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The antioxidant requirement for plasma membrane repair in skeletal muscle.
Free Radical Biol. Med. 84, 246-253 (2015)
Vitamin E (VE) deficiency results in pronounced muscle weakness and atrophy but the cell biological mechanism of pathology is unknown. We previously showed that VE supplementation promotes membrane repair in cultured cells and that oxidants potently inhibit repair. Here we provide three independent lines of evidence that VE is required for skeletal muscle myocyte plasma membrane repair in vivo. We also show that when another lipid-directed antioxidant, glutathione peroxidase 4 (Gpx4), is genetically deleted in mouse embryonic fibroblasts, repair fails catastrophically, unless cells are supplemented with VE. We conclude that lipid-directed antioxidant activity provided by VE, and possibly also Gpx4, is an essential component of the membrane repair mechanism in skeletal muscle. This work explains why VE is essential to muscle health and identifies VE as a requisite component of the plasma membrane repair mechanism in vivo.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
5.736
1.641
23
28
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Antioxidants ; Free Radicals ; Membrane Repair ; Skeletal Muscle ; Vitamin E; Hydroperoxide Glutathione-peroxidase; Frog Neuromuscular-junction; Vitamin-e Supplementation; Muscular-dystrophy; Oxidative Stress; E-deficiency; Exercise; Damage; Disruptions; Myopathy
Sprache
englisch
Veröffentlichungsjahr
2015
HGF-Berichtsjahr
2015
ISSN (print) / ISBN
0891-5849
e-ISSN
1873-4596
Zeitschrift
Free Radical Biology and Medicine
Quellenangaben
Band: 84,
Seiten: 246-253
Verlag
Elsevier
Verlagsort
New York, NY
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Developmental Genetics (IDG)
POF Topic(s)
30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
Forschungsfeld(er)
Genetics and Epidemiology
PSP-Element(e)
G-500500-004
WOS ID
WOS:000355896500022
Scopus ID
84928943708
PubMed ID
25843658
Erfassungsdatum
2015-04-08