The DOI matches its Crossref record; 123 of the 123 references it cites were found in a registry or an index.
Mitochondria: More Than Just a Powerhouse
Open accessAbstract
Pioneering biochemical studies have long forged the concept that the mitochondria are the 'energy powerhouse of the cell'. These studies, combined with the unique evolutionary origin of the mitochondria, led the way to decades of research focusing on the organelle as an essential, yet independent, functional component of the cell. Recently, however, our conceptual view of this isolated organelle has been profoundly altered with the discovery that mitochondria function within an integrated reticulum that is continually remodeled by both fusion and fission events. The identification of a number of proteins that regulate these activities is beginning to provide mechanistic details of mitochondrial membrane remodeling. However, the broader question remains regarding the underlying purpose of mitochondrial dynamics and the translation of these morphological transitions into altered functional output. One hypothesis has been that mitochondrial respiration and metabolism may be spatially and temporally regulated by the architecture and positioning of the organelle. Recent evidence supports and expands this idea by demonstrating that mitochondria are an integral part of multiple cell signaling cascades. Interestingly, proteins such as GTPases, kinases and phosphatases are involved in bi-directional communication between the mitochondrial reticulum and the rest of the cell. These proteins link mitochondrial function and dynamics to the regulation of metabolism, cell-cycle control, development, antiviral responses and cell death. In this review we will highlight the emerging evidence that provides molecular definition to mitochondria as a central platform in the execution of diverse cellular events.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Normally, mitochondria use electrons from different carbon sources to generate a proton gradient across the inner mitochondrial membrane. The energy of this gradient is used to generate ATP (9, 30).”
From Mitochondrial Dysfunction Contributes to Oncogene-Induced Senescence (2009) · cites this paper as [30]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Inhibition of glycogen synthase kinase-3 by insulin mediated by protein kinase B
Cross, D. A. E., Alessi, D. R., Cohen, P., Andjelkovich, M., & Hemmings, B. A. (1995) · Nature · doi:10.1038/378785a0 · Cited by 5,244
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
Valente, E. M., Abou-Sleiman, P. M., Caputo, V., Muqit, M. M. K., Harvey, K., Gispert, S., Ali, Z., Del Turco, D., Bentivoglio, A. R., Healy, D. G., et al. (2004) · Science · doi:10.1126/science.1096284 · Cited by 3,481
Rab proteins as membrane organizers
Zerial, M., & McBride, H. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35052055 · Cited by 3,381
Self-citationSeth, R. B., Sun, L., Ea, C.-K., & Chen, Z. J. (2005) · Cell · doi:10.1016/j.cell.2005.08.012 · Cited by 3,329
Critical nodes in signalling pathways: insights into insulin action
Taniguchi, C. M., Emanuelli, B., & Kahn, C. R. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1837 · Cited by 2,760
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
IPS-1, an adaptor triggering RIG-I- and Mda5-mediated type I interferon induction
Kawai, T., Takahashi, K., Sato, S., Coban, C., Kumar, H., Kato, H., Ishii, K. J., Takeuchi, O., & Akira, S. (2005) · Nature Immunology · doi:10.1038/ni1243 · Cited by 2,562
Cardif is an adaptor protein in the RIG-I antiviral pathway and is targeted by hepatitis C virus
Meylan, E., Curran, J., Hofmann, K., Moradpour, D., Binder, M., Bartenschlager, R., & Tschopp, J. (2005) · Nature · doi:10.1038/nature04193 · Cited by 2,401
The p53 pathway: positive and negative feedback loops
Harris, S. L., & Levine, A. J. (2005) · Oncogene · doi:10.1038/sj.onc.1208615 · Cited by 1,967
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
Flagged first, then by citations
Cited by
Sorted by citations
Items 501–600 of 1,003
Wu, Y., Wu, S., & Wei, Y. (2014) · Free Radical Research · doi:10.3109/10715762.2014.920956 · Cited by 58
Metabolic control via the mitochondrial protein import machinery
Opalińska, M., & Meisinger, C. (2014) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2014.11.001 · Cited by 58
The Phosphorylation-Dependent Regulation of Mitochondrial Proteins in Stress Responses
Kanamaru, Y., Sekine, S., Ichijo, H., & Takeda, K. (2012) · Journal of Signal Transduction · doi:10.1155/2012/931215 · Cited by 62
Habitual Physical Activity in Mitochondrial Disease
Apabhai, S., Gorman, G. S., Sutton, L., Elson, J. L., Plötz, T., Turnbull, D. M., & Trenell, M. I. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022294 · Cited by 55
Jhuang, H., Lee, H., & Leu, J. (2016) · EMBO Reports · doi:10.15252/embr.201643311 · Cited by 57
“Mitochondria play essential roles in the survival, growth, and sexual reproduction of organisms [14].”
Asl, M. H., Khelejani, F. P., Mahdavi, S. Z. B., Emrahi, L., Jebelli, A., & Mokhtarzadeh, A. (2022) · Journal of Cellular Biochemistry · doi:10.1002/jcb.30221 · Cited by 58
“Mitochondria are dynamic structures in the cells that create networks through mitochondrial fission or fusion depending on energy demands.(119) Mitochondrial fission or division occurs similarly by prokaryotic binary fission, the same way most prokaryotes are divided into two cells.”
BackgroundHalabitska, I., Бабинец, Л. С., Oksenych, V., & Kamyshnyi, O. (2024) · Biomedicines · doi:10.3390/biomedicines12081630 · Cited by 57
“This process generates ROS, which can cause oxidative stress and mitochondrial dysfunction, both associated with insulin resistance in skeletal muscle, liver, fat, and pancreas [158,169].”
BackgroundWhy are essential genes essential? - The essentiality of Saccharomyces genes
Zhang, Z., & Ren, Q. (2015) · Microbial Cell · doi:10.15698/mic2015.08.218 · Cited by 60
Xu, Y., Wang, S., Chan, H. F., Liu, Y., Li, H., He, C., Li, Z., & Chen, M. (2017) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2017.01.064 · Cited by 55
Yin, C., Li, D., Guo, X., Cao, H., Chen, Y. B., Zhou, F., Ge, N. J., Liu, Y., Guo, S., Zhao, Z., et al. (2019) · Annals of Oncology · doi:10.1093/annonc/mdz105 · Cited by 55
The basic machineries for mitochondrial protein quality control
Vazquez‐Calvo, C., Suhm, T., Büttner, S., & Ott, M. (2019) · Mitochondrion · doi:10.1016/j.mito.2019.10.003 · Cited by 56
Jiang, N., Fan, J., Xu, F., Peng, X., Mu, H., Wang, J., & Xiong, X. (2015) · Angewandte Chemie · doi:10.1002/ange.201410645 · Cited by 55
Vincow, E. S., Thomas, R. E., Merrihew, G. E., Shulman, N. J., Bammler, T. K., MacDonald, J. W., MacCoss, M. J., & Pallanck, L. J. (2019) · Autophagy · doi:10.1080/15548627.2019.1586258 · Cited by 54
Koklesová, L., Samec, M., Líšková, A., Zhai, K., Büsselberg, D., Giordano, F. A., Kubatka, P., & Golubnitschaja, O. (2021) · The EPMA Journal · doi:10.1007/s13167-021-00237-2 · Cited by 54
The Red Queen in mitochondria: cyto-nuclear co-evolution, hybrid breakdown and human disease
Chou, J., & Leu, J. (2015) · Frontiers in Genetics · doi:10.3389/fgene.2015.00187 · Cited by 54
Yang, L., Zhu, X. Q., Wang, H., Zheng, L., Zhong, Z., Li, X., Zhao, J., Kou, J., Jiang, Y., Zheng, X., et al. (2015) · International Journal of Nanomedicine · doi:10.2147/ijn.s82162 · Cited by 54
Rath, E., & Haller, D. (2011) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21944 · Cited by 55
Busija, D. W., & Katakam, P. V. G. (2014) · Journal of Vascular Research · doi:10.1159/000360765 · Cited by 51
Zhao, Q., Wang, S., Li, Y., Wang, P., Li, S., Guo, Y., & Yao, R. (2013) · Molecular Medicine Reports · doi:10.3892/mmr.2013.1321 · Cited by 54
Pathway Analyses Implicate Glial Cells in Schizophrenia
Duncan, L. E., Holmans, P., Lee, P. H., O'Dushlaine, C. T., Kirby, A. W., Smoller, J. W., Öngür, D., & Cohen, B. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089441 · Cited by 56
Fan, S., Liu, B., Sun, L., Lv, X., Lin, Z., Chen, W., Chen, W., Tang, Q.-L., Wang, Y., Su, Y., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.3659 · Cited by 54
Liu, J., Sun, Y., Zhang, H., Huo, Y., Shi, Y., Shi, H., & Guo, W. (2014) · RSC Advances · doi:10.1039/c4ra10865e · Cited by 54
Dose enhancement effects to the nucleus and mitochondria from gold nanoparticles in the cytosol
McNamara, A. L., Kam, W. W.-Y., Scales, N., McMahon, S. J., Bennett, J. W., Byrne, H. L., Schuemann, J., Paganetti, H., Banati, R. B., & Kuncic, Z. (2016) · Physics in Medicine and Biology · doi:10.1088/0031-9155/61/16/5993 · Cited by 54
“In this paper, we measured the elemental composition of a whole JURKAT cell, a human T lymphocyte primarily used in cancer drug and radiation studies (e.g. Cataldi et al (2009)) as well as the isolated JURKAT cell nucleus and mitochondrion. Although data on the composition of cells exist, these are generally only for…”
InfluentialAltered mitochondrial dynamics as a consequence of Venezuelan Equine encephalitis virus infection
Keck, F., Brooks-Faulconer, T., Lark, T., Ravishankar, P., Bailey, C., Salvador-Morales, C., & Narayanan, A. (2017) · Virulence · doi:10.1080/21505594.2016.1276690 · Cited by 56
Fan, L., Zhang, W., Wang, X., Dong, W., Tong, Y., Dong, C., & Shuang, S. (2018) · The Analyst · doi:10.1039/c8an01908h · Cited by 54
Kang, Y., Anderson, A. J., Jackson, T. D., Palmer, C. S., Souza, D. P. D., Fujihara, K. M., Stait, T. L., Frazier, A. E., Clemons, N. J., Tull, D., et al. (2019) · eLife · doi:10.7554/elife.48828 · Cited by 55
“Introduction Mitochondria are fundamental cellular organelles governing many metabolic processes including fatty acid oxidation, the Krebs cycle, oxidative phosphorylation (OXPHOS), and fatty acid ß-oxidation (Kasahara and Scorrano, 2014; McBride et al., 2006).”
BackgroundDing, S.-L., Wang, J., Jiao, J.-Q., Tu, X., Wang, Q. K., Liu, F., Li, Q., Gao, J., Zhou, Q., Gu, D. C., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.440453 · Cited by 53
The nuclear genes Mtfr1 and Dufd1 regulate mitochondrial dynamic and cellular respiration
Monticone, M., Panfoli, I., Ravera, S., Puglisi, R., Jiang, M., Morello, R., Candiani, S., Tonachini, L., Biticchi, R., Fabiano, A., et al. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22279 · Cited by 55
Molecular Chaperone Disorders: Defective Hsp60 in Neurodegeneration
Bross, P., Magnoni, R., & Bie, A. S. (2013) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026611212220005 · Cited by 54
Jiang, P., Li, H., Song, F., Cai, Y. D., Wang, J., Liu, J., & Cai, W. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17060951 · Cited by 53
Ultrasound triggered drug delivery for mitochondria targeted sonodynamic therapy
Chen, M., Xu, A., He, W., Ma, W., & Shen, S. (2017) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2017.05.009 · Cited by 53
The systems biology of mitochondrial fission and fusion and implications for disease and aging
Chauhan, A., Vera, J., & Wolkenhauer, O. (2014) · Biogerontology · doi:10.1007/s10522-013-9474-z · Cited by 52
Dikalov, S., Panov, A. V., & Dikalova, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126498 · Cited by 52
“They have many functions: synthesis, cell signaling, cell growth, and cell death [6].”
BackgroundDeath receptors and mitochondria: Two prime triggers of neural apoptosis and differentiation
Solá, S., Morgado, A. L., & Rodrigues, C. M. P. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.09.021 · Cited by 52
Zhu, J., Chen, T., Guan, J., Liu, W.-B., & Liu, J. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.06.021 · Cited by 52
High-content screening of drug-induced mitochondrial impairment in hepatic cells: effects of statins
Tolosa, L., Carmona, A. L., Castell, J. V., Gómez‐Lechón, M. J., & Donato, M. T. (2014) · Archives of Toxicology · doi:10.1007/s00204-014-1334-3 · Cited by 52
Studying mitochondrial Ca2+ uptake – A revisit
Jean-Quartier, C., Bondarenko, A. I., Alam, M. R., Trenker, M., Waldeck‐Weiermair, M., Malli, R., & Graier, W. F. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2011.10.033 · Cited by 52
Genetic Influences in Traumatic Brain Injury
Laskowitz, D., & Grant, G. A. (2015) · CRC Press eBooks · doi:10.1201/b18959-14 · Cited by 54
Kim, S. Y., Kyaw, Y. Y., & Cheong, J. (2017) · World Journal of Gastroenterology · doi:10.3748/wjg.v23.i43.7657 · Cited by 52
Systematic screens for human disease genes, from yeast to human and back
Perocchi, F., Mancera, E., & Steinmetz, L. M. (2007) · Molecular BioSystems · doi:10.1039/b709494a · Cited by 54
Mitochondria in Chronic Obstructive Pulmonary Disease and Lung Cancer: Where are We Now?
Nam, H.-S., Izumchenko, E., Dasgupta, S., & Hoque, M. O. (2017) · Biomarkers in Medicine · doi:10.2217/bmm-2016-0373 · Cited by 52
Rational design of nanocarriers for mitochondria-targeted drug delivery
Huang, L., Sun, Z., Shen, Q., Huang, Z., Wang, S., Yang, N., Li, G., Wu, Q., Wang, W., Li, L., et al. (2022) · Chinese Chemical Letters · doi:10.1016/j.cclet.2022.02.047 · Cited by 51
Mitochondria as the Essence of Yang Qi in the Human Body
Luo, J., Shiwei, S., Xia, J., Wang, J., & Gu, Z. (2022) · Phenomics · doi:10.1007/s43657-022-00060-3 · Cited by 52
“In addition to energy production, mitochondria are of central importance for multiple cellular processes, such as apoptosis, β-oxidation of fatty acids, generation of cellular metabolites, reactive oxygen species (ROS) signaling, steroid synthesis, and Ca2+ homeostasis (Camello-Almaraz et al. 2006; Hamanaka and Chande…”
BackgroundThe control of mitochondrial DNA replication during development and tumorigenesis
Lee, W., & John, J. C. S. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12873 · Cited by 50
Öhman, T., Lietzén, N., Välimäki, E., Melchjorsen, J., Matikainen, S., & Nyman, T. A. (2010) · Journal of Proteome Research · doi:10.1021/pr901040u · Cited by 50
Gennequin, C., Kouassi, S., Tidahy, H. L., Cousin, R., Lamonier, J., Garçon, G., Shirali, P., Cazier, F., Aboukaı̈s, A., & Siffert, S. (2010) · Comptes Rendus Chimie · doi:10.1016/j.crci.2010.01.001 · Cited by 50
Garbuzova-Davis, S. N., Haller, E. M., Lin, R., & Borlongan, C. V. (2017) · Stem Cells · doi:10.1002/stem.2578 · Cited by 51
hNOA1 Interacts with Complex I and DAP3 and Regulates Mitochondrial Respiration and Apoptosis
Tang, T., Zheng, B., Chen, S., Murphy, A. N., Kudlicka, K., Zhou, H., & Farquhar, M. G. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m807797200 · Cited by 48
Shearman, J. R., Sangsrakru, D., Ruang‐areerate, P., Sonthirod, C., Uthaipaisanwong, P., Yoocha, T., Poopear, S., Theerawattanasuk, K., Tragoonrung, S., & Tangphatsornruang, S. (2014) · BMC Plant Biology · doi:10.1186/1471-2229-14-45 · Cited by 49
Mitochondria-cytoskeleton associations in mammalian cytokinesis
Lawrence, E. J., Boucher, É. L., & Mandato, C. A. (2016) · Cell Division · doi:10.1186/s13008-016-0015-4 · Cited by 52
Cyclometalated iridium(III) complexes as mitochondria-targeted anticancer agents
Xiong, K., Chen, Y., Ouyang, C., Guan, R., Ji, L., & Chao, H. (2016) · Biochimie · doi:10.1016/j.biochi.2016.03.013 · Cited by 49
Rahmel, T., Marko, B., Nowak, H., Bergmann, L., Thon, P., Rump, K., Kreimendahl, S., Rassow, J., Peters, J., Singer, M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-78195-4 · Cited by 49
Busija, D. W., Rutkai, I., Dutta, S., & Katakam, P. V. G. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150051 · Cited by 52
Mitochondrial dynamics in aging and disease
Bereiter-Hahn, J. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-394625-6.00004-0 · Cited by 48
Mitochondria: the gatekeepers between metabolism and immunity
Trinchese, G., Cimmino, F., Catapano, A., Cavaliere, G., & Mollica, M. P. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1334006 · Cited by 57
Deep-Red Emissive Crescent-Shaped Fluorescent Dyes: Substituent Effect on Live Cell Imaging
Liu, W., Zhou, B., Niu, G., Ge, J., Wu, J., Zhang, H., Xu, H., & Wang, P. (2015) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5b01429 · Cited by 48
The stem cell factor/Kit signalling pathway regulates mitochondrial function and energy expenditure
Huang, Z., Ruan, H., Xian, L., Chen, W., Jiang, S., Song, A., Wang, Q., Shi, P., Gu, X., & Gao, X. (2014) · Nature Communications · doi:10.1038/ncomms5282 · Cited by 48
Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in mice
Magnoni, R., Palmfeldt, J., Christensen, J., Sand, M., Maltecca, F., Corydon, T. J., West, M. J., Casari, G., & Bross, P. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2013.02.012 · Cited by 48
Cell death: Insights into the ultrastructure of mitochondria
Ulivieri, C. (2010) · Tissue and Cell · doi:10.1016/j.tice.2010.10.004 · Cited by 50
The Ras related GTPase Miro is not required for mitochondrial transport in Dictyostelium discoideum
Vlahou, G., Eliáš, M., von Kleist-Retzow, J., Wiesner, R. J., & Rivero, F. (2010) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2010.10.012 · Cited by 50
Tricarboxylic acid cycle-sustained oxidative phosphorylation in isolated myelin vesicles
Ravera, S., Bartolucci, M., Calzia, D., Aluigi, M. G., Ramoino, P., Morelli, A. M., & Panfoli, I. (2013) · Biochimie · doi:10.1016/j.biochi.2013.07.003 · Cited by 47
Luz, A. L., Godebo, T. R., Bhatt, D. P., Ilkayeva, O., Maurer, L. L., Hirschey, M. D., & Meyer, J. N. (2016) · Toxicological Sciences · doi:10.1093/toxsci/kfw093 · Cited by 49
Sensitivity of hematopoietic stem cells to mitochondrial dysfunction by SdhD gene deletion
Bejarano-García, J. A., Millán‐Uclés, Á., Rosado, I. V., Sánchez‐Abarca, L. I., Caballero‐Velázquez, T., Durán-Galván, M. J., Pérez‐Simón, J. A., & Piruat, J. I. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.411 · Cited by 54
“15,16 19 – 21 In fact, some hematological disorders, particularly myeloid neoplasias of clonal origin, are associated to mitochondrial dysfunction.”
Parameyong, A., Govitrapong, P., & Chetsawang, B. (2015) · Mitochondrion · doi:10.1016/j.mito.2015.07.004 · Cited by 48
Loussouarn, C., Pers, Y., Bony, C., Jørgensen, C., & Noël, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.623973 · Cited by 47
Liu, B., Shah, M., Zhang, G., Liu, Q., & Pang, Y. (2014) · ACS Applied Materials & Interfaces · doi:10.1021/am506698f · Cited by 47
Ye, H., Cotic, M., Kang, E. E., Fehlings, M. G., & Carlen, P. L. (2010) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/1743-0003-7-12 · Cited by 47
Transporting mitochondria in neurons
Course, M. M., & Wang, X. (2016) · F1000Research · doi:10.12688/f1000research.7864.1 · Cited by 47
Baicalein Protects against Rotenone-Induced Neurotoxicity through Induction of Autophagy
Kuang, L., Cao, X., & Lu, Z. (2017) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b17-00392 · Cited by 49
Ong, S., Lee, W. H., Shao, N., Ismail, N. I., Katwadi, K., Lim, M.-M., Kwek, X.-Y., Michel, N. A., Li, J., Newson, J. L., et al. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.01.017 · Cited by 48
“On this background, perturbations in mitochondrial function have been demonstrated to govern cell fate (Galluzzi et al., 2012; Granville and Gottlieb, 2002; McBride et al., 2006; Ong and Gustafsson, 2012; Parone et al., 2002).”
BackgroundWash-free detection and bioimaging by AIEgens
Huang, X., Zhang, R., Chen, C., Kwok, R. T. K., & Tang, B. Z. (2020) · Materials Chemistry Frontiers · doi:10.1039/d0qm00586j · Cited by 47
Miro1-mediated mitochondrial positioning supports subcellular redox status
Alshaabi, H., Shannon, N., Gravelle, R., Milczarek, S., Messier, T., & Cunniff, B. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101818 · Cited by 47
“Mitochondria are dynamic organelles that vary in size, shape and location depending on cell type, energy status and metabolic demand for mitochondrial metabolites [1].”
BackgroundThe Complete Mitochondrial Genome of the Foodborne Parasitic Pathogen Cyclospora cayetanensis
Cinar, H. N., Gopinath, G., Jarvis, K. G., & Murphy, H. R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128645 · Cited by 47
Gα12 is targeted to the mitochondria and affects mitochondrial morphology and motility
Andreeva, A. V., Kutuzov, M. A., & Voyno-Yasenetskaya, T. (2008) · The FASEB Journal · doi:10.1096/fj.07-104224 · Cited by 47
Inhibition of proteasome reveals basal mitochondrial ubiquitination
Sulkshane, P., Duek, I., Ram, J., Thakur, A., Reis, N., Ziv, T., & Glickman, M. H. (2020) · Journal of Proteomics · doi:10.1016/j.jprot.2020.103949 · Cited by 47
Gao, S., Sun, H., Jiang, H., Li, L., Hu, X., Xu, X., & Jin, W. (2015) · Oncotarget · doi:10.18632/oncotarget.6222 · Cited by 45
Mitoepigenetics and drug addiction
Sadakierska−Chudy, A., Frankowska, M., & Filip, M. (2014) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2014.06.002 · Cited by 46
Animal Mitochondria: Evolution, Function, and Disease
Tao, M., You, C., Zhao, R., Liu, S., Zhang, Z., Zhang, C., & Liu, Y. (2013) · Current Molecular Medicine · doi:10.2174/15665240113136660081 · Cited by 46
Linking mitochondrial dynamics to mitochondrial protein quality control
Haroon, S., & Vermulst, M. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.04.004 · Cited by 46
“To meet this demand, our cells contain hundreds, or even thousands of mitochondria that fuel our cells with ATP [2].”
BackgroundMitochondrial Heterogeneity: Evaluating Mitochondrial Subpopulation Dynamics in Stem Cells
Woods, D. C. (2017) · Stem Cells International · doi:10.1155/2017/7068567 · Cited by 46
“Such functions are well characterized and ubiquitous, including cell death and differentiation, intracellular Ca regulation, oxygen sensing, and ROS generation, while others are cell and tissue type-specific, such as steroid hormone biosynthesis, hormone signaling and responsiveness, thermogenesis, hemesynthesis, and…”
Backgroundde Oliveira, M. R., Brasil, F. B., & Fürstenau, C. R. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0684-2 · Cited by 46
Physical forces modulate cell differentiation and proliferation processes
Schwartz, L. H., Moreira, J. D. V., & Jolicœur, M. (2017) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13417 · Cited by 49
“Mitochondria seem to be more than just an efficient power plant for ATP turnover [71].”
BackgroundChoi, J. W., Son, S. M., Mook‐Jung, I., Moon, Y. J., Lee, J. Y., Wang, K., Kang, H., Phi, J. H., Choi, S. A., Chong, S., et al. (2017) · Journal of neurosurgery · doi:10.3171/2017.5.jns17147 · Cited by 46
Bioimaging and Biosensing of Ferrous Ion in Neurons and HepG2 Cells upon Oxidative Stress
Liu, Z., Wang, S., Li, W., & Tian, Y. (2018) · Analytical Chemistry · doi:10.1021/acs.analchem.7b04934 · Cited by 46
Resolving complexity in mitochondrial disease: Towards precision medicine
Boggan, R. M., Lim, A. Z., Taylor, R. W., McFarland, R., & Pickett, S. J. (2019) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2019.09.003 · Cited by 46
“Mitochondria are responsive to the intra-cellular environment, and have the ability to remodel in response to changes in respiratory states, through mitochondrial fission and fusion [9].”
BackgroundWang, X., Song, A., Wang, F., Chen, M., Xiao, L., Li, Q., & Liu, N. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.06.142 · Cited by 46
CED-9 and mitochondrial homeostasis inC. elegansmuscle
Tan, F. J., Husain, M., Manlandro, C. M., Koppenol-Raab, M., Fire, A. Z., & Hill, R. B. (2008) · Journal of Cell Science · doi:10.1242/jcs.032904 · Cited by 44
Xavier, J. M., Morgado, A. L., Solá, S., & Rodrigues, C. M. P. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5417 · Cited by 45
Exercise as a therapeutic tool to prevent mitochondrial degeneration in nonalcoholic steatohepatitis
Gonçalves, I. O., Oliveira, P. J., Ascensão, A. A. M. R., & Magalhães, J. (2013) · European Journal of Clinical Investigation · doi:10.1111/eci.12146 · Cited by 46
The influence of APOE and TOMM40 polymorphisms on hippocampal volume and episodic memory in old age
Ferencz, B., Laukka, E. J., Lövdén, M., Kalpouzos, G., Keller, L., Graff, C., Wahlund, L., Fratiglioni, L., & Bäckman, L. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00198 · Cited by 45
Genetic and functional association of FAM5C with myocardial infarction
Connelly, J. J., Shah, S. H., Doss, J. F., Gadson, S., Nelson, S. C., Crosslin, D. R., Hale, A. B., Lou, X., Wang, T., Haynes, C. S., et al. (2008) · BMC Medical Genetics · doi:10.1186/1471-2350-9-33 · Cited by 45
Zhang, Y., Li, R., Ying, X., Tian, W., Yao, H.-J., Men, Y., Yu, Y., Zhang, L., Ju, R.-J., Wang, X., et al. (2010) · Molecular Pharmaceutics · doi:10.1021/mp100249x · Cited by 45
Dynamic changes in mitochondrial distribution in human oocytes during meiotic maturation
Takahashi, Y., Hashimoto, S., Yamochi, T., Goto, H., Yamanaka, M., Amo, A., Matsumoto, H., Inoue, M., Ito, K., Nakaoka, Y., et al. (2016) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-016-0716-2 · Cited by 45
Mitochondria-mediated damage to dopaminergic neurons in Parkinson's disease (Review)
Liu, X., Wang, Y., Yu, X., Li, D., & Li, G. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3255 · Cited by 45
“Defects in the ETC complexes and damage to the mitochondrial membrane potential contribute to mitochondrial network disintegration, leading to increased fragmentation and cell death (137).”
Mitochondrial PIP3-binding protein FUNDC2 supports platelet survival via AKT signaling pathway
Ma, Q., Zhu, C., Zhang, W., Ta, N., Zhang, R., Liu, L., Feng, D., Cheng, H., Liu, J., & Chen, Q. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0121-8 · Cited by 45
Amiott, E. A., Cohen, M. M., Saint-Georges, Y., Weissman, A. M., & Shaw, J. M. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-07-0622 · Cited by 51
Moore, T. M., Cheng, L., Wolf, D. M., Ngo, J., Segawa, M., Zhu, X., Strumwasser, A. R., Cao, Y., Clifford, B. L., Ma, A., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34468-2 · Cited by 49
Function of small GTPase Rho3 in regulating growth, conidiation and virulence of Botrytis cinerea
An, B., Li, B., Qin, G., & Tian, S. (2015) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2015.01.007 · Cited by 44
Mitochondrial Alterations and Neuropsychiatric Disorders
Marazziti, D., Baroni, S., Picchetti, M., Landi, P., Silvestri, S., Vatteroni, E., & Dell’Osso, M. C. (2011) · Current Medicinal Chemistry · doi:10.2174/092986711797379221 · Cited by 45
van den Akker, E. B., Passtoors, W. M., Jansen, R., van Zwet, E. W., Goeman, J. J., Hulsman, M., Emilsson, V., Perola, M., Willemsen, G. A. H. M., Penninx, B. W. J. H., et al. (2013) · Aging Cell · doi:10.1111/acel.12160 · Cited by 46
Metadata
- Authors
- McBride, H. M., Neuspiel, M., & Wasiak, S.
- Affiliations
- Ottawa Heart Institute (CA)
- Corresponding author
- McBride, Heidi M.
- Venue
- Current Biology
- Publisher
- Elsevier BV
- Published
- 2006-07
- Volume
- 16
- Issue
- 14
- Pages
- R551-R560
- ISSN
- 0960-9822 (ISSN-L)
- OpenAlex
- W2084034472
- Cited by
- 1,985
- References
- 123
- Citations by year
- 2026: 48 · 2025: 95 · 2024: 129 · 2023: 126 · 2022: 127 · 2021: 132 · 2020: 130 · 2019: 102 · 2018: 97 · 2017: 125 · 2016: 126 · 2015: 115 · 2014: 100 · 2013: 116 · 2012: 92
- FWCI
- 4.22
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 2573 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Current Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- mitochondria, mitochondrial dynamics, mitochondrial fusion, mitochondrial fission, mitochondrial reticulum, mitochondrial membrane remodeling, mitochondrial respiration, mitochondrial metabolism, signal transduction, GTPase, kinases, phosphatase, cell death, cell cycle regulation, antiviral response, organelle positioning
- MeSH terms
- Cell Division, Mitochondria, Models, Biological, Neurons, Phosphoric Monoester Hydrolases, Protein Kinases, Signal Transduction, Tumor Suppressor Protein p53, NF-kappa B, Apoptosis, ras Proteins, Mitochondrial Proteins, Mitochondrial Membranes
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review