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感觉神经元通过与线粒体相关的一氧化氮产生来对缺氧作出反应。

Sensory neurons respond to hypoxia with NO production associated with mitochondria.

作者信息

Henrich Michael, Hoffmann Karin, König Peter, Gruss Marco, Fischbach Tamara, Gödecke Axel, Hempelmann Gunter, Kummer Wolfgang

机构信息

Department of Anaesthesiology and Intensive Care, Justus-Liebig-University, D-35385 Giessen, Germany.

出版信息

Mol Cell Neurosci. 2002 Jun;20(2):307-22. doi: 10.1006/mcne.2002.1111.

Abstract

Oxygen is pivotal for mammalian cell function, and recent studies suggest an involvement of NO in cellular adaptation to low oxygen supply. Here, we report that endothelial NO-synthase is ubiquitously expressed in rat and mice sensory neurons, and is targeted to juxtamitochondrial compartments of the ER. There it is activated in response to hypoxia while generation of reactive oxygen species remains unaltered. Developing a technique for ultrastructural localization of an NO-sensitive indicator allowed to identify the inner mitochondrial membrane as the target of NO under hypoxia. The demonstrated hypoxic stimulation of endothelial NOS in sensory neurons shall contribute to resistance against hypoxia, since NO promotes cellular survival by interfering with mitochondrial function.

摘要

氧气对哺乳动物细胞功能至关重要,最近的研究表明一氧化氮参与细胞对低氧供应的适应。在此,我们报告内皮型一氧化氮合酶在大鼠和小鼠感觉神经元中普遍表达,并定位于内质网的近线粒体区室。在那里,它在缺氧时被激活,而活性氧的产生保持不变。开发一种用于一氧化氮敏感指示剂超微结构定位的技术,使得能够确定线粒体内膜是缺氧时一氧化氮的作用靶点。感觉神经元中内皮型一氧化氮合酶的缺氧刺激作用已得到证实,这有助于抵抗缺氧,因为一氧化氮通过干扰线粒体功能促进细胞存活。

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