Cited by 680Autophagy in Disease and TherapyMitochondrial Function and PathologyCellular transport and secretion

Transcellular degradation of axonal mitochondria

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Davis, Chung-ha O., Kim, Keun-Young, Bushong, Eric A., Mills, Elizabeth A., Boassa, Daniela, Shih, Tiffany, Kinebuchi, Mira, Phan, Sebastien +6 more·2014·Proceedings of the National Academy of Sciences

Abstract

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.

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Crossref · 10.1073/pnas.1404651111

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  • Cells with mitochondrial defects might release damaged mitochondria to be picked up by other cells, facilitating degradation by recipient cells.

    “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]

    The Significance section and Discussion report that retinal ganglion cell axons shed mitochondria that adjoining astrocytes take up and degrade. The study describes otherwise healthy axons in wild-type mice; it does not establish that the releasing cells had mitochondrial defects or that the shed mitochondria were damaged. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Degradation of neuronal mitochondria can occur non-cell autonomously, as demonstrated by astrocytic engulfment and degradation of mitochondria excreted from retinal ganglion cells.

    “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].”

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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;
Venue
Proceedings of the National Academy of Sciences
Published
2014-06-16
Volume
111
Issue
26
Pages
9633-9638
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
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
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
  • Health Sciences › Medicine › Epidemiology › 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

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