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Am J Physiol Heart Circ Physiol 292: H751-H757, 2007. First published November 10, 2006; doi:10.1152/ajpheart.01016.2006
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Oxygen Sensing: Life and Death of a Cell

Acute intermittent hypoxia activates myocardial cell survival signaling

Ah-Mee Park, Hiroko Nagase, Shilpashree Vinod Kumar, and Yuichiro J. Suzuki

Department of Pharmacology, Georgetown University Medical Center, Washington, DC

Submitted 16 September 2006 ; accepted in final form 6 November 2006

Intermittent hypoxia (IH) with repeated episodes of hypoxia-normoxia cycle has been shown to exert preconditioning-like cardioprotective effects. To understand the mechanism of these events, we investigated the changes in cardiac gene expression in response to acute IH. Mice were subjected to five cycles of 2 min of 10% O2 plus 2 min of 21% O2. RNA was isolated, and gene array analysis was performed. Results show that the expression of antiapoptotic genes, such as Bcl-2 and Bcl-xL, were increased after acute IH. GATA-4 regulates transcription of these genes, and, consistently, GATA-4 activity was increased by acute IH. Although the phosphorylation of GATA-4 has been shown to regulate its activity, no changes in GATA-4 phosphorylation status by acute IH were noted. Gene transcription of gata4 was increased by acute IH, and this might be responsible for the enhanced GATA activity. To understand the mechanism of acute IH activation of gata4 gene transcription, we identified a promoter region of the mouse gata4 gene that is 1,000 bp immediately upstream from the transcriptional start site. In cardiac muscle cells, truncation of 1,000 to 250 bp did not alter the transcriptional activity, suggesting that the proximal 250-bp region contains important transcriptional regulatory sites. We further found that acute IH activates factors which bind to the proximal 100-bp region. Thus acute IH activates not yet identified factors that bind to the proximal 100-bp region of the gata4 promoter and, in turn, increases gata4 gene transcription, leading to enhanced expression of Bcl-2 and Bcl-xL.

Bcl; cardioprotection; GATA-4; heart; promoter



Address for reprint requests and other correspondence: Y. J. Suzuki, Dept. of Pharmacology, Georgetown Univ. Medical Center, NW403 Medical-Dental Bldg., 3900 Reservoir Rd. NW, Washington, DC 20057 (e-mail: ys82{at}georgetown.edu)




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A.-M. Park and Y. J. Suzuki
Effects of intermittent hypoxia on oxidative stress-induced myocardial damage in mice
J Appl Physiol, May 1, 2007; 102(5): 1806 - 1814.
[Abstract] [Full Text] [PDF]




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