Hypoxia-induced changes of rat skeletal muscle were investigated by two-dimensional difference ingel electrophoresis (2D-DIGE) and mass spectrometry. The results indicated that proteins involved in the TCA cycle, ATP production, and electron transport are down-regulated, whereas glycolytic enzymes and deaminases involved in ATP and AMP production were up-regulated. Up-regulation of the hypoxia markers hypoxia inducible factor 1 (HIF-1α) and pyruvate dehydrogenase kinase 1 (PDK1) was also observed, suggesting that in vivo adaptation to hypoxia requires an active metabolic switch. The kinase protein, mammalian target of rapamycin (mTOR), which has been implicated in the regulation of protein synthesis in hypoxia, appears unchanged, suggesting that its activity, in this system, is not controlled by oxygen partial pressure.

Metabolic modulation induced by chronic hypoxia in rats using a comparative proteomic analysis of skeletal muscle tissue / S. De Palma, M. Ripamonti, A. Viganò, M. Moriggi, D. Capitanio, M. Samaja, G. Milano, P. Cerretelli, R. Wait, C. Gelfi, D. Capitanio. - In: JOURNAL OF PROTEOME RESEARCH. - ISSN 1535-3893. - 6:5(2007), pp. 1974-1984.

Metabolic modulation induced by chronic hypoxia in rats using a comparative proteomic analysis of skeletal muscle tissue

M. Moriggi;D. Capitanio;M. Samaja;P. Cerretelli;C. Gelfi;D. Capitanio
2007

Abstract

Hypoxia-induced changes of rat skeletal muscle were investigated by two-dimensional difference ingel electrophoresis (2D-DIGE) and mass spectrometry. The results indicated that proteins involved in the TCA cycle, ATP production, and electron transport are down-regulated, whereas glycolytic enzymes and deaminases involved in ATP and AMP production were up-regulated. Up-regulation of the hypoxia markers hypoxia inducible factor 1 (HIF-1α) and pyruvate dehydrogenase kinase 1 (PDK1) was also observed, suggesting that in vivo adaptation to hypoxia requires an active metabolic switch. The kinase protein, mammalian target of rapamycin (mTOR), which has been implicated in the regulation of protein synthesis in hypoxia, appears unchanged, suggesting that its activity, in this system, is not controlled by oxygen partial pressure.
2D-DIGE; Hypoxia; Mass spectrometry; Skeletal muscle
Settore BIO/10 - Biochimica
Settore BIO/09 - Fisiologia
Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
2007
http://pubs.acs.org/cgi-bin/article.cgi/jprobs/2007/6/i05/pdf/pr060614o.pdf
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/35242
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