Molecular mechanisms of glial swelling in vitro.

O Kempski, F Staub, F von Rosen, M Zimmer, A Neu, A Baethmann
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引用次数: 59

Abstract

The pathophysiological chain of events occurring during cerebral ischemia is still poorly understood on a molecular level. Therefore, an in vitro model to study glial swelling mechanisms, using C6 glial cells under controlled extracellular conditions, has been established. Flow cytometry serves to determine even small cell volume changes. In this report, the effects of anoxia and acidosis on glial swelling are summarized. Anoxia alone, or in combination with iodoacetate to inhibit anaerobic glycolysis, did not cause an increase of glial volume for up to 2 h. Acidification of the incubation medium below pH 6.8, on the other hand, was immediately followed by cell swelling to 115% of normal. Amiloride or the absence of bicarbonate and Na+ in the medium significantly reduced glial swelling. The data support the contention that swelling results from an activation of the Na+/H+-antiporter to control intracellular pH. It is suggested that swelling in an ischemic penumbra is promoted by this mechanism. Therapeutic approaches to control cerebral pH might be useful to protect brain tissue in cerebral ischemia.

胶质细胞体外肿胀的分子机制。
脑缺血过程中发生的病理生理链在分子水平上仍然知之甚少。因此,我们建立了一个体外模型,在受控的细胞外条件下使用C6胶质细胞来研究胶质细胞肿胀机制。流式细胞术甚至可以测定很小的细胞体积变化。本文就缺氧和酸中毒对神经胶质肿胀的影响作一综述。单独缺氧,或与碘乙酸联合抑制厌氧糖酵解,在2小时内不会引起胶质体积的增加。另一方面,在pH低于6.8的孵育培养基酸化后,细胞立即肿胀到正常水平的115%。阿米洛利或培养基中不含碳酸氢盐和Na+可显著降低胶质细胞肿胀。这些数据支持这样的观点,即肿胀是由Na+/H+-反转运蛋白激活来控制细胞内ph引起的。这表明,缺血半暗带的肿胀是由这种机制促进的。控制脑pH值的治疗方法可能有助于脑缺血脑组织的保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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