Literature DB >> 11707918

Oxidative stress, aging and the proteasomal system.

T Grune1.   

Abstract

Oxygen free radicals and other oxidants are causing potential danger for intracellular proteins during the lifetime of cells and organisms. Therefore, protein oxidation is one of the natural consequences of aerobic life. The degradation of non-functional, oxidized proteins is an essential part of the antioxidant defenses of cells. The major proteolytic system responsible for the removal of oxidized cytosolic proteins is the proteasomal system. This system consists of the 20S 'core' proteasome and a multitude of various regulators. It is known that certain components of this system are regulated during oxidative stress and aging. One of the highlights of age-related changes of cellular metabolism is the accumulation of oxidized proteins. The question whether the accumulation of oxidized proteins during aging is due to a malfunction of the intracellular proteolytic machinery of the cell remains still unsolved. The information available about an age-related decline of the proteasomal system is very contradictory. The current literature about the proteasomal system, the regulation of this system during oxidative stress and the age-related changes are in the focus of this review.

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Year:  2000        PMID: 11707918     DOI: 10.1023/a:1010037908060

Source DB:  PubMed          Journal:  Biogerontology        ISSN: 1389-5729            Impact factor:   4.277


  35 in total

1.  Mild heat stress stimulates 20S proteasome and its 11S activator in human fibroblasts undergoing aging in vitro.

Authors:  Rasmus Beedholm; Brian F C Clark; Suresh I S Rattan
Journal:  Cell Stress Chaperones       Date:  2004-03       Impact factor: 3.667

2.  Activation of chaperone-mediated autophagy during oxidative stress.

Authors:  Roberta Kiffin; Christopher Christian; Erwin Knecht; Ana Maria Cuervo
Journal:  Mol Biol Cell       Date:  2004-08-25       Impact factor: 4.138

3.  Nrf2, a guardian of healthspan and gatekeeper of species longevity.

Authors:  Kaitlyn N Lewis; James Mele; John D Hayes; Rochelle Buffenstein
Journal:  Integr Comp Biol       Date:  2010-05-06       Impact factor: 3.326

4.  Effects of aging and dietary restriction on ubiquitination, sumoylation, and the proteasome in the spleen.

Authors:  Le Zhang; Feng Li; Edgardo Dimayuga; Jeffrey Craddock; Jeffrey N Keller
Journal:  FEBS Lett       Date:  2007-11-06       Impact factor: 4.124

5.  Changes in the activity of proteasomes in vivo induced by oxidative stress or para-aminobenzoic acid in loach embryos.

Authors:  N P Sharova; O G Stroeva; P A Erokhov; S B Dmitrieva; T A Usova
Journal:  Dokl Biochem Biophys       Date:  2007 Jul-Aug       Impact factor: 0.788

6.  Hormetic modulation of aging and longevity by mild heat stress.

Authors:  Suresh I S Rattan
Journal:  Dose Response       Date:  2006-05-22       Impact factor: 2.658

7.  Aging and dietary restriction effects on ubiquitination, sumoylation, and the proteasome in the heart.

Authors:  Feng Li; Le Zhang; Jeffrey Craddock; Annadora J Bruce-Keller; Kalavathi Dasuri; AnhThao Nguyen; Jeffrey N Keller
Journal:  Mech Ageing Dev       Date:  2008-04-30       Impact factor: 5.432

8.  Molecular mechanisms of anti-aging hormetic effects of mild heat stress on human cells.

Authors:  Suresh I S Rattan; Yvonne E G Eskildsen-Helmond; Rasmus Beedholm
Journal:  Nonlinearity Biol Toxicol Med       Date:  2004-04

Review 9.  Carbonyl stress in aging process: role of vitamins and phytochemicals as redox regulators.

Authors:  Volkan Ergin; Reza Ebrahimi Hariry; Cimen Karasu
Journal:  Aging Dis       Date:  2013-10-01       Impact factor: 6.745

10.  Tau protein degradation is catalyzed by the ATP/ubiquitin-independent 20S proteasome under normal cell conditions.

Authors:  Tilman Grune; Diana Botzen; Martina Engels; Peter Voss; Barbara Kaiser; Tobias Jung; Stefanie Grimm; Gennady Ermak; Kelvin J A Davies
Journal:  Arch Biochem Biophys       Date:  2010-05-15       Impact factor: 4.013

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