Inhibition of muscle insulin-like growth factor I expression by tumor necrosis factor-α

被引:68
作者
Fernández-Celemín, L [1 ]
Pasko, N [1 ]
Blomart, V [1 ]
Thissen, JP [1 ]
机构
[1] Catholic Univ Louvain, DIAB 5474, Unite Diabetol & Nutr, B-1200 Brussels, Belgium
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2002年 / 283卷 / 06期
关键词
skeletal muscle; lipopolysaccharide; C2C12; cells;
D O I
10.1152/ajpendo.00054.2002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The role of TNF-alpha in muscle catabolism is well established, but little is known about the mechanisms of its catabolic action. One possibility could be that TNF-alpha impairs the production of local growth factors like IGF-I. The aim of this study was to investigate whether TNF-alpha can directly inhibit IGF-I gene and protein expression in muscle. First, we investigated whether the acute inflammation induced by endotoxin injection changes IGF-I and TNF-alpha mRNA in rat tibialis anterior muscle. Endotoxin rapidly increased TNF-alpha mRNA (7-fold at 1 h, P < 0.001) and later decreased IGF-I mRNA (-73% at 12 h, P < 0.001). Furthermore, in a model of C2C12 myotubes, TNF-alpha strongly inhibited IGF-I mRNA and protein (-73 and -47% after 72 h, P < 0.001 and P < 0.01, respectively). Other proinflammatory cytokines failed to inhibit IGF-I mRNA. The effect of TNF-alpha on IGF-I mRNA was not mediated by nitric oxide, and the activation of NF-kappaB was insufficient to inhibit IGF-I expression. Taken together, our data suggest that TNF-alpha induced in muscle after LPS injection can locally inhibit IGF-I expression. The inhibition of muscle IGF-I production could contribute to the catabolic effect of TNF-alpha.
引用
收藏
页码:E1279 / E1290
页数:12
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