RRC ID |
12766
|
著者 |
Shimizu N, Yoshikawa N, Ito N, Maruyama T, Suzuki Y, Takeda S, Nakae J, Tagata Y, Nishitani S, Takehana K, Sano M, Fukuda K, Suematsu M, Morimoto C, Tanaka H.
|
タイトル |
Crosstalk between glucocorticoid receptor and nutritional sensor mTOR in skeletal muscle.
|
ジャーナル |
Cell Metab
|
Abstract |
Maintenance of skeletal muscle mass relies on the dynamic balance between anabolic and catabolic processes and is important for motility, systemic energy homeostasis, and viability. We identified direct target genes of the glucocorticoid receptor (GR) in skeletal muscle, i.e., REDD1 and KLF15. As well as REDD1, KLF15 inhibits mTOR activity, but via a distinct mechanism involving BCAT2 gene activation. Moreover, KLF15 upregulates the expression of the E3 ubiquitin ligases atrogin-1 and MuRF1 genes and negatively modulates myofiber size. Thus, GR is a liaison involving a variety of downstream molecular cascades toward muscle atrophy. Notably, mTOR activation inhibits GR transcription function and efficiently counteracts the catabolic processes provoked by glucocorticoids. This mutually exclusive crosstalk between GR and mTOR, a highly coordinated interaction between the catabolic hormone signal and the anabolic machinery, may be a rational mechanism for fine-tuning of muscle volume and a potential therapeutic target for muscle wasting.
|
巻・号 |
13(2)
|
ページ |
170-82
|
公開日 |
2011-2-2
|
DOI |
10.1016/j.cmet.2011.01.001
|
PII |
S1550-4131(11)00002-7
|
PMID |
21284984
|
MeSH |
Animals
Kruppel-Like Transcription Factors / metabolism
Mice
Muscle Proteins / metabolism
Muscle, Skeletal / metabolism*
Protein Binding
Rats
Receptors, Glucocorticoid / genetics
Receptors, Glucocorticoid / metabolism*
Repressor Proteins / metabolism
SKP Cullin F-Box Protein Ligases / metabolism
TOR Serine-Threonine Kinases / metabolism*
Transcription Factors
Transcription, Genetic
Ubiquitin-Protein Ligases / metabolism
|
IF |
21.567
|
引用数 |
227
|
WOS 分野
|
ENDOCRINOLOGY & METABOLISM
CELL BIOLOGY
|
リソース情報 |
遺伝子材料 |
Ax1 CA gfp (RDB01727) |