Effect of oxidant systems on the ubiquitylation of proteins in the central nervous system

Ana M. Adamo, Laura A. Pasquini, Marcos Besio Moreno, Patricia I. Oteiza, Eduardo F. Soto, Juana M. Pasquini

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Ubiquitin (Ub) modification of different proteins plays an important role in many cellular processes. However, the best studied function of Ub is the labeling of proteins committed to rapid degradation, by an ATP-dependent pathway. We previously found that this pathway is operative in the central nervous system (CNS) of adult rats (Adamo et al. [1994] J. Neurosci. Res. 38:358-364). In the present study, we examined the changes in the capacity to form high-molecular-weight Ub protein conjugates (UbPC) and the changes in the production of 2-thiobarbituric acid-reactive substances (TBARS), in the content of protein-associated carbonyl groups (PAC), and in the activity of glutamine synthetase produced by in vitro peroxidation of the cell cytosolic proteins and of the mitochondrial fraction isolated from rat brain. Under these experimental conditions, there was an increase in PAC and TBARS in the cytosol, indicating that damage to certain cellular components had occurred. Simultaneously there was a marked increase in UbPC in comparison with the nonoxidized controls. These conjugates showed an active turnover and accumulated when Ub-mediated proteolysis was inhibited. In vitro peroxidation of the mitochondrial fractions resulted in an increase in the production of PAC and in an enhancement in the formation of UbPC. These results demonstrate that the oxidized proteins can be recognized by the ubiquitylating system and that in the CNS the Ub-dependent proteolytic pathway is one of the possible mechanisms involved in the removal of cytosolic and mitochondrial fraction damaged proteins.

Original languageEnglish (US)
Pages (from-to)523-531
Number of pages9
JournalJournal of Neuroscience Research
Volume55
Issue number4
DOIs
StatePublished - Feb 15 1999
Externally publishedYes

Fingerprint

Ubiquitination
Oxidants
Central Nervous System
Ubiquitin
Proteins
Thiobarbituric Acid Reactive Substances
Glutamate-Ammonia Ligase
Mitochondrial Proteins
Cytosol
Proteolysis
Adenosine Triphosphate
Molecular Weight

Keywords

  • Oxidative stress
  • Proteasome
  • Protein peroxidation
  • Proteolysis
  • Ubiquitin

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Effect of oxidant systems on the ubiquitylation of proteins in the central nervous system. / Adamo, Ana M.; Pasquini, Laura A.; Moreno, Marcos Besio; Oteiza, Patricia I.; Soto, Eduardo F.; Pasquini, Juana M.

In: Journal of Neuroscience Research, Vol. 55, No. 4, 15.02.1999, p. 523-531.

Research output: Contribution to journalArticle

Adamo, Ana M. ; Pasquini, Laura A. ; Moreno, Marcos Besio ; Oteiza, Patricia I. ; Soto, Eduardo F. ; Pasquini, Juana M. / Effect of oxidant systems on the ubiquitylation of proteins in the central nervous system. In: Journal of Neuroscience Research. 1999 ; Vol. 55, No. 4. pp. 523-531.
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