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A central role of connexin 43 in hypoxic preconditioning

期刊

JOURNAL OF NEUROSCIENCE
卷 28, 期 3, 页码 681-695

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.3827-07.2008

关键词

gap junction; astrocytes; hemichannels; stroke; adenosine; GFAP

资金

  1. NINDS NIH HHS [R01 NS056188, NS50315, P01 NS050315] Funding Source: Medline

向作者/读者索取更多资源

Preconditioning is an endogenous mechanism in which a nonlethal exposure increases cellular resistance to subsequent additional severe injury. Here we show that connexin 43 (Cx43) plays a key role in protection afforded by preconditioning. Cx43 null mice were insensitive to hypoxic preconditioning, whereas wild-type littermate mice exhibited a significant reduction in infarct volume after occlusion of the middle cerebral artery. In cultures, Cx43-deficient cells responded to preconditioning only after exogenous expression of Cx43, and protection was attenuated by small interference RNA or by channel blockers. Our observations indicate that preconditioning reduced degradation of Cx43, resulting in a marked increase in the number of plasma membrane Cx43 hemichannels. Consequently, efflux of ATP through hemichannels led to accumulation of its catabolic product adenosine, a potent neuroprotective agent. Thus, adaptive modulation of Cx43 can offset environmental stress by adenosine-mediated elevation of cellular resistance.

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