Mitochondrial adaptations in skeletal muscle to hindlimb unloading

被引:52
作者
Wagatsuma, Akira [1 ]
Kotake, Naoki [2 ]
Kawachi, Takayuki [1 ]
Shiozuka, Masataka [1 ]
Yamada, Shigeru [1 ]
Matsuda, Ryoichi [1 ]
机构
[1] Univ Tokyo, Dept Life Sci, Grad Sch Arts & Sci, Meguro Ku, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Engn, Dept Adv Interdisciplinary Studies, Meguro Ku, Tokyo, Japan
关键词
Adaptation; Atrophy; Hindlimb unloading; Mitochondria; Skeletal muscle; ACTIVATED RECEPTOR-ALPHA; SOLEUS MUSCLE; OXIDATIVE STRESS; RAT SOLEUS; TRANSCRIPTIONAL CONTROL; COACTIVATOR PGC-1; GENE-EXPRESSION; HYPOKINESIA-HYPODYNAMIA; SUSPENSION HYPOKINESIA; GLUCOSE-UPTAKE;
D O I
10.1007/s11010-010-0677-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To gain insight into the regulation of mitochondrial adaptations to hindlimb unloading (HU), the activity of mitochondrial enzymes and the expression of nuclear-encoded genes which control mitochondrial properties in mouse gastrocnemius muscle were investigated. Biochemical and enzyme histochemical analysis showed that subsarcolemmal mitochondria were lost largely than intermyofibrillar mitochondria after HU. Gene expression analysis revealed disturbed or diminished gene expression patterns. The three main results of this analysis are as follows. First, in contrast to peroxisome proliferator-activated receptor gamma coactivator 1 beta (PGC-1 beta) and PGC-1-related coactivator, which were down-regulated by HU, PGC-1 alpha was up-regulated concomitant with decreased expression of its DNA binding transcription factors, PPAR alpha, and estrogen-related receptor alpha (ERR alpha). Moreover, there was no alteration in expression of nuclear respiratory factor 1, but its downstream target gene, mitochondrial transcription factor A, was down-regulated. Second, both mitofusin 2 and fission 1, which control mitochondrial morphology, were down-regulated. Third, ATP-dependent Lon protease, which participates in mitochondrial-protein degradation, was also down-regulated. These findings suggest that HU may induce uncoordinated expression of PGC-1 family coactivators and DNA binding transcription factors, resulting in reducing ability of mitochondrial biogenesis. Furthermore, down-regulation of mitochondrial morphology-related genes associated with HU may be also involved in alterations in intracellular mitochondrial distribution.
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页码:1 / 11
页数:11
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