The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
Transcellular degradation of axonal mitochondria
Open accessAbstract
Significance: Mitochondria are organelles that perform many essential functions, including providing the energy to cells. Cells remove damaged mitochondria through a process called mitophagy. Mitophagy is considered a subset of a process called autophagy, by which damaged organelles are enwrapped and delivered to lysosomes for degradation. Implicit in the categorization of mitophagy as a subset of autophagy, which means “self-eating,” is the assumption that a cell degrades its own mitochondria. However, we show here that in a location called the optic nerve head, large numbers of mitochondria are shed from neurons to be degraded by the lysosomes of adjoining glial cells. This finding calls into question the assumption that a cell necessarily degrades its own organelles.
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
“Cells with mitochondrial defects might release the damaged mitochondria to be picked up by other cells, thereby facilitating their degradation by recipient cells279.”
From The role of mitochondria in rheumatic diseases (2022) · cites this paper as [279]
Experimental — accuracy not yet measuredIn the citing paper
“Interestingly, degradation of neuronal mitochondria can occur in a non-cell autonomous fashion, as demonstrated by the astrocytic engulfment and degradation of mitochondria excreted from retinal ganglion cells [60].”
From Autophagy and ALS: mechanistic insights and therapeutic implications (2022) · cites this paper as [60]
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
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
Computer Visualization of Three-Dimensional Image Data Using IMOD
Kremer, J. R., Mastronarde, D. N., & McIntosh, J. R. (1996) · Journal of Structural Biology · doi:10.1006/jsbi.1996.0013 · Cited by 5,530
Cui, C., Cui, J., Jin, F., Cui, Y., Li, R., Jiang, X., Tian, Y., Wang, R. C., Jiang, P., & Gao, J. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479571 · Cited by 5,214
Pankiv, S., Clausen, T. H., Lamark, T., Brech, A., Bruun, J.-A., Outzen, H., Øvervatn, A., Bjørkøy, G., & Johansen, T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702824200 · Cited by 4,578
Circulating mitochondrial DAMPs cause inflammatory responses to injury
Zhang, Q., Raoof, M., Chen, Y., Sumi, Y., Sursal, T., Junger, W., Brohi, K., Itagaki, K., & Hauser, C. J. (2010) · Nature · doi:10.1038/nature08780 · Cited by 3,812
Mitochondrial Fission, Fusion, and Stress
Youle, R. J., & van der Bliek, A. M. (2012) · Science · doi:10.1126/science.1219855 · Cited by 3,674
The pathways of mitophagy for quality control and clearance of mitochondria
Ashrafi, G., & Schwarz, T. L. (2013) · Cell Death & Differentiation · doi:10.1038/cdd.2012.81 · Cited by 1,900
Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways
Chung, W.-S., Clarke, L. E., Wang, G. X., Stafford, B. K., Sher, A., Chakraborty, C., Joung, J., Foo, L. C., Thompson, A., Chen, C., et al. (2013) · Nature · doi:10.1038/nature12776 · Cited by 1,377 · cited 1×
“Recently, astrocytes have been shown to phagocytose whole synapses elsewhere in the visual pathway (11).”
BackgroundMitochondrial DNA that escapes from autophagy causes inflammation and heart failure
Oka, T., Hikoso, S., Yamaguchi, O., Taneike, M., Takeda, T., Tamai, T., Oyabu, J., Murakawa, T., Nakayama, H., Nishida, K., et al. (2012) · Nature · doi:10.1038/nature10992 · Cited by 1,201
Transcriptional integration of mitochondrial biogenesis
Scarpulla, R. C., Vega, R. B., & Kelly, D. P. (2012) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2012.06.006 · Cited by 798
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 679
Adlimoghaddam, A., Benson, T., & Albensi, B. C. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02937-w · Cited by 36
Mehta, S. R., Pérez‐Santiago, J., Hulgan, T., Day, T. R. C., Barnholtz‐Sloan, J. S., Gittleman, H. R., Letendre, S. L., Ellis, R. J., Heaton, R. K., Patton, S. M., et al. (2017) · Journal of Neuroinflammation · doi:10.1186/s12974-017-0848-z · Cited by 35
Astrocyte polarization in glaucoma: a new opportunity
Sun, H., Guo, W., & Liu, Y. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.339470 · Cited by 39
Brain alarm by self-extracellular nucleic acids: from neuroinflammation to neurodegeneration
Kunze, R., Fischer, S., Marti, H. H., & Preissner, K. T. (2023) · Journal of Biomedical Science · doi:10.1186/s12929-023-00954-y · Cited by 37
Caicedo, A., Zambrano, K., Sanon, S., & Gavilanes, A. W. D. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.02.006 · Cited by 34
Gharib, E., Veilleux, V., Boudreau, L. H., Pichaud, N., & Robichaud, G. A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1207631 · Cited by 37
Autophagic stress activates distinct compensatory secretory pathways in neurons
Palumbos, S. D., Popolow, J., Goldsmith, J., & Holzbaur, E. L. F. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2421886122 · Cited by 36
Neuronal endosomes to lysosomes: A journey to the soma
Kulkarni, V. V., & Maday, S. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201806139 · Cited by 33
Aharoni-Simon, M., Ben‐Yaakov, K., Sharvit-Bader, M., Raz, D., Haim, Y., Ghannam, W., Porat, N., Leiba, H., Marcovich, A. L., Eisenberg‐Lerner, A., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-08747-3 · Cited by 36
Intercellular Signalling Cross-Talk: To Kill, To Heal and To Rejuvenate
Plotnikov, E. Y., Silachev, D. N., Popkov, V. A., Zorova, L. D., Pevzner, I. B., Zorov, S. D., Jankauskas, S. S., Babenko, V. A., Sukhikh, G. T., & Zorov, D. B. (2017) · Heart Lung and Circulation · doi:10.1016/j.hlc.2016.12.002 · Cited by 35
Veilleux, V., Pichaud, N., Boudreau, L. H., & Robichaud, G. A. (2023) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-23-0329 · Cited by 38
Spaulding, H. R., Kelly, E. M., Quindry, J. C., Sheffield, J. B., Hudson, M. B., & Selsby, J. T. (2017) · Acta Physiologica · doi:10.1111/apha.12944 · Cited by 33
Welcome, M. O., & Mastorakis, N. E. (2018) · NeuroMolecular Medicine · doi:10.1007/s12017-018-8503-0 · Cited by 35
Targeted OMA1 therapies for cancer
Alavi, M. V. (2019) · International Journal of Cancer · doi:10.1002/ijc.32177 · Cited by 34
la Fuente-Muñoz, C. E. D., & Arias, C. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2020-0068 · Cited by 33
Extrusion of mitochondria: Garbage clearance or cell–cell communication signals?
Lyamzaev, K. G., Zinovkin, R. A., & Chernyak, B. V. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30711 · Cited by 34
The heterogeneity of astrocytes in glaucoma
Tang, Y., Chen, Y., & Chen, D. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2022.995369 · Cited by 36
Verkhratsky, A., & Butt, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-821565-4.00008-0 · Cited by 31
Autophagy orchestrates the crosstalk between cells and organs
Piletič, K., Alsaleh, G., & Simon, A. K. (2023) · EMBO Reports · doi:10.15252/embr.202357289 · Cited by 31
Exploring Molecular Targets for Mitochondrial Therapies in Neurodegenerative Diseases
Plascencia‐Villa, G., & Perry, G. L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512486 · Cited by 33
Extracellular vesicles as carriers for mitochondria: Biological functions and clinical applications
Liao, Z., Tong, B., Ke, W., Cao, Y., Wu, X., & Lei, M. (2024) · Mitochondrion · doi:10.1016/j.mito.2024.101935 · Cited by 35
Mitophagy-associated programmed neuronal death and neuroinflammation
Zhu, Y., Zhang, J., Deng, Q., & Chen, X. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460286 · Cited by 34
Sastri, M., Darshi, M., Mackey, M. R., Ramachandra, R., Ju, S., Phan, S., Adams, S., Stein, K. R., Douglas, C. R., Kim, J., et al. (2017) · Journal of Cell Science · doi:10.1242/jcs.201400 · Cited by 32
Self-citationSandhof, C. A., Hoppe, S. O., Druffel‐Augustin, S., Gallrein, C., Kirstein, J., Voisine, C., & Nussbaum-Krammer, C. I. (2019) · Autophagy · doi:10.1080/15548627.2019.1643657 · Cited by 32
Potential mechanisms of retinal ganglion cell type‐specific vulnerability in glaucoma
Wang, A. Y., Lee, P. Y., Bui, B. V., Jobling, A. I., Greferath, U., Brandli, A. A., Dixon, M., Findlay, Q. D., Fletcher, E. L., & Vessey, K. A. (2019) · Clinical and Experimental Optometry · doi:10.1111/cxo.13031 · Cited by 31
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
Chinnery, H. R., & Keller, K. E. (2020) · BioMed Research International · doi:10.1155/2020/7246785 · Cited by 32
Extracellular Mitochondria Signals in CNS Disorders
Park, J., & Hayakawa, K. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.642853 · Cited by 33
Mitochondrial DNA differentiates Alzheimer's disease from Creutzfeldt‐Jakob disease
Podlesniy, P., Llorens, F., Golańska, E., Sikorska, B., Liberski, P. P., Zerr, I., & Trullás, R. (2016) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2015.12.011 · Cited by 31
Khan, M. M., Paez, H. G., Pitzer, C. R., & Alway, S. E. (2022) · Current Neuropharmacology · doi:10.2174/1570159x05666220908100545 · Cited by 30
Zaninello, M., & Bean, C. (2023) · Biomolecules · doi:10.3390/biom13060938 · Cited by 34
Role of astrocytes in sleep deprivation: accomplices, resisters, or bystanders?
Que, M., Li, Y., Wang, X., Zhan, G., Luo, X., & Zhou, Z. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1188306 · Cited by 35
A mitochondrial inside-out iron-calcium signal reveals drug targets for Parkinson’s disease
Bharat, V., Durairaj, A. S., Vanhauwaert, R., Li, L., Muir, C. M., Chandra, S., Kwak, C. S., Guen, Y. L., Nandakishore, P., Hsieh, C.-H., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113544 · Cited by 31
Cai, J., Chen, Y., She, Y., He, X., Feng, H., Sun, H., Yin, M., Gao, J., Sheng, C., Li, Q., et al. (2025) · Brain Pathology · doi:10.1111/bpa.13316 · Cited by 30
Tehrani, S., Davis, L., Cepurna, W. O., Delf, R. K., Lozano, D. C., Choe, T. E., Johnson, E., & Morrison, J. (2019) · Investigative Ophthalmology and Visual Science · doi:10.1167/iovs.18-25447 · Cited by 26
Culprit or Bystander: Defective Mitophagy in Alzheimer’s Disease
Xie, C., Aman, Y., Adriaanse, B. A., Cader, M. Z., Plun‐Favreau, H., Xiao, J., & Fang, E. F. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00391 · Cited by 29
Korpershoek, J. V., Rikkers, M., Wallis, F. S. A., Dijkstra, K., Raa, M. T., de Knijff, P., Saris, D. B. F., & Vonk, L. A. (2022) · Cartilage · doi:10.1177/19476035221126346 · Cited by 31
Intracellular DAMPs in Neurodegeneration and Their Role in Clinical Therapeutics
Kaur, J., Singh, H., & Naqvi, S. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03289-9 · Cited by 32
Regenerative Potential of Carbon Monoxide in Adult Neural Circuits of the Central Nervous System
Jung, E., Koh, S., Yoo, M., & Choi, Y. K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072273 · Cited by 28
Intranasal administration of mitochondria improves spatial memory in olfactory bulbectomized mice
Bobkova, N. V., Zhdanova, D., Belosludtseva, N. V., Penkov, N. V., & Mironova, G. D. (2021) · Experimental Biology and Medicine · doi:10.1177/15353702211056866 · Cited by 29
Role of mitophagy in ocular neurodegeneration
Brooks, C. D., Kodati, B., Stankowska, D. L., & Krishnamoorthy, R. R. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1299552 · Cited by 31
Mitochondrial donation in translational medicine; from imagination to reality
Bagheri, H. S., Bani, F., Taşoğlu, S., Zarebkohan, A., Rahbarghazi, R., & Sokullu, E. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02529-z · Cited by 28
Miro proteins connect mitochondrial function and intercellular transport
Nahácka, Z., Zobalová, R., Dubisova, M., Rohlena, J., & Neužil, J. (2021) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2021.1925216 · Cited by 30
Belmares, R., Raychaudhuri, U., Maansson, S., & Clark, A. F. (2018) · Clinical Anatomy · doi:10.1002/ca.23263 · Cited by 28
Tomasello, D. L., Barrasa, M. I., Mankus, D. V., Alarcon, K. I., Lytton‐Jean, A. K. R., Liu, X. S., & Jaenisch, R. (2024) · Scientific Reports · doi:10.1038/s41598-024-71040-y · Cited by 30
Li, L., & Stary, C. M. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/6032306 · Cited by 27
Arnold, M. L., Cooper, J. F., Grant, B. D., & Driscoll, M. (2020) · Journal of Visualized Experiments · doi:10.3791/61368 · Cited by 22
Autophagy and Redox Homeostasis in Parkinson’s: A Crucial Balancing Act
Jiménez-Moreno, N., & Lane, J. D. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/8865611 · Cited by 26
The Multiple Roles of Trogocytosis in Immunity, the Nervous System, and Development
Uribe‐Querol, E., & Rosales, C. (2021) · BioMed Research International · doi:10.1155/2021/1601565 · Cited by 29
Glucose and Oxygen Metabolism after Penetrating Ballistic-Like Brain Injury
Gajavelli, S., Shimoda, K., Diaz, J. C., Yokobori, S., Spurlock, M. S., Diaz, D., Jackson, C. W., Wick, A., Zhao, W., Leung, L. Y., et al. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.243 · Cited by 26
Mitochondrial transfer from mesenchymal stem cells: Mechanisms and functions
Liu, Q., Zhang, X., Zhu, T., Xu, Z., Dong, Y., & Chen, B. (2024) · Mitochondrion · doi:10.1016/j.mito.2024.101950 · Cited by 26
Guo, Y., Fu, T., Cheng, Y., Li, Y., Zhang, R.-C., Ma, Q.-T., Wang, G., Ning, W., Fan, W., Yang, J., et al. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02287-9 · Cited by 28
A connectomics approach to understanding a retinal disease
Zucker, C. L., Bernstein, P. S., Schalek, R. L., Lichtman, J. W., & Dowling, J. E. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2011532117 · Cited by 25
Garcia, J. F., Rogers, A. V., Mak, J., Halayko, A. J., Hui, C., Xu, B., Chung, K. F., Rodríguez, T. A., Michaeloudes, C., & Bhavsar, P. K. (2022) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2022-0041oc · Cited by 27
Berridge, M. V., Crasso, C., & Neužil, J. (2015) · Molecular & Cellular Oncology · doi:10.1080/23723556.2015.1023929 · Cited by 25
Long, D. M., & Giebultowicz, J. M. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2017.01131 · Cited by 26
Astrocytes in stroke-induced neurodegeneration: a timeline
Collyer, E., & Blanco‐Suárez, E. (2023) · Frontiers in Molecular Medicine · doi:10.3389/fmmed.2023.1240862 · Cited by 26
Mitochondrial transport in neurons and evidence for its involvement in acute neurological disorders
Lu, D., Feng, Y., Liu, G., Yang, Y., Ren, Y., Chen, Z., Sun, X., Guan, Y.-X., & Wang, Z. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1268883 · Cited by 29
Targeting Mitophagy in Alzheimer’s Disease
Jayatunga, D. P. W., Hone, E., Bharadwaj, P., Garg, M. L., Verdile, G., Guillemin, G. J., & Martins, R. N. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-191258 · Cited by 25
Park, J., Lo, E. H., & Hayakawa, K. (2021) · Translational Stroke Research · doi:10.1007/s12975-021-00892-7 · Cited by 24
Local Accumulation of Axonal Mitochondria in the Optic Nerve Glial Lamina Precedes Myelination
Wilkison, S. J., Bright, C. L., Vancini, R. G., Song, D. J., Bomze, H. M., & Cartoni, R. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.678501 · Cited by 26
Highly-purified rapidly expanding clones, RECs, are superior for functional-mitochondrial transfer
Yang, J., Liu, L., Oda, Y., Wada, K., Ago, M., Matsuda, S., Hattori, M., Goto, T., Kawashima, Y., Matsuzaki, Y., et al. (2023) · Stem Cell Research & Therapy · doi:10.1186/s13287-023-03274-y · Cited by 26
Mitochondrial DNA Haplotypes as Genetic Modifiers of Cancer
Tasdogan, A., McFadden, D. G., & Mishra, P. (2020) · Trends in cancer · doi:10.1016/j.trecan.2020.08.004 · Cited by 23
The Beneficial Effect of Mitochondrial Transfer Therapy in 5XFAD Mice via Liver–Serum–Brain Response
Sweetat, S., Nitzan, K., Suissa, N., Haimovich, Y., Lichtenstein, M., Zabit, S., Benhamron, S., Akarieh, K., Mishra, K., Barasch, D., et al. (2023) · Cells · doi:10.3390/cells12071006 · Cited by 23
Astrocytes in the Optic Nerve Are Heterogeneous in Their Reactivity to Glaucomatous Injury
Zhu, Y., Wang, R., Pappas, A. C., Seifert, P. A., Savol, A. J., Sadreyev, R. I., Sun, D., & Jakobs, T. (2023) · Cells · doi:10.3390/cells12172131 · Cited by 23
Characterization of Nef expression in different brain regions of SIV-infected macaques
Yarandi, S. S., Robinson, J. A., Vakili, S., Donadoni, M., Burdo, T. H., & Sariyer, I. K. (2020) · PLoS ONE · doi:10.1371/journal.pone.0241667 · Cited by 23
Metabolic reprogramming: a new option for the treatment of spinal cord injury
Chen, J., Chen, J., Yu, C., Xia, K., Yang, B., Wang, R., Li, Y., Shi, K., Zhang, Y., Xu, H., et al. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01604 · Cited by 25
Mitochondrial dysfunction and Alzheimer’s disease: pathogenesis of mitochondrial transfer
Wei, Y., Du, X., Guo, H., Han, J., & Liu, M. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1517965 · Cited by 23
DNA repair pathways in the mitochondria
King, D. E., & Copeland, W. C. (2025) · DNA repair · doi:10.1016/j.dnarep.2025.103814 · Cited by 22
Progranulin deficiency in the brain: the interplay between neuronal and non-neuronal cells
Gawęda-Walerych, K., Aragona, V., Lodato, S., Sitek, E. J., Narożańska, E., & Buratti, E. (2025) · Translational Neurodegeneration · doi:10.1186/s40035-025-00475-8 · Cited by 22
From Cell Entry to Engraftment of Exogenous Mitochondria
Kami, D., & Gojo, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144995 · Cited by 24
Wei, W., Wu, D., Duan, Y., Elkin, K. B., Chandra, A., Guan, L., Peng, C., He, X., Wu, C., Ji, X., et al. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146406 · Cited by 22
Molecular Motors in Blood–Brain Barrier Maintenance by Astrocytes
Sobral, A. F., Costa, I. D., Teixeira, V., Silva, R. V. D. S., & Barbosa, D. J. (2025) · Brain Sciences · doi:10.3390/brainsci15030279 · Cited by 25
Liao, Y., Octaviani, S., Tian, Z., Wang, S. R., Huang, C., & Huang, J. Y. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04304-7 · Cited by 25
The context-dependent effect of cellular senescence: From embryogenesis and wound healing to aging
Lavarti, R., Alvarez-Diaz, T., Marti, K., Kar, P., & Raju, R. P. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102760 · Cited by 21
Wang, M., Wang, W., Chopp, M., Zhang, Z. G., & Zhang, Y. (2025) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x251338971 · Cited by 26
Johnson, E. C., Cepurna, W. O., Choi, D., Choe, T. E., & Morrison, J. C. (2014) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.14-15094 · Cited by 21
Wan, C., Stowell, M. H. B., & Shen, J. (2022) · Communications Biology · doi:10.1038/s42003-022-04050-z · Cited by 22
Mitochondrial Adaptations in the Growing Heart
Sánchez-Díaz, M., Nicolás-Ávila, J. Á., Cordero, M. D., & Hidalgo, A. (2020) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2020.01.006 · Cited by 21
Prieto‐Villalobos, J., Alvear, T. F., Liberona, A., Lucero, C. M. J., Martínez-Araya, C. J., Balmazabal, J., Inostroza, C. A., Ramírez, G., Gómez, G. I., & Orellana, J. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179503 · Cited by 21
Role of mitophagy in the hallmarks of aging
Wen, J., Pan, T., Li, H., Fan, H., Liu, J., Cai, Z., & Zhao, B. (2022) · Journal of Biomedical Research · doi:10.7555/jbr.36.20220045 · Cited by 20
The Role of Mitochondrial Biogenesis in Ischemic Stroke
Shademan, B., Avcı, Ç. B., Karamad, V., Soureh, G. J., Olia, J. B. H., Esmaily, F., Nourazarian, A., & Nikanfar, M. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2204088 · Cited by 22
Extracellular release in the quality control of the mammalian mitochondria
Pan, K.-H., Chang, H., & Yang, W. (2023) · Journal of Biomedical Science · doi:10.1186/s12929-023-00979-3 · Cited by 21
Huang, C.-C., Chiu, H., Lee, P., Fang, S., Lin, M., Chen, H., & Lee, J. (2023) · Molecular Pain · doi:10.1177/17448069231210423 · Cited by 20
Transfer and fates of damaged mitochondria: role in health and disease
Li, H., Sun, W., Gong, W., & Han, Y. (2024) · FEBS Journal · doi:10.1111/febs.17119 · Cited by 22
Das, A., Bell, C. M., Berlinicke, C. A., Marsh‐Armstrong, N., & Zack, D. J. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101465 · Cited by 18
Self-citationLiu, T., Wang, L., Chen, G., Tong, L., Ye, X., Yang, H. M., Liu, H., Zhang, H., Lu, W., Zhang, S., et al. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106173 · Cited by 20
Javadpour, P., Abbaszadeh, F., Ahmadiani, A., Rezaei, M., & Ghasemi, R. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04009-7 · Cited by 21
Jasutkar, H. G., Wasserlein, E. M., Ishola, A. O., Litt, N. A., Staniszewski, A., Arancio, O., & Yamamoto, A. (2024) · Autophagy · doi:10.1080/15548627.2024.2368335 · Cited by 20
Mitochondrion-based organellar therapies for central nervous system diseases
Zhao, M., Wang, J., Zhu, S., Wang, M., Chen, C., Wang, L., & Liu, J. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01843-z · Cited by 21
Trends in Mitochondrial Therapeutics for Neurological Disease
Leitão-Rocha, A., Guedes-Dias, P., Pinho, B. R., & Oliveira, J. M. A. (2015) · Current Medicinal Chemistry · doi:10.2174/0929867322666150209160317 · Cited by 19
A broad perspective on the molecular regulation of retinal ganglion cell degeneration in glaucoma
Tezel, G. (2020) · Progress in brain research · doi:10.1016/bs.pbr.2020.05.027 · Cited by 19
Astrocytes eyeball axonal mitochondria
Burdett, T. C., & Freeman, M. R. (2014) · Science · doi:10.1126/science.1258295 · Cited by 19
Regulation of mitochondrial network homeostasis by O-GlcNAcylation
Xue, Q., Yan, R., Ji, S., & Yu, S. (2022) · Mitochondrion · doi:10.1016/j.mito.2022.04.007 · Cited by 19
Mitochondria: how eminent in ageing and neurodegenerative disorders?
Bamshad, C., Najafi-Ghalehlou, N., Pourmohammadi-Bejarpasi, Z., Tomita, K., Kuwahara, Y., Sato, T., Feizkhah, A., Roushnadeh, A. M., & Roudkenar, M. H. (2022) · Human Cell · doi:10.1007/s13577-022-00833-y · Cited by 20
Verkhratsky, A., & Semyanov, A. V. (2023) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-031-26576-1_11 · Cited by 20
Mazumder, A. G., Julé, A. M., & Sun, D. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00658-9 · Cited by 20
Astrocyte Mitochondria Are a Sensitive Target of PCB52 and its Human-Relevant Metabolites
Paranjape, N., Strack, S., Lehmler, H., & Doorn, J. A. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00116 · Cited by 17
Autophagy in the mammalian nervous system: a primer for neuroscientists
Suomi, F., & McWilliams, T. G. (2019) · Neuronal Signaling · doi:10.1042/ns20180134 · Cited by 18
Molecular Basis of Neuronal Autophagy in Ageing: Insights from Caenorhabditis elegans
Konstantinidis, G., & Tavernarakis, N. (2021) · Cells · doi:10.3390/cells10030694 · Cited by 19
Metadata
- Authors
- Davis, C.-H. O., Kim, K.-Y., Bushong, E. A., Mills, E. A., Boassa, D., Shih, T., Kinebuchi, M., Phan, S., Zhou, Y., Bihlmeyer, N. A., Nguyen, J. V., Jin, Y., Ellisman, M. H., & Marsh-Armstrong, N.
- Affiliations
- Kennedy Krieger Institute (US)
- University of California San Diego (US)
- National Center for Microscopy and Imaging Research, Center for Research in Biological Systems, Department of Neurosciences, University of California at San Diego, La Jolla, CA 92093
- Johns Hopkins University (US)
- The Solomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205;
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2014-06-16
- Volume
- 111
- Issue
- 26
- Pages
- 9633-9638
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC4084443
- OpenAlex
- W2025060864
- Cited by
- 673
- References
- 29
- Citations by year
- 2026: 48 · 2025: 72 · 2024: 66 · 2023: 84 · 2022: 65 · 2021: 72 · 2020: 61 · 2019: 48 · 2018: 38 · 2017: 52 · 2016: 30 · 2015: 28 · 2014: 8
- FWCI
- 29.80
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Science Foundation (DGE-1,232,825, 1232825)
- Glaucoma Research Foundation
- Barr Foundation
- National Institutes of Health (5r01ey022680-02)
- National Institute on Drug Abuse (R01DA016602, DA016602)
- National Eye Institute (R01 EY022680, R01EY019960)
- National Institute of General Medical Sciences (R01GM082949, P41GM103412, T32GM007814, 5-T32-GM07814, 5R01GM82949)
- National Institute of Neurological Disorders and Stroke (P30NS050274)
- National Center for Research Resources (P41RR004050, DA016602)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- mitochondrial degradation, retinal ganglion cell axons, optic nerve head, astrocytes, axonal mitochondria, lysosomes, neuronal mitochondria
- MeSH terms
- Red Fluorescent Protein, Animals, Astrocytes, Axons, Exocytosis, Immunohistochemistry, Luminescent Proteins, Lysosomes, Optic Disk, Phagocytosis, Retinal Ganglion Cells, In Situ Hybridization, Fluorescence, In Situ Nick-End Labeling, Imaging, Three-Dimensional, Mice, Electron Microscope Tomography, Mitophagy
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