, L., Liu, Z., Deng, X., Wang, J., Sun, L., Fan, L., & Zhang, Y. (2020) · Oncology Reports · doi:10.3892/or.2020.7879 · Cited by 33
Apoptotic signals at the endoplasmic reticulum-mitochondria interface
Giamogante, F., Poggio, E., Barazzuol, L., Covallero, A., & Calí, T. (2021) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2021.02.007 · Cited by 30
Kalogerou, M., Ioannou, S., Kolovos, P., Prokopiou, E., Potamiti, L., Kyriacou, K. C., Panayiotidis, M. I., Ioannou, M., Fella, E., Worth, E. P., et al. (2021) · Experimental Eye Research · doi:10.1016/j.exer.2021.108901 · Cited by 31
Dentoni, G., Castro‐Aldrete, L., Naia, L., & Ankarcrona, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.920228 · Cited by 32
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Haun, F., Nakamura, T., & Lipton, S. A. (2013) · Journal of Cell Death · doi:10.4137/jcd.s10847 · Cited by 34
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Knowlton, A. A., & Liu, T. (2015) · Comprehensive physiology · doi:10.1002/cphy.c150022 · Cited by 32
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Wang, S., Zhao, H., Lin, S., Lv, Y., Lin, Y. N., Liu, Y., Peng, R., & Jin, H. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1230168 · Cited by 33
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Zhang, Z.-Y., Fan, Z., Cao, Y., Jia, Z., Li, G., Zhi, X., Yu, D., & Lv, G. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.06.021 · Cited by 30
Wang, D., Wang, Q., Yan, G., Qiao, Y., Zhu, B., Liu, B., & Tang, C. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.9079 · Cited by 28
Mishra, A., Singh, S., Tiwari, V., Bano, S., & Shukla, S. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112304 · Cited by 30
Hausenloy, D. J., & Scorrano, L. (2007) · Clinical Pharmacology & Therapeutics · doi:10.1038/sj.clpt.6100352 · Cited by 30
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Kim, D., Thairu, M. W., & Hansen, A. K. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01164 · Cited by 29
Kushnareva, Y., Seong, Y., Andreyev, A. Y., Kuwana, T., Kiosses, W. B., Votruba, M., & Newmeyer, D. D. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.160 · Cited by 28
Mikheeva, I. B., Shubina, L., Matveeva, N., Pavlik, L. L., & Kitchigina, V. F. (2017) · Epilepsy Research · doi:10.1016/j.eplepsyres.2017.09.017 · Cited by 29
Báez-Jurado, E., Guio-Vega, G. P., Hidalgo‐Lanussa, O., González, J., Echeverrı́a, V., Ashraf, G. M., Sahebkar, A., & Barreto, G. E. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1442-9 · Cited by 29
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Malik, R., Mambetsariev, I., Fricke, J., Chawla, N. S., Nam, A., Pharaon, R. R., & Salgia, R. (2020) · Advances in cancer research · doi:10.1016/bs.acr.2020.04.006 · Cited by 29
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Kim, I. S., Silwal, P., & Jo, E. (2021) · Virulence · doi:10.1080/21505594.2021.1965829 · Cited by 29
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Spinazzola, A., & Zeviani, M. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-90-481-2813-6_6 · Cited by 28
Obitsu, S., Sakata, K., Teshima, R., & Kondo, K. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.188 · Cited by 29
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Chen, L., Winger, A. J., & Knowlton, A. A. (2014) · Molecular Biology Reports · doi:10.1007/s11033-014-3663-y · Cited by 31
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Wang, A.-G., Fann, M., Yu, H.-Y., & Yen, M. (2006) · Experimental Eye Research · doi:10.1016/j.exer.2006.06.004 · Cited by 29
Song, J., Lei, X., Jiao, W., Song, Y., Chen, W., Li, J., & Chen, Z. (2018) · Scientific Reports · doi:10.1038/s41598-018-26918-z · Cited by 28
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Borkar, N. A., Thompson, M. A., Bartman, C. M., Sathish, V., Prakash, Y. S., & Pabelick, C. M. (2023) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00158.2023 · Cited by 28
Abundis, E. M., Rajapurohitam, V., Haist, J. V., Gan, X. T., & Karmazyn, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041612 · Cited by 28
Moulis, M., Millet, A. M. C., Daloyau, M., Miquel, M., Ronsin, B., Wissinger, B., Pelloquin, L., & Belenguer, P. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13894 · Cited by 28
Rasmussen, M. L., & Gama, V. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2019.12.005 · Cited by 29
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Dotto, V. D., & Carelli, V. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.681326 · Cited by 28
Mitochondrial network in the heart
Li, Q., Zhou, L., Gao, G., Jiao, J.-Q., & Li, P. (2012) · Protein & Cell · doi:10.1007/s13238-012-2921-9 · Cited by 29
Tong, Z., Fan, Y., Zhang, W., Xu, J., Cheng, J., Ding, M., & Deng, H. (2009) · Cell Research · doi:10.1038/cr.2009.42 · Cited by 28
Sarin, M., Wang, Y., Zhang, F., Rothermund, K., Zhang, Y., Lu, J. L., Sims‐Lucas, S., Beer–Stolz, D., Houten, B. V., Vockley, J., et al. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.201 · Cited by 30
Histone deacetylase inhibitors induce mitochondrial elongation
Lee, J. S., Yoon, Y. G., Yoo, S. H., Jeong, N. Y., Jeong, S. H., Lee, S. Y., Jung, D., Jeong, S., & Yoo, Y. H. (2011) · Journal of Cellular Physiology · doi:10.1002/jcp.23027 · Cited by 29
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Hwang, S. J., & Kim, W. (2013) · Chonnam Medical Journal · doi:10.4068/cmj.2013.49.3.101 · Cited by 29
Mukherjee, A., Patra, U., Bhowmick, R., & Chawla‐Sarkar, M. (2018) · Cellular Microbiology · doi:10.1111/cmi.12831 · Cited by 29
Ma, J., Zhang, X., Cao, R., Sun, L., Jing, W., Zhao, J., Zhang, S., Huang, L., & Han, C. (2019) · Journal of Cancer · doi:10.7150/jca.29756 · Cited by 28
Loucks, F. A., Schroeder, E. K., Zommer, A. E., Hilger, S., Kelsey, N. A., Bouchard, R. J., Blackstone, C. D., Brewster, J. L., & Linseman, D. A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.10.081 · Cited by 27
Ophuis, R. J. A. O., Wijers, M., Bennink, M. B., van de Loo, F. A. J., Fransen, J. A. M., Wieringa, B., & Wansink, D. G. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008024 · Cited by 27
Qin, S.-L., Deng, J. V., Lou, D., Yu, W., Pei, J.-J., & Guan, Z. (2014) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2014.06.001 · Cited by 27
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Kumari, S., Mehta, S. L., Milledge, G. Z., Huang, X., Li, H., & Li, P. (2016) · International Journal of Biological Sciences · doi:10.7150/ijbs.13589 · Cited by 30
Sun, X., Yang, Y., Xie, Y., Shi, X., Huang, L., & Tan, W. (2017) · Oncotarget · doi:10.18632/oncotarget.22969 · Cited by 27
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Metadata
- Authors
- Lee, Y.-J., Jeong, S.-Y., Karbowski, M., Smith, C. L., & Youle, R. J.
- Affiliations
- National Institutes of Health (US)
- Venue
- Molecular Biology of the Cell
- Published
- 2004-11
- Volume
- 15
- Issue
- 11
- Pages
- 5001-5011
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- PMC
- PMC524759
- OpenAlex
- W1970248089
- Cited by
- 1,042
- References
- 49
- Citations by year
- 2026: 15 · 2025: 20 · 2024: 41 · 2023: 39 · 2022: 43 · 2021: 50 · 2020: 52 · 2019: 36 · 2018: 54 · 2017: 40 · 2016: 72 · 2015: 55 · 2014: 47 · 2013: 50 · 2012: 74
- FWCI
- 14.83
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular Biology of the Cell (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- AJOU Open Repository (Ajou University) (submittedVersion)
- Funders
- National Institutes of Health
- National Heart, Lung, and Blood Institute
- National Institute of Neurological Disorders and Stroke
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- apoptosis, mitochondrial fission, mitochondrial fusion, Fis1, Drp1, OPA1, mitochondrial morphology, mitochondrial fragmentation, anti-apoptotic proteins, spontaneous apoptosis, mitochondrial morphogenesis
- MeSH terms
- HeLa Cells, Humans, Immunohistochemistry, Membrane Proteins, Microtubule-Associated Proteins, Mitochondria, Poly(ADP-ribose) Polymerases, RNA, Subcellular Fractions, Time Factors, Immunoblotting, Down-Regulation, Apoptosis, Microscopy, Confocal, GTP Phosphohydrolases, Mitochondrial Proteins, Dynamins, RNA Interference
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