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Mitophagy: mechanisms, pathophysiological roles, and analysis
Open accessAbstract
Mitochondria are essential organelles that regulate cellular energy homeostasis and cell death. The removal of damaged mitochondria through autophagy, a process called mitophagy, is thus critical for maintaining proper cellular functions. Indeed, mitophagy has been recently proposed to play critical roles in terminal differentiation of red blood cells, paternal mitochondrial degradation, neurodegenerative diseases, and ischemia or drug-induced tissue injury. Removal of damaged mitochondria through autophagy requires two steps: induction of general autophagy and priming of damaged mitochondria for selective autophagic recognition. Recent progress in mitophagy studies reveals that mitochondrial priming is mediated either by the Pink1-Parkin signaling pathway or the mitophagic receptors Nix and Bnip3. In this review, we summarize our current knowledge on the mechanisms of mitophagy. We also discuss the pathophysiological roles of mitophagy and current assays used to monitor mitophagy.
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“The PINK1/Parkin) pathway is among the best characterized pathways through which mitophagy is induced in mammalian cells[28]”
From Overexpression of pink1 or parkin in indirect flight muscles promotes mitochondrial proteostasis and extends lifespan in Drosophila melanogaster (2019) · cites this paper as [28]
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Mitochondrial Autophagy Is an HIF-1-dependent Adaptive Metabolic Response to Hypoxia
Zhang, H., Bosch-Marce, M., Shimoda, L. A., Tan, Y. S., Baek, J. H., Wesley, J. B., Gonzalez, F. J., & Semenza, G. L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800102200 · Cited by 1,601
RetractedAutophagy: Renovation of Cells and Tissues
Mizushima, N., & Komatsu, M. (2011) · Cell · doi:10.1016/j.cell.2011.10.026 · Cited by 6,615
A role for mitochondria in nlrp3 inflammasome activation
Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602
Autophagy: process and functionPreprint
Mizushima, N. (2007) · Genes & Development · doi:10.1101/gad.1599207 · Cited by 4,104
Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
Narendra, D., Tanaka, A., Suen, D.-F., & Youle, R. J. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200809125 · Cited by 4,026
Autophagy regulates lipid metabolism
Singh, R., Kaushik, S., Wang, Y., Xiang, Y., Novak, I., Komatsu, M., Tanaka, K., Cuervo, A. M., & Czaja, M. J. (2009) · Nature · doi:10.1038/nature07976 · Cited by 3,975
Loss of autophagy in the central nervous system causes neurodegeneration in mice
Komatsu, M., Waguri, S., Chiba, T., Murata, S., Iwata, J.-I., Tanida, I., Ueno, T., Koike, M., Uchiyama, Y., Kominami, E., et al. (2006) · Nature · doi:10.1038/nature04723 · Cited by 3,500
Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
Twig, G., Elorza, A., Molina, A. J. A., Mohamed, H., Wikstrom, J. D., Walzer, G., Stiles, L., Haigh, S. E., Katz, S., Las, G., et al. (2008) · The EMBO Journal · doi:10.1038/sj.emboj.7601963 · Cited by 3,082
Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049
Flagged first, then by citations
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Items 201–300 of 1,001
Paech, F., Mingard, C., Grünig, D., Abegg, V. F., Bouitbir, J., & Krähenbühl, S. (2018) · Toxicology · doi:10.1016/j.tox.2018.01.005 · Cited by 71
Belli, M., Zhang, L., Liu, X., Donjacour, A. A., Ruggeri, E., Palmerini, M. G., Nottola, S. A., Macchiarelli, G., & Rinaudo, P. F. (2019) · Human Reproduction · doi:10.1093/humrep/dez011 · Cited by 70
Zhang, Q., Kuang, H., Chen, C., Yan, J., Do-Umehara, H. C., Liu, X.-Y., Dada, L. A., Ridge, K. M., Chandel, N. S., & Liu, J. (2015) · Nature Immunology · doi:10.1038/ni.3130 · Cited by 69
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Klionsky, D. J., Abdelmohsen, K., Abe, A., Abedin, J., Abeliovich, H., Acevedo‐Arozena, A., Adachi, H., Adams, C. M., Adams, P. D., Adeli, K., et al. (2016) · Kölner Universitäts PublikationsServer (Universität zu Köln) · doi:10.5167/uzh-131237 · Cited by 69
Macroautophagy and Chaperone‐Mediated Autophagy in Heart Failure: The Known and the Unknown
Ghosh, R., & Pattison, J. S. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/8602041 · Cited by 72
CSFV induced mitochondrial fission and mitophagy to inhibit apoptosis
Gou, H., Zhao, M., Xu, H., Yuan, J., He, W., Zhu, M., Ding, H., Yi, L., & Chen, J. (2017) · Oncotarget · doi:10.18632/oncotarget.17030 · Cited by 68
Phosphorylated CAV1 activates autophagy through an interaction with BECN1 under oxidative stress
Nah, J., Yoo, S., Jung, S., Jeong, E. I., Park, M., Kaang, B., & Jung, Y. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.71 · Cited by 71
A Mechanistic Review of Mitophagy and Its Role in Protection against Alcoholic Liver Disease
Williams, J. A. R., & Ding, W. (2015) · Biomolecules · doi:10.3390/biom5042619 · Cited by 68
Self-citationEpithelial-stromal crosstalk and fibrosis in eosinophilic esophagitis
Muir, A. B., Wang, J. X., & Nakagawa, H. (2018) · Journal of Gastroenterology · doi:10.1007/s00535-018-1498-3 · Cited by 67
An, Z., Yan, J., Zhang, Y., & Pei, R. (2020) · Journal of Materials Chemistry B · doi:10.1039/d0tb01380c · Cited by 67
Role of autophagy in alcohol and drug-induced liver injury
Williams, J. A. R., & Ding, W. (2019) · Food and Chemical Toxicology · doi:10.1016/j.fct.2019.111075 · Cited by 66
Self-citationPantiya, P., Thonusin, C., Chattipakorn, N., & Chattipakorn, S. C. (2020) · Mitochondrion · doi:10.1016/j.mito.2020.08.003 · Cited by 66
Targeting Mitochondrial Metabolism as a Strategy to Treat Senescence
Lee, Y. H., Park, J. Y., Lee, H., Song, E. S., Kuk, M. U., Joo, J., Oh, S., Kwon, H. W., Park, J. T., & Park, S. C. (2021) · Cells · doi:10.3390/cells10113003 · Cited by 66
Chemotherapy Resistance: Role of Mitochondrial and Autophagic Components
Bahar, E., Han, S., Kim, J., & Yoon, H. (2022) · Cancers · doi:10.3390/cancers14061462 · Cited by 67
Lipids associated with autophagy: mechanisms and therapeutic targets
Jarocki, M., Turek, K., Saczko, J., Tarek, M., & Kulbacka, J. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-02224-8 · Cited by 68
Li, G., Zhang, H., Fu, R., Hu, X., Liu, L., Li, Y.-N., Liu, Y.-X., Liu, X. B., Hu, J., Deng, Q., et al. (2018) · Oncogene · doi:10.1038/s41388-017-0064-4 · Cited by 69
ENKHBAT, T., Nishi, M., Yoshikawa, K., Higashijima, J., Tokunaga, T., Takasu, C., Kashihara, H., Ishikawa, D., Tominaga, M., & Shimada, M. (2018) · Anticancer Research · doi:10.21873/anticanres.12980 · Cited by 66
Mitochondrial dynamics in exercise physiology
Tanaka, T., Nishimura, A., Nishiyama, K., Goto, T., Numaga‐Tomita, T., & Nishida, M. (2019) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-019-02258-3 · Cited by 67
Uncoupled turnover disrupts mitochondrial quality control in diabetic retinopathy
Hombrebueno, J. R., Cairns, L., Dutton, L. R., Lyons, T. J., Brazil, D. P., Moynagh, P. N., Curtis, T. M., & Xu, H. (2019) · JCI Insight · doi:10.1172/jci.insight.129760 · Cited by 66
Targeting Pink1-Parkin-mediated mitophagy for treating liver injury
Williams, J. A. R., & Ding, W. (2015) · Pharmacological Research · doi:10.1016/j.phrs.2015.09.020 · Cited by 65
Self-citationChakraborty, J., Caicci, F., Roy, M., & Ziviani, E. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105097 · Cited by 65
Kouroumalis, E., Voumvouraki, A., Augoustaki, A., & Samonakis, D. N. (2021) · World Journal of Hepatology · doi:10.4254/wjh.v13.i1.6 · Cited by 66
Kidney Aging and Chronic Kidney Disease
Zhang, Y., Chen, Y., & Li, X. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126585 · Cited by 72
Insights on altered mitochondrial function and dynamics in the pathogenesis of neurodegeneration
McInnes, J. (2013) · Translational Neurodegeneration · doi:10.1186/2047-9158-2-12 · Cited by 65
New methods for monitoring mitochondrial biogenesis and mitophagy in vitro and in vivo
Williams, J. A. R., Zhao, K., Jin, S., & Ding, W. (2017) · Experimental Biology and Medicine · doi:10.1177/1535370216688802 · Cited by 64
Self-citationRybchyn, M. S., De Silva, W. G. M., Sequeira, V. B., McCarthy, B. Y., Dilley, A. V., Dixon, K. M., Halliday, G. M., & Mason, R. S. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2017.11.037 · Cited by 63
Janssen, B. G., Gyselaers, W., Byun, H., Roels, H. A., Cuypers, A., Baccarelli, A., & Nawrot, T. S. (2017) · Journal of Translational Medicine · doi:10.1186/s12967-016-1113-4 · Cited by 63
Emerging role of transcription factor EB in mitochondrial quality control
Wang, S., Chen, Y., Li, X., Zhang, W., Liu, Z., Wu, M., Pan, Q., & Liu, H. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110272 · Cited by 64
Zhao, N., Yan, Q.-W., Xia, J., Zhang, X., Li, B., Yin, L., & Xu, B. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03003-4 · Cited by 64
The economics of organellar gene loss and endosymbiotic gene transfer
Kelly, S. (2021) · Genome Biology · doi:10.1186/s13059-021-02567-w · Cited by 62
The economics of organellar gene loss and endosymbiotic gene transfer
Kelly, S. (2020) · doi:10.1101/2020.10.01.322487 · Cited by 62
Autophagy and Mitophagy Promotion in a Rat Model of Endometriosis
Siracusa, R., D’Amico, R., Impellizzeri, D., Cordaro, M., Peritore, A. F., Gugliandolo, E., Crupi, R., Salinaro, A. T., Raffone, E., Genovese, T., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105074 · Cited by 61
Kalyn, M., Lee, H., Curry, J., Tu, W., Ekker, M., & Mennigen, J. A. (2023) · Environmental Pollution · doi:10.1016/j.envpol.2023.121479 · Cited by 62
Lysine deacetylases and mitochondrial dynamics in neurodegeneration
Guedes-Dias, P., & Oliveira, J. M. A. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.04.005 · Cited by 63
Mitochondrial-associated metabolic disorders: foundations, pathologies and recent progress
McInnes, J. (2013) · Nutrition & Metabolism · doi:10.1186/1743-7075-10-63 · Cited by 64
Microbiota-Mitochondria Inter-Talk: A Potential Therapeutic Strategy in Obesity and Type 2 Diabetes
Vezza, T., Abad‐Jiménez, Z., Martí‐Cabrera, M., Rocha, M., & Víctor, V. M. (2020) · Antioxidants · doi:10.3390/antiox9090848 · Cited by 61
Marycz, K., Kornicka, K., Grzesiak, J., Śmieszek, A., & Szłapka‐Kosarzewska, J. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/3718468 · Cited by 61
Organelle communication: Signaling crossroads between homeostasis and disease
Bravo, R., Torrealba, N., Paredes, F., Morales, P. E., Pennanen, C., López‐Crisosto, C., Troncoso, R., Criollo, A., Chiong, M., Hill, J. A., et al. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.01.019 · Cited by 60
Jin, C., Liu, J., Chen, Y., Guan, R., Ouyang, C., Zhu, Y., Ji, L., & Chao, H. (2016) · Scientific Reports · doi:10.1038/srep22039 · Cited by 60
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients
Borgia, D., Malena, A., Spinazzi, M., Desbats, M. A., Salviati, L., Russell, A. P., Miotto, G., Tosatto, L., Pegoraro, E., Sorarú, G., et al. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx019 · Cited by 62
Bhatti, J. S., Kumar, S., Vijayan, M., Bhatti, G. K., & Reddy, P. H. (2017) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2016.12.012 · Cited by 61
Mitochondria autophagy: a potential target for cancer therapy
Qiu, Y.-H., Zhang, T., Wang, X., Wang, M., Zhao, W., Zhou, H., Zhang, C.-H., Cai, M., Chen, X., Zhao, W., et al. (2021) · Journal of drug targeting · doi:10.1080/1061186x.2020.1867992 · Cited by 59
Wilkaniec, A., Lenkiewicz, A. M., Babiec, L., Murawska, E., Jęśko, H. M., Cieślik, M., Culmsee, C., & Adamczyk, A. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.591475 · Cited by 62
Ferutinin induces osteoblast differentiation of DPSCs via induction of KLF2 and autophagy/mitophagy
Maity, J., Barthels, D., Sarkar, J., Prateeksha, P., Deb, M., Rolph, D. N., & Das, H. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04903-9 · Cited by 60
The interplay between mitochondria and autophagy and its role in the aging process
Schiavi, A., & Ventura, N. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.02.015 · Cited by 61
Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Continuum
Shahheydari, H., Ragagnin, A., Walker, A. K., Toth, R. P., Vidal, M., Jagaraj, C. J., Perri, E. R., Konopka, A., Sultana, J. M., & Atkin, J. D. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00119 · Cited by 61
Deyu, H., Cui, L., Xianglian, L., Guo, P., Lu, Q., Wang, X., & Zonghui, Y. (2018) · Toxicology Letters · doi:10.1016/j.toxlet.2018.05.041 · Cited by 60
Hui, L., Wu, H., Wang, T.-W., Yang, N., Guo, X., & JANG, X. (2018) · Clinical & Translational Oncology · doi:10.1007/s12094-018-1958-5 · Cited by 59
Mitochondria orchestrate macrophage effector functions in atherosclerosis
Dumont, A., Lee, M., Barouillet, T., Murphy, A. J., & Yvan‐Charvet, L. (2020) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100922 · Cited by 60
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Koziorowski, D., Figura, M., Milanowski, Ł., Szlufik, S., Alster, P., Madetko‐Alster, N., & Friedman, A. (2021) · Cells · doi:10.3390/cells10030656 · Cited by 59
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Vezza, T., Díaz-Pozo, P., Canet, F., de Marañón, A. M., Abad-Jiménez, Z., García-Gargallo, C., Roldan, I., Solá, E., Bañuls, C., López‐Domènech, S., et al. (2022) · The World Journal of Men s Health · doi:10.5534/wjmh.210146 · Cited by 59
Li, Q., Zhong, X., Yao, W., Yu, J., Wang, C., Li, Z., Lai, S., Qu, F., Fu, X., Huang, X., et al. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.101753 · Cited by 58
Peroxisomal protein PEX13 functions in selective autophagy
Lee, M. Y., Sumpter, R., Zou, Z., Sirasanagandla, S., Wei, Y., Mishra, P., Rosewich, H., Crane, D. I., & Levine, B. (2016) · EMBO Reports · doi:10.15252/embr.201642443 · Cited by 59
Ma, X., Qian, H., Chen, A., Ni, H., & Ding, W. (2021) · Cells · doi:10.3390/cells10092273 · Cited by 61
Self-citationIntertwined Relationship of Mitochondrial Metabolism, Gut Microbiome and Exercise Potential
Imdad, S., Lim, W., Kim, J., & Kang, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052679 · Cited by 60
Munan, S., Ali, M., Yadav, R., Mapa, K., & Samanta, A. (2022) · Analytical Chemistry · doi:10.1021/acs.analchem.2c02177 · Cited by 57
Lysosomal Cholesterol Accumulation Sensitizes To Acetaminophen Hepatotoxicity by Impairing Mitophagy
Baulies, A., Ribas, V., Núñez, S., Torres, S., Alarcón‐Vila, C., Martínez-Gili, L., Suda, J., Ybanez, M. D., Kaplowitz, N., García‐Ruiz, C., et al. (2015) · Scientific Reports · doi:10.1038/srep18017 · Cited by 57
Nitrite-Nitric Oxide Signaling and Cardioprotection
Totzeck, M., Hendgen-Cotta, U. B., & Rassaf, T. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-55330-6_18 · Cited by 57
Mitochondrial Dysfunction and Stress Responses in Alzheimer’s Disease
Weidling, I. W., & Swerdlow, R. H. (2019) · Biology · doi:10.3390/biology8020039 · Cited by 59
Microtubule-Based Mitochondrial Dynamics as a Valuable Therapeutic Target in Cancer
Vona, R., Mileo, A. M., & Matarrese, P. (2021) · Cancers · doi:10.3390/cancers13225812 · Cited by 58
Barbieri, E., Guescini, M., Calcabrini, C., Vallorani, L., Diaz, A. R., Fimognari, C., Canonico, B., Luchetti, F., Papa, S., Battistelli, M., et al. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/5152029 · Cited by 55
Heydarpour, F., Sajadimajd, S., Mirzarazi, E., Haratipour, P., Joshi, T., Farzaei, M. H., Khan, H., & Echeverría, J. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.498758 · Cited by 57
Holder, K., & Reddy, P. H. (2020) · The Neuroscientist · doi:10.1177/1073858420960443 · Cited by 55
Si, Z., Zheng, Y., & Zhao, J. (2023) · Biomolecules · doi:10.3390/biom13060901 · Cited by 61
Chen, Y., Liu, F., Pal, S., & Hu, Q. (2024) · Chemical Society Reviews · doi:10.1039/d4cs00411f · Cited by 59
Sun, J., Ling, P., & Gao, F. (2017) · Analytical Chemistry · doi:10.1021/acs.analchem.7b03154 · Cited by 55
Song, S. B., & Hwang, E. S. (2018) · Cells · doi:10.3390/cells8010011 · Cited by 57
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Kim, D., Song, J., & Jin, E. (2021) · Cells · doi:10.3390/cells10071839 · Cited by 56
C. elegans as a model organism for human mitochondrial associated disorders
Maglioni, S., & Ventura, N. (2016) · Mitochondrion · doi:10.1016/j.mito.2016.02.003 · Cited by 54
Ahluwalia, M., Kumar, M., Ahluwalia, P. K., Rahimi, S. Y., Vender, J. R., Raju, R. P., Hess, D. C., Baban, B., Vale, F. Ĺ., Dhandapani, K. M., et al. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105192 · Cited by 55
Liu, Q., Weng, J., Li, C., Feng, Y., Xie, M., Wang, X., Chang, Q., Li, M., Chung, K. F., Adcock, I. M., et al. (2023) · Particle and Fibre Toxicology · doi:10.1186/s12989-023-00534-w · Cited by 57
Tang, Y., Liu, J., & Long, J. (2014) · Journal of Diabetes Investigation · doi:10.1111/jdi.12302 · Cited by 54
Autophagy in Alcohol-Induced Multiorgan Injury: Mechanisms and Potential Therapeutic Targets
Li, Y., Wang, S., Ni, H., Huang, H., & Ding, W. (2014) · BioMed Research International · doi:10.1155/2014/498491 · Cited by 55
Self-citationInteractions Between Hepatitis C Virus and Mitochondria: Impact on Pathogenesis and Innate Immunity
Wang, T., & Weinman, S. A. (2013) · Current Pathobiology Reports · doi:10.1007/s40139-013-0024-9 · Cited by 54
Quantification of autophagy flux using LC3 ELISA
Oh, S.-H., Choi, Y.-B., Kim, J.-H., Weihl, C. C., & Ju, J.-S. (2017) · Analytical Biochemistry · doi:10.1016/j.ab.2017.05.003 · Cited by 53
Role of autophagy in environmental neurotoxicity
Pellacani, C., & Costa, L. G. (2018) · Environmental Pollution · doi:10.1016/j.envpol.2017.12.102 · Cited by 53
Kingnate, C., Charoenkwan, K., Kumfu, S., Chattipakorn, N., & Chattipakorn, S. C. (2018) · EBioMedicine · doi:10.1016/j.ebiom.2018.07.026 · Cited by 53
Benavides, G. A., Liang, Q., Dodson, M. B., Darley-Usmar, V. M., & Zhang, J. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.09.006 · Cited by 53
Kishinevsky, S., Wang, T., Rodina, A., Chung, S. Y., Xu, C., Philip, J., Taldone, T., Joshi, S., Alpaugh, M. L., Bolaender, A., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06486-6 · Cited by 53
The multifaceted roles of mitochondria at the crossroads of cell life and death in cancer
Fontana, F., & Limonta, P. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.09.024 · Cited by 53
Li, C., Liu, Q., Chang, Q., Xie, M., Weng, J., Wang, X., Li, M., Chen, J., Huang, Y., Yang, X., et al. (2023) · Respiratory Research · doi:10.1186/s12931-023-02634-9 · Cited by 51
Mitochondrial quality control in alveolar epithelial cells damaged by S. aureus pneumonia in mice
Suliman, H. B., Kraft, B. D., Bartz, R. R., Chen, L., Welty‐Wolf, K. E., & Piantadosi, C. A. (2017) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00197.2017 · Cited by 52
Nix/BNIP3L‐dependent mitophagy accounts for airway epithelial cell injury induced by cigarette smoke
Zhang, M., Shi, R., Zhang, Y., Hu, S., Zhang, Q., Yang, X., Li, Y., & Zhang, J. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28117 · Cited by 51
Methylmalonic acid in aging and disease
Tejero, J. D., Lazure, F., & Gomes, A. P. (2023) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2023.11.001 · Cited by 50
Kong, H., Jiang, C., Hu, L., Teng, P., Zhang, Y., Pan, X.-X., Sun, X., & Liu, W. (2019) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjz002 · Cited by 51
Guo, T., Liu, T., Sun, Y., Liu, X., Xiong, R., Li, H., Li, Z., Zhang, Z., Tian, Z., & Tian, Y. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1695-x · Cited by 50
cGAS/STING: novel perspectives of the classic pathway
Gao, M., He, Y., Tang, H., Chen, X., Liu, S., & Tao, Y. (2020) · Molecular Biomedicine · doi:10.1186/s43556-020-00006-z · Cited by 50
Apoptosis or autophagy, that is the question: Two ways for muscle sacrifice towards meat
Lana, A., & Zolla, L. (2015) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2015.10.001 · Cited by 51
Kwanten, W. J., Vandewynckel, Y., Martinet, W., Winter, B. Y. D., Michielsen, P. P., Hoof, V. O. V., Driessen, A. L. C., Timmermans, J., Bédossa, P., Vlierberghe, H. V., et al. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00418.2015 · Cited by 49
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Metadata
- Authors
- Ding, W.-X., & Yin, X.-M.
- Affiliations
- University of Kansas Medical Center (US)
- Indiana University School of Medicine (US)
- Venue
- bchm
- Publisher
- Walter de Gruyter GmbH
- Published
- 2012-07-01
- Volume
- 393
- Issue
- 7
- Pages
- 547-564
- ISSN
- 1431-6730 (ISSN-L)
- 1437-4315
- PMC
- PMC3630798
- OpenAlex
- W2076769172
- Cited by
- 1,032
- References
- 166
- Citations by year
- 2026: 47 · 2025: 77 · 2024: 83 · 2023: 99 · 2022: 90 · 2021: 115 · 2020: 111 · 2019: 98 · 2018: 67 · 2017: 64 · 2016: 59 · 2015: 44 · 2014: 50 · 2013: 25 · 2012: 1
- FWCI
- 4.79
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Biological Chemistry (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- IUScholarWorks (Indiana University) (submittedVersion)
- Funders
- National Institutes of Health (AA020518, RR016475)
- National Institute on Alcohol Abuse and Alcoholism (R01AA020518, R21AA017421, R37AA020518)
- National Cancer Institute (R01CA83817, R01CA083817)
- National Institute of General Medical Sciences (P20GM103418)
- National Center for Research Resources (P20RR021940, RR016475, P20RR016475)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- mitophagy, PINK1/Parkin pathway, Nix, BNIP3, mitochondrial priming, selective autophagy, neurodegenerative diseases, ischemia, energy homeostasis, cell death
- MeSH terms
- Aging, Animals, Disease, Humans, Mitochondria, Signal Transduction, Mitochondrial Proteins, Mitophagy
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