Werner P, Seward E P, Buell G N, North R A
Geneva Biomedical Research Institute, Glaxo Wellcome Research and Development, Switzerland.
Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15485-90. doi: 10.1073/pnas.93.26.15485.
ATP-gated ion channels (P2X receptors) are abundantly expressed in both neuronal and nonneuronal tissues, where they can serve as postsynaptic receptors. The response to ATP shows marked desensitization in some tissues but not others. Currents induced by ATP in Xenopus oocytes expressing cloned P2X1 (or P2X3) receptor had strong desensitization, whereas currents in cells expressing P2X2 receptors desensitized relatively little (90% vs. 14% decline of current in a 10-s application). In chimeric receptors, substitution into the P2X1 receptor of either one of two 34-residue segments from the P2X2 receptor removed the desensitization; these segments included the first or the second hydrophobic domain. In contrast, desensitization was introduced into the P2X2 receptor only by providing both these segments of the P2X1 (or P2X3) receptor. This suggests that desensitization requires interaction between the two hydrophobic domains of the receptor, and supports the view that these are membrane-spanning segments.
ATP门控离子通道(P2X受体)在神经元和非神经元组织中均有大量表达,在这些组织中它们可作为突触后受体。对ATP的反应在某些组织中表现出明显的脱敏现象,而在其他组织中则不然。在表达克隆的P2X1(或P2X3)受体的非洲爪蟾卵母细胞中,ATP诱导的电流有强烈的脱敏现象,而在表达P2X2受体的细胞中,电流的脱敏相对较少(在施加10秒时电流下降90%对14%)。在嵌合受体中,将P2X2受体的两个34个残基片段中的任何一个替换到P2X1受体中,均可消除脱敏现象;这些片段包括第一个或第二个疏水结构域。相反,只有通过提供P2X1(或P2X3)受体的这两个片段,才会将脱敏现象引入P2X2受体。这表明脱敏需要受体的两个疏水结构域之间相互作用,并支持了这些结构域是跨膜片段的观点。