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连接蛋白43在缺氧预处理中的核心作用。

A central role of connexin 43 in hypoxic preconditioning.

作者信息

Lin Jane H-C, Lou Nanhong, Kang Ning, Takano Takahiro, Hu Furong, Han Xiaoning, Xu Qiwu, Lovatt Ditte, Torres Arnulfo, Willecke Klaus, Yang Jay, Kang Jian, Nedergaard Maiken

机构信息

Department of Pathology, New York Medical College, Valhalla, New York 10595, USA.

出版信息

J Neurosci. 2008 Jan 16;28(3):681-95. doi: 10.1523/JNEUROSCI.3827-07.2008.

Abstract

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.

摘要

预处理是一种内源性机制,即非致死性暴露可增加细胞对随后额外严重损伤的抵抗力。我们在此表明,连接蛋白43(Cx43)在预处理所提供的保护中起关键作用。Cx43基因敲除小鼠对缺氧预处理不敏感,而野生型同窝小鼠在大脑中动脉闭塞后梗死体积显著减小。在培养物中,Cx43缺陷细胞仅在Cx43外源表达后才对预处理产生反应,并且保护作用会被小干扰RNA或通道阻滞剂减弱。我们的观察结果表明,预处理减少了Cx43的降解,导致质膜Cx43半通道数量显著增加。因此,ATP通过半通道流出导致其分解代谢产物腺苷(一种有效的神经保护剂)积累。因此,Cx43的适应性调节可通过腺苷介导的细胞抵抗力升高来抵消环境应激。

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A central role of connexin 43 in hypoxic preconditioning.连接蛋白43在缺氧预处理中的核心作用。
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