Physiological activation of hypoxia inducible factor-1 in human skeletal muscle

被引:200
作者
Ameln, H [1 ]
Gustafsson, T
Sundberg, CJ
Okamoto, K
Jansson, E
Poellinger, L
Makino, Y
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, Sect Mol Exercise Physiol, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
[3] Karolinska Inst, Dept Lab Med, S-17177 Stockholm, Sweden
[4] Univ Tokyo, Inst Med Sci, Div Clin Immunol, Tokyo, Japan
关键词
exercise; gene expression; gene regulation; ischemia; angiogenesis;
D O I
10.1096/fj.04-2304fje
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human hypoxia inducible factor 1 (HIF-1) system is activated under various pathological conditions, yet less is known about its physiological regulation in healthy human tissue. We have studied the effect of exercise on the activation of HIF-1 in human skeletal muscle. Employing a model where oxygen consumption increases and oxygen tension can be manipulated, nine healthy male subjects performed 45 min of one-legged knee-extension exercise. Biopsies were taken before, directly after, and 30, 120, and 360 min after exercise. Exercise led to elevated HIF-1 alpha protein levels and a more prevalent nuclear staining of HIF-1 alpha. Interestingly, a concurrent decrease in von Hippel-Lindau tumor suppressor protein (VHL) levels was detected in some subjects. Moreover, exercise induced an increase in the DNA binding activity of HIF-1 alpha. Characterization of gene expression by real-time PCR demonstrated that the HIF-1 target genes VEGF and EPO were activated. VEGF mRNA was further increased when blood flow to the exercising leg was restricted. In conclusion, these data clearly demonstrate that physical activity induces the HIF-1-mediated signaling pathway in human skeletal muscle, providing the first evidence that human HIF-1 alpha can be activated during physiologically relevant conditions.
引用
收藏
页码:1009 / +
页数:19
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