A FoxO1-dependent, but NRF2-independent induction of heme oxygenase-1 during muscle atrophy.

Abstract:

:Skeletal muscle plays key roles in metabolic homeostasis. Loss of muscle mass, called muscle atrophy exacerbates disease-associated metabolic perturbations. In this study, we characterized the molecular functions and mechanisms underlying regulation of skeletal muscle atrophy induced by denervation. Denervation significantly increased the expression of heme oxygenase-1 (HO-1) and atrogenes in skeletal muscle. Forkhead box protein O1 (FoxO1) drastically increased in atrophied muscle and selectively stimulated HO-1 gene transcription through direct DNA binding. Lack of HO-1 substantially attenuated muscle atrophy, whereas HO-1 overexpression caused muscle damage in vitro and in vivo. Collectively, HO-1 induced by FoxO1 may cause skeletal muscle atrophy.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Kang J,Jeong MG,Oh S,Jang EJ,Kim HK,Hwang ES

doi

10.1016/j.febslet.2013.11.009

subject

Has Abstract

pub_date

2014-01-03 00:00:00

pages

79-85

issue

1

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(13)00843-0

journal_volume

588

pub_type

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