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首页> 外文期刊>The Journal of biological chemistry >Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity
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Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity

机译:KCNJ16的遗传失活认为Kir5.1作为神经元PCO2 / pH敏感性的重要决定因素

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The molecular identity of ion channels which confer PCO2/pH sensitivity in the brain is unclear. Heteromeric Kir4.1/Kir5.1 channels are highly sensitive to inhibition by intracellular pH and are widely expressed in several brainstem nuclei involved in cardiorespiratory control, including the locus coeruleus. This has therefore led to a proposed role for these channels in neuronal CO2 chemosensitivity. To examine this, we generated mutant mice lacking the Kir5.1 (Kcnj16) gene. We show that although locus coeruleus neurons from Kcnj16(+/+) mice rapidly respond to cytoplasmic alkalinization and acidification, those from Kcnj16(?/?) mice display a dramatically reduced and delayed response. These results identify Kir5.1 as an important determinant of PCO2/pH sensitivity in locus coeruleus neurons and suggest that Kir5.1 may be involved in the response to hypercapnic acidosis.
机译:在大脑中赋予PCO2 / pH敏感性的离子通道的分子标识尚不清楚。异聚kir4.1 / kir5.1通道对细胞内pH的抑制非常敏感,并且广泛表达涉及心肺控制的几种脑干细胞核,包括基因座Coeruleus。因此,这导致了这些通道在神经元二氧化碳化学敏感性中的拟议作用。为了检查这一点,我们产生缺乏KIR5.1(KCNJ16)基因的突变小鼠。我们表明,虽然来自KCNJ16(+ / +)小鼠的遗迹Coeruleus神经元快速响应细胞质碱化和酸化,来自KCNJ16(β/β)小鼠的小鼠显示出显着减少和延迟的响应。这些结果将Kir5.1鉴定为基因座Coeruleus神经元的PCO2 / pH敏感性的重要决定因素,并表明Kir5.1可以参与对高脂合酸中毒的反应。

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