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
Cited by
Sorted by citations
Items 501–600 of 679
Vesicle-guided mitochondria: A new perspective for brain mitochondrial transplantation
Girgenti, A., Palumbo, L., Kubat, G. B., Türkel, İ., Picone, P., & Nuzzo, D. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102881 · Cited by 6
Mitochondrial transfer in the HSC–HCC–macrophage network shapes hepatocellular carcinoma progression
Zhang, L., Ren, C., He, M., Chen, X., Liu, H., Liu, Y., Luo, J., Li, Z. H. U., Wang, J., Miao, W., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2512592123 · Cited by 6
Marzetti, E., Lorenzo, R. D., Calvani, R., Coelho‐Júnior, H. J., D’Argento, E., Pesce, V., Landi, F., Bucci, C., Guerra, F., & Picca, A. (2026) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2026.112167 · Cited by 8
Huang, S., Huang, P., Yu, H., Chen, J., Liu, X., Wang, J., Shen, X. P., & Zhong, Y. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03640-x · Cited by 6
Bao, F., Zhou, L., Xiao, J., & Liu, X. (2022) · Biochemical Society Transactions · doi:10.1042/bst20220726 · Cited by 6
Ariosa, A., & Klionsky, D. J. (2015) · Autophagy · doi:10.1080/15548627.2015.1009790 · Cited by 6
Q&A: Trash talk: disposal and remote degradation of neuronal garbage
Arnold, M. L., Melentijevic, I., Smart, A. J., & Driscoll, M. (2018) · BMC Biology · doi:10.1186/s12915-018-0487-6 · Cited by 6
iPSCs-derived mesenchymal stromal cells mitigate anxiety and neuroinflammation in aging female mice
Wei, X., Li, R., Li, X., Wang, B., Huang, J., Mu, H., Zhang, Q., Zhang, Z., Ru, Y., Wu, X., et al. (2022) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2022.106347 · Cited by 6
Mitochondrion in Pulmonary Disease: Small Organelle but Big Function
Wang, J., Wu, H., Gao, J., & Zhang, T. (2025) · Small Methods · doi:10.1002/smtd.202500674 · Cited by 5
Cross-Organ Mitochondrial Communication in Stress and Disease
Shen, K., Durieux, J., & Dillin, A. G. (2025) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-062124-024150 · Cited by 5
Mitochondrial transplant: Unravelling a promising treatment for ocular diseases
Yeo, Y., Bhargava, M., Khare, R. S., Parikh, B. H., & Su, X. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103902 · Cited by 6
Neuron–Glia Crosstalk in the Regulation of Astrocytic Antioxidative Mechanisms Following CNS Injury
Zakrzewski, P. K., & Boczek, T. (2025) · Antioxidants · doi:10.3390/antiox14121415 · Cited by 10
Intercellular mitochondrial transfer: A novel neuroprotective strategy in stroke management
Piao, X., Tang, X., Li, L., Zhang, Y., & Li, H. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.178433 · Cited by 5
D’Ambrosio, L., Greco, M. E., Forte, M., Vecchio, D., Schiavon, S., Nonno, F. D., Tahir, S., Picchio, V., Cozzolino, C., Sarto, G., et al. (2025) · Biology Direct · doi:10.1186/s13062-025-00703-1 · Cited by 6
Extracellular vesicles and mitochondria in central nervous system diseases
Park, J.-H., Back, D. J., Hamanaka, G., Ishikane, S., & Hayakawa, K. (2025) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x251399018 · Cited by 5
Li, S., Wang, M., Zhou, H., Liu, J., Wang, M., Yuan, H., Zheng, M., Li, X., Zhu, X., & Xiang, M. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103996 · Cited by 7
Inaba, T., Miyamoto, N., Hira, K., Kijima, C., Miyauchi, Y., Xu, H., Kanazawa, K., Yuji, U. E. N. O., & Hattori, N. (2026) · MedComm · doi:10.1002/mco2.70590 · Cited by 6
Mitochondria transfer in glioblastoma
Storevik, S., Augustsson, M. T., Moreino, S. S., Köppe, H., Watson, D. C., Bayık, D., Fernandez, C. D. L. P., Serapiglia, A. M., Panicker, N., Lathia, J. D., et al. (2026) · Neuro-Oncology · doi:10.1093/neuonc/noag038 · Cited by 5
Sternberg, Z. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03684-2 · Cited by 6
Li, S., Wang, D., Liu, D.-H., Meng, X., Wang, Z., Guo, X., Liu, Q., Liu, P., Li, S., Wang, S., et al. (2024) · MedComm · doi:10.1002/mco2.568 · Cited by 5
Mitochondrial Transfer in the Neurovascular Unit, Not Only for Energy Rescue: A Systematic Review
Zhou, D., Yang, S., Wu, J., Li, Y., Jin, H., Luo, Y., Zhang, F., Jiang, J., Hu, B., & Zhou, Y. (2024) · Aging and Disease · doi:10.14336/ad.2024.0461 · Cited by 5
Self-citationEzan, P., Hardy, E., Bemelmans, A., Taiel, M., Dossi, E., & Rouach, N. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106681 · Cited by 5
Neuroglial Crosstalk by Mitochondria
Ho, M. S.-C. (2016) · Neuroscience Bulletin · doi:10.1007/s12264-016-0072-3 · Cited by 5
Single-Cell Dissociation and Characterization in the Murine Retina and Optic Nerve
Choi, H. J., Wang, R., & Jakobs, T. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7407-8_21 · Cited by 5
Mitochondrial Transfer: From Bench to Bedside
Ikeda, G., Li, J., Wang, A., Paleru, A. M., & Yang, P. C.-M. (2026) · Circulation Research · doi:10.1161/circresaha.125.326984 · Cited by 6
Semyanov, A. V., & Verkhratsky, A. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00002-4 · Cited by 5
Irrational lighting as a health risk occurring in the Arctic
Va, K. (2020) · Health Risk Analysis · doi:10.21668/health.risk/2020.1.18.eng · Cited by 4
Cell-specific mitochondrial response in progressive supranuclear palsy
Sackmann, V., Nassir, N., Tanikawa, S., Forrest, S. L., Chasiotis, H., Li, J., Hanif, S., Martínez-Valbuena, I., Tartaglia, M. C., Lang, A. E., et al. (2025) · Mitochondrion · doi:10.1016/j.mito.2025.102043 · Cited by 4
Optical manipulation of neuronal mitochondria using scanning optical tweezers
Gong, Z., Wu, T., Chen, X., Wang, P., Guo, J., Li, Y., & Li, B. (2023) · Journal of Innovative Optical Health Sciences · doi:10.1142/s1793545823410018 · Cited by 4
Wang, G., Guasp, R. J., Salam, S., Chuang, E., Morera, A., Smart, A. J., Jimenez, D., Shekhar, S., Friedman, E., Melentijevic, I., et al. (2024) · eLife · doi:10.7554/elife.95443 · Cited by 9
Mitochondria at the Base of Neuronal Innate Immunity in Alzheimer’s and Parkinson’s Diseases
Esteves, A. R., Silva, D. F., Santos, D., Candeias, E., Filipe, F., & Cardoso, S. M. (2018) · InTech eBooks · doi:10.5772/intechopen.72612 · Cited by 4
MeCP2 at the crossroads of hypoxia, oxidative stress, and gene regulation in Rett syndrome
Huang, J. L., Sharifi, O., Yasui, D. H., & LaSalle, J. M. (2025) · Epigenomics · doi:10.1080/17501911.2025.2568303 · Cited by 3
Intercellular mitochondrial transfer and trans-mitophagy in response to protein import dysfunction
Glover, E., Wiseman, B., Dugdale, C. A., Humphery, C., Ballesteros, L. S., Hodgson, L. R., Wilkinson, K. A., & Collinson, I. R. (2026) · The Journal of Cell Biology · doi:10.1083/jcb.202511211 · Cited by 3
Sardari, M., Sahafi, O. H., & Rezayof, A. (2025) · Brain Research · doi:10.1016/j.brainres.2025.150040 · Cited by 3
Arumugam, P., Heim, C. E., Fallet, R. W., Shinde, D., Thomas, V. C., Argüello, R. J., & Kielian, T. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117057 · Cited by 3
Rethinking Mitochondria: The Extracellular Dimension
Pena-Couso, L., Makuch, M., & Nicolás-Ávila, J. Á. (2026) · Circulation Research · doi:10.1161/circresaha.125.326988 · Cited by 4
Maddineni, P., Kaipa, B. R., Kodati, B., Kesavan, K., Li, L., Millar, J. C., Yacoub, S., Kasetti, R. B., Clark, A. F., & Zode, G. S. (2026) · Molecular Neurodegeneration · doi:10.1186/s13024-026-00950-4 · Cited by 4
Mitochondria and brain aging: From cell-specific dysfunction to intercellular cooperation
Grimm, A., Lang, U. E., & Eckert, A. (2026) · Neuron · doi:10.1016/j.neuron.2026.04.048 · Cited by 4
Irrational lighting as a health risk occurring in the Arctic
Kaptsov, V. A., & Deinego, V. N. (2020) · Health Risk Analysis · doi:10.21668/health.risk/2020.1.18 · Cited by 3
β2-glycoprotein I promotes the clearance of circulating mitochondria
Dasgupta, S. K., Gollamudi, J., Rivera, S., Poché, R. A., Rumbaut, R. E., & Thiagarajan, P. (2024) · PLoS ONE · doi:10.1371/journal.pone.0293304 · Cited by 3
Retrolaminar Demyelination of Structurally Intact Axons in Nonhuman Primate Experimental Glaucoma
Chaudhary, P., Lockwood, H., Stowell, C., Bushong, E. A., Reynaud, J. F., Yang, H., Gardiner, S. K., Williams, G. A., Williams, I., Ellisman, M. H., et al. (2024) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.65.2.36 · Cited by 4
Self-citationYang, S. S., Brooks, N. A. H., Silva, D. E. D., Gibon, J., Islam, H., & Klegeris, A. (2025) · Purinergic Signalling · doi:10.1007/s11302-025-10066-x · Cited by 3
Kaur, K. K., Allahbadia, G., & Singh, M. (2021) · Journal of Diabetes Metabolic Disorders & Control · doi:10.15406/jdmdc.2021.08.00228 · Cited by 2
Rapid isolation of intact retinal astrocytes: a novel approach
Cullen, P. F., Mazumder, A. G., Sun, D., & Flanagan, J. G. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01641-7 · Cited by 3
Autophagy Driven Extracellular Vesicles in the Leukaemic Microenvironment
Horton, R. H., Wileman, T., & Rushworth, S. A. (2020) · Current Cancer Drug Targets · doi:10.2174/1568009620666200428111051 · Cited by 3
Egorova, A. V., Воронков, Д. Н., Fedorova, E. N., Baranich, T. I., Glinkina, V. V., & Sukhorukov, V. S. (2022) · CLINICAL AND EXPERIMENTAL MORPHOLOGY · doi:10.31088/cem2023.12.2.5-13 · Cited by 9
King, L., & Plun‐Favreau, H. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803783-6.00005-5 · Cited by 6
Selective Autophagy as a Potential Therapeutic Target in Age-Associated Pathologies
Papandreou, M., & Tavernarakis, N. (2021) · Metabolites · doi:10.3390/metabo11090588 · Cited by 3
Fu, H., Li, J., Du, P., Jin, W., & Cui, D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/699405 · Cited by 2
A retrograde transit filter mediated by optineurin controls mitostasis in distal axonsPreprint
Marahori, N. A., Gailer, B., Schifferer, M., Kleele, T., Iatroudi, A., Hannan, S. B., Avramopoulos, P., Engelhardt, S. H., Lakadamyali, M., Brill, M. S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.28.604753 · Cited by 4
High Autophagy Patterns in Swelling Platelets During Apheresis Platelet Storage
Yu, L., Yu, S., He, Y., Deng, G., & Li, Q. (2023) · Indian Journal of Hematology and Blood Transfusion · doi:10.1007/s12288-023-01638-1 · Cited by 2
Unlocking extracellular mitochondria from bench to clinical application in stroke
Hamanaka, G., Back, D.-B., Park, J.-H., Ishikane, S., & Hayakawa, K. (2025) · Stem Cells Translational Medicine · doi:10.1093/stcltm/szaf060 · Cited by 2
Kramer, J., Rohwer, E., Sethu, P., Xie, M., Lee, T. C., Darley-Usmar, V. M., & Zhang, J. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.11.030 · Cited by 2
Shanmughapriya, S., Ahooyi, T. M., Torkzaban, B., Garikipati, V. N. S., Kishore, R., Khallili, K., Langford, D., & Natarajaseenivasan, K. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02589-y · Cited by 3
Jiang, M., Zhang, K., Li, M., Tian, Y., Wang, T., Rodríguez, R. A., Lin, Z., Meng, J., Li, C., Wang, Z., et al. (2026) · Molecular Cancer · doi:10.1186/s12943-026-02615-8 · Cited by 4
Mitophagy-mediated immune evasion: Shared strategies of pathogens
Li, J., Li, W., (34472), D. W., & Liu, Y. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104247 · Cited by 2
A big picture of the mitochondria-mediated signals: From mitochondria to organism
Acar, N. V., & Özgül, R. K. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.08.032 · Cited by 2
Mitochondrial Treatment Improves Cognitive Impairment Induced by Lipopolysaccharide in Mice
Yan, Q., Liu, T., Liu, L., Wei, Y., Zhao, Y., Yu, C., Zhong, Z.-G., Huang, J.-L., & Wu, D. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04368-1 · Cited by 2
Pakkarato, S., Thoungseabyoun, W., Tachow, A., Rawangwong, A., Kagawa, Y., Owada, Y., Kondo, H., & Hipkaeo, W. (2016) · Anatomical Science International · doi:10.1007/s12565-016-0370-x · Cited by 2
Anti-oxidants in astrocytes as target of neuroprotection for Parkinson’s disease
Asanuma, M., & Miyazaki, I. (2020) · Folia Pharmacologica Japonica · doi:10.1254/fpj.20071 · Cited by 2
Anatomy and Physiology of optic nerve head
Li, X., & Wang, N. (2019) · Advances in visual science and eye diseases · doi:10.1007/978-981-13-2137-5_8 · Cited by 2
Mitochondrial biogenesis and mitophagy
Tan, S., Kennedy, B. K., & Wong, E. S. P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821562-3.00037-x · Cited by 2
Uspenskaya, Y. A., Malinovskaya, N. A., & Salmina, A. B. (2022) · Cell and Tissue Biology · doi:10.1134/s1990519x22020109 · Cited by 2
Optic nerve head: A gatekeeper for vitreous infectious insults?
Lai, W., Huang, J., Fang, W., Deng, S., Xie, Y., Wang, W., Qiao, T., Xu, G., Wang, X., & Ding, F. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.987771 · Cited by 3
Arnold, M. L., Cooper, J. F., Grant, B. D., & Driscoll, M. (2020) · Journal of Visualized Experiments · doi:10.3791/61368-v · Cited by 2
Platelets fuel mesenchymal stem cells by providing live mitochondria
Zhao, Z., Zhang, J., & Dong, J. (2021) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.15295 · Cited by 2
Energy Crisis after Inter-System Mitochondria Transfer is the Direct Cause of Death by SepsisPreprint
Tang, M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.01.505533 · Cited by 2
Wang, G., Guasp, R. J., Salam, S., Chuang, E., Morera, A., Smart, A. J., Jimenez, D., Shekhar, S., Melentijevic, I., Nguyen, K. C. Q., et al. (2024) · eLife · doi:10.7554/elife.95443.1 · Cited by 2
Maddineni, P., Kodati, B., Kaipa, B. R., Kesavan, K., Millar, J. C., Yacoub, S., Kasetti, R. B., Clark, A. F., & Zode, G. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.13.638142 · Cited by 3
aulestia, F. C. (2019) · theses.fr (ABES) · doi:10.70675/3b6b7bffz584fz4cd9z9d0az246c16c16ecd · Cited by 2
Powering Up the Brain: Intercellular Mitochondrial Quality Control and Its Implication in Stroke
Zhou, X., Wu, S., Huang, T., Li, Y., Yang, J., Gu, Z., & Zhang, X. (2025) · Current Neuropharmacology · doi:10.2174/011570159x388351250620065716 · Cited by 1
Impact of O ‐ GlcNAcylation Elevation on Mitophagy and Glia in the Dentate Gyrus
Kramer, J., Fu, S. Y., Ouyang, X., Rohwer, E., Chatham, J. C., Young, M. E., Darley-Usmar, V. M., & Zhang, J. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70205 · Cited by 1
Microglia maintain retinal redox homeostasis following ablation of rod photoreceptors in zebrafish
Morales, M., & Mitchell, D. M. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.113169 · Cited by 1
Cytokine and chemokine production by astrocytes is influenced by Cystatin C.
Palmer, A. L., Wang, R., Zonta, Y. R., Bailey, Z., Kuipers, H. F., & Ousman, S. (2025) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2025.578801
Interplay between extracellular vesicles and mitochondria
Coelho, P., & Pinheiro, P. S. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-29283-5.00004-2 · Cited by 1
Mitochondria in the immune system: Therapeutic potential from mitochondria transfer
Le, T. H. N., & Nguyen, V. T. T. (2025) · International Reviews of Immunology · doi:10.1080/08830185.2025.2577986 · Cited by 1
Mei, Z., Zhong, W., Deng, T., Meng, X., Lv, X., Xiao, J., & Li, Y. (2026) · Translational Stroke Research · doi:10.1007/s12975-025-01401-w · Cited by 1
Xu, Y., Li, J., Ma, S., Yang, T., Shen, Z., Li, M., & Huang, Q. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.01.053 · Cited by 1
Junuzović, M., Troillet, A., & Burk, J. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1763344 · Cited by 1
Neuroinflammation in glaucoma: a myriad of cellular pathways and players
MacLean, M., Lydon, S. D., Gomes, C., Pizzi, E. M., Diemler, C. A., Yablonski, S. E. R., Howell, G. R., Meyer, J. S., & Libby, R. T. (2026) · Mammalian Genome · doi:10.1007/s00335-026-10253-0 · Cited by 1
Horizontal transfer of mitochondria in cancer: The physiology reborn in disease?
Ayala, G., & Grelet, S. (2026) · Trends in Cell Biology · doi:10.1016/j.tcb.2026.06.003 · Cited by 1
Liu, X., Zhang, M., & Wang, Z. (2026) · Experimental Biology and Medicine · doi:10.3389/ebm.2026.11128 · Cited by 1
Free mitochondrial transfer enhances bone regeneration through cathepsin H mediated cysteine cycle
Diao, J., He, Q., Liu, Q., Liu, Y., Chen, S., Zhang, Y., Gui, H., Chen, J., wu, D., Pang, X., et al. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-03060-2 · Cited by 1
Sáenz‐de‐Santa‐María, I., Pepe, A., Tinévez, J.-Y., Brou, C., Vitrenko, Y. A., Cokelaer, T., Moyal, E. C., Weigert, R., & Zurzolo, C. (2026) · Nature Communications · doi:10.1038/s41467-026-76619-9 · Cited by 1
Moving mitochondria – Breathing new signaling into asthmatic airways
Nguyen, Q., & Shiva, S. (2018) · Redox Biology · doi:10.1016/j.redox.2018.07.013 · Cited by 1
Mitochondrial dynamics in neurodegenerative diseases
Su, B., Wang, X., Ju, G. A. O., & Qin, S. (2018) · Scientia Sinica Vitae · doi:10.1360/n052018-00157
Heatley, G. A., & Nickells, R. W. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-88442-6.00018-2 · Cited by 1
Astrocyte-Neuron Interactions Contributing to Amyotrophic Lateral Sclerosis Progression
Jensen, B. K. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-64839-7_12 · Cited by 1
Mitochondrial movement between mammalian cells: an emerging physiological phenomenon
Berridge, M. V., Herst, P. M., & Grasso, C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819656-4.00020-6 · Cited by 1
Neuronal Mitochondria are Different
Berman, S., & Hardwick, J. M. (2015) · Wiley eBooks · doi:10.1002/9781119017127.ch10 · Cited by 1
Mechanisms of Mitochondrial Dynamics
Serrat, R. (2019) · Wiley eBooks · doi:10.1002/9780470015902.a0028274 · Cited by 1
Lampinen, R., Belaya, I., Saveleva, L., Liddell, J. R., Rait, D., Huuskonen, M. T., Giniatullina, R., Sorvari, A., Soppela, L., Mikhailov, N., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.15.460570 · Cited by 1
Self-citationWang, G., Guasp, R. J., Salam, S., Chuang, E., Morera, A., Smart, A. J., Jimenez, D., Shekhar, S., Friedman, E., Melentijevic, I., et al. (2024) · eLife · doi:10.7554/elife.95443.2 · Cited by 1
Demonstration of the Feasibility of Mainstream Aging Theories and InterventionPreprint
Huang, B. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5151210 · Cited by 1
A study of mitochondrial biogenesis in the rodent nervous system
Desai, R. A. (2015) · UCL Discovery (University College London)
Axonal transport and life cycle of mitochondria in Parkinson's disease model
Sung, H. W. (2016) · Purdue e-Pubs (Purdue University System)
Axon Death Pathways Converge on Axed to Promote Axon Disassembly
Burdett, T. C. (2017) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/m2m89w
Emerging Connections: Synaptic Autophagy in Brain Aging and Disease
Liang, Y. (2018) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-319-98146-8_9
Serial Sectioning for 3D Imaging under Scanning Electron Microscopy
Luu, D. K. (2016) · TSpace (University of Toronto)
Skeletal muscle mitochondrial clearance
Leermakers (2019) · Research Publications (Maastricht University) · doi:10.26481/dis.20190405pl
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