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PMID: 8512210 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

The lysosomal system in neuronal cell death: a review.

Annals of the New York Academy of Sciences ·Vol. 679 ·1993-05-28 ·Pages 87-109

Nixon RA, Cataldo AM

Abstract

The lysosomal system has often been considered a prominent morphologic marker of distressed or dying neurons. Lysosomes or their constituent hydrolases have been viewed in different neuropathologic states as either initiators and direct agents of cell death, agents of cellular repair and recompensation, effectors of end-stage cellular dissolution, or autolytic scavengers of cellular debris. Limited data and limitations of methodology often do not allow these potential roles to be discriminated. In all forms of neurodegeneration, it may be presumed that lysosomes ultimately rupture and release various hydrolases that promote cell autolysis during the final stages of cellular disintegration. Beyond this perhaps universal contribution to cell death, the degree to which the lysosomal system may be involved in neurodegenerative states varies considerably. In many conditions, morphologic evidence for activation of the lysosomal system is minimal or undetectable. In other cases, lysosomal activation is evident only when other morphologic signs of cell injury are also present. This level of participation may be viewed as either an attempt by the neuron to compensate for or repair the injury or a late-stage event leading to cell dissolution. The early involvement of the lysosomal system in neurodegeneration occurs most commonly in the form of intraneuronal accumulations of abnormal storage profiles or residual bodies (tertiary lysosomes). Very often the lysosomal involvement can be traced to a primary defect or dysfunction of lysosomal components or to accelerated or abnormal membrane breakdown that leads to the buildup of modified digestion-resistant substrates within lysosomes. Because they are often striking, changes in the lysosomal system are a sensitive morphologic indicator of certain types of metabolic distress; however, whether they reflect a salutary response of a compromised neuron or a mechanism to promote cell death and removal of debris from the brain remains to be established for most conditions. Factors that may influence the lysosomal response during lethal neuronal injury include species differences, stage of neuronal development, duration of injury and pace of cell death. The lysosomal system may be more closely coupled to certain forms of neuronal cell death in lower vertebrate or invertebrate systems than in mammalian systems.

MeSH Terms
Animals Biomarkers Cell Death/physiology Endopeptidases/metabolism Humans Hydrolases/metabolism Lysosomes/enzymology Models, Neurological Nervous System Diseases/enzymology,pathology Neurons/cytology,enzymology,pathology
Chemicals
Biomarkers Hydrolases Endopeptidases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Nixon R A
Laboratories for Molecular Neuroscience, Mailman Research Center, McLean Hospital, Belmont, Massachusetts 02178.
Cataldo A M
Article Info
Journal
Annals of the New York Academy of Sciences
Abbr.
Ann N Y Acad Sci
ISSN
0077-8923
Published
1993-05-28
Pages
87-109
Language
English
Region
United States
NLM ID
7506858
Subset
IM
Grants
NIA NIH HHS · AG05134 · United States
NIA NIH HHS · AG08208 · United States
NIA NIH HHS · AG10916 · United States
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