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PMID: 12153478 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Stimulatory effect of vitamin C on autophagy in glial cells.

Journal of neurochemistry ·Vol. 82 ·No. 3 ·2002-08-00 ·Pages 538-49

Martin A, Joseph JA, Cuervo AM

Abstract

Intracellular accumulation of damaged or abnormal proteins is a common event associated with numerous neurodegenerative diseases and other age-related pathologies. Increasing the activity of the intracellular proteolytic systems normally responsible for the removal of these abnormal proteins might be beneficial in lessening the severity or development of those pathologies. In this study we have used human astrocyte glial cells to investigate the effect of vitamin C (ascorbate) on the intracellular turnover of proteins. Supplementation of the culture medium with physiological concentrations of vitamin C did not affect protein synthesis, but did increase the rate of protein degradation by lysosomes. Vitamin C accelerated the degradation of intra- and extracellular proteins targeted to the lysosomal lumen by autophagic and heterophagic pathways. At the doses analyzed, vitamin C lowered and stabilized the acidic intralysosomal pH at values that result in maximum activation of the lysosomal hydrolases.

MeSH Terms
Ascorbic Acid/pharmacokinetics,pharmacology Astrocytes/chemistry,cytology,drug effects,metabolism Cell Line Dose-Response Relationship, Drug Enzyme Activation/drug effects Humans Lysosomes/chemistry,drug effects,enzymology Neuroglia/chemistry,cytology,drug effects,metabolism Peptide Hydrolases/metabolism Proteins/metabolism
Chemicals
Proteins Peptide Hydrolases Ascorbic Acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Martin Antonio
Neuroscience Laboratory, HNRC on Aging, Tufts University, Boston, Massachusetts, USA.
Joseph James A
Cuervo Ana Maria
Article Info
Journal
Journal of neurochemistry
Abbr.
J Neurochem
ISSN
0022-3042
Published
2002-08-00
Pages
538-49
Language
English
Region
England
NLM ID
2985190R
Subset
IM
Grants
NIA NIH HHS · AG-029K01 · United States
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