A central role of connexin 43 in hypoxic preconditioning

被引:145
作者
Lin, Jane H. -C. [1 ,2 ]
Lou, Nanhong [3 ]
Kang, Ning
Takano, Takahiro [3 ]
Hu, Furong [1 ,2 ]
Han, Xiaoning [3 ]
Xu, Qiwu [3 ]
Lovatt, Ditte [3 ]
Torres, Arnulfo [3 ]
Willecke, Klaus [4 ]
Yang, Jay [5 ]
Kang, Jian
Nedergaard, Maiken
机构
[1] New York Med Coll, Dept Pathol, Valhalla, NY 10595 USA
[2] New York Med Coll, Dept Cell Biol, Valhalla, NY 10595 USA
[3] Univ Rochester, Med Ctr, Dept Neurosurg, Div Glial Dis & Therapeut, Rochester, NY 14642 USA
[4] Univ Bonn, Inst Genet, D-53117 Bonn, Germany
[5] Columbia Univ, Dept Anesthesiol, Div Neurobiol Res Anesthesia, New York, NY 10032 USA
关键词
gap junction; astrocytes; hemichannels; stroke; adenosine; GFAP;
D O I
10.1523/JNEUROSCI.3827-07.2008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:681 / 695
页数:15
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