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大脑和背根神经节细胞中酸敏感离子通道的一个调节亚基。

A modulatory subunit of acid sensing ion channels in brain and dorsal root ganglion cells.

作者信息

Lingueglia E, de Weille J R, Bassilana F, Heurteaux C, Sakai H, Waldmann R, Lazdunski M

机构信息

Institut de Pharmacologie Moléculaire et Cellulaire, CNRS-UPR 411, 660 route des Lucioles, Sophia Antipolis, 06560 Valbonne, France.

出版信息

J Biol Chem. 1997 Nov 21;272(47):29778-83. doi: 10.1074/jbc.272.47.29778.

Abstract

MDEG1 is a cation channel expressed in brain that belongs to the degenerin/epithelial Na+ channel superfamily. It is activated by the same mutations which cause neurodegeneration in Caenorhabditis elegans if present in the degenerins DEG-1, MEC-4, and MEC-10. MDEG1 shares 67% sequence identity with the recently cloned proton-gated cation channel ASIC (acid sensing ion channel), a new member of the family which is present in brain and in sensory neurons. We have now identified MDEG1 as a proton-gated channel with properties different from those of ASIC. MDEG1 requires more acidic pH values for activation and has slower inactivation kinetics. In addition, we have cloned from mouse and rat brain a splice variant form of the MDEG1 channel which differs in the first 236 amino acids, including the first transmembrane region. This new membrane protein, which has been called MDEG2, is expressed in both brain and sensory neurons. MDEG2 is activated neither by mutations that bring neurodegeneration once introduced in C. elegans degenerins nor by low pH. However, it can associate both with MDEG1 and another recently cloned H+-activated channel DRASIC to form heteropolymers which display different kinetics, pH dependences, and ion selectivities. Of particular interest is the subunit combination specific for sensory neurons, MDEG2/DRASIC. In response to a drop in pH, it gives rise to a biphasic current with a sustained current which discriminates poorly between Na+ and K+, like the native H+-gated current recorded in dorsal root ganglion cells. This sustained current is thought to be required for the tonic sensation of pain caused by acids.

摘要

MDEG1是一种在大脑中表达的阳离子通道,属于退化素/上皮钠通道超家族。如果在退化素DEG-1、MEC-4和MEC-10中存在导致秀丽隐杆线虫神经退行性变的相同突变,MDEG1就会被激活。MDEG1与最近克隆的质子门控阳离子通道ASIC(酸敏感离子通道)具有67%的序列同一性,ASIC是该家族的一个新成员,存在于大脑和感觉神经元中。我们现已确定MDEG1是一种质子门控通道,其特性与ASIC不同。MDEG1需要更酸性的pH值来激活,并且失活动力学较慢。此外,我们从小鼠和大鼠大脑中克隆出了MDEG1通道的一种剪接变体形式,其前236个氨基酸不同,包括第一个跨膜区域。这种新的膜蛋白被称为MDEG2,在大脑和感觉神经元中均有表达。MDEG2既不会因引入秀丽隐杆线虫退化素中会导致神经退行性变的突变而被激活,也不会因低pH值而被激活。然而,它可以与MDEG1以及另一种最近克隆的H+激活通道DRASIC结合形成异源聚合物,这些异源聚合物表现出不同的动力学、pH依赖性和离子选择性。特别有趣的是感觉神经元特有的亚基组合MDEG2/DRASIC。响应pH值下降时,它会产生一种双相电流,其中持续电流对Na+和K+的区分能力较差,就像在背根神经节细胞中记录到的天然H+门控电流一样。这种持续电流被认为是酸引起的持续性疼痛感觉所必需的。

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