[嘌呤能P2X家族和P2X7亚型的具体特征]。

Ceskoslovenska fysiologie Pub Date : 2013-01-01
M Jindrichová, H Zemková
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引用次数: 0

摘要

嘌呤能P2X受体(P2XR)由细胞外腺苷5'-三磷酸(ATP)激活,是一种特殊类型的配体门控离子通道。它们形成功能性三聚体或异构体,在受体激活后具有非选择性阳离子渗透性。P2X受体广泛表达于可兴奋组织和不可兴奋组织中,参与血小板聚集、平滑肌收缩、免疫反应、细胞增殖和凋亡、神经传递等多种生理和病理生理过程。在哺乳动物中,已鉴定出7个P2X亚基(P2X1-P2X7)。它们主要在atp诱导反应的分布、药理学特征和动力学上有所不同。P2X7亚型是P2X家族中最特异的亚型,与其他P2X亚型有很大不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Purinergic P2X family and specific features of the P2X7 subtype].

Purinergic P2X receptors (P2XR), activated by extracellular adenosine 5'-triphosphate (ATP), represent a specific type of ligand-gated ion channels. They form functional trimeric homomers or heteromers which are nonselectively cation-permeable after receptor activation. P2X receptors are widely expressed in excitable and nonexcitable tissues and are involved in many physiological and pathophysiological processes such as platelet aggregation, contraction of smooth muscle, immune responses, cell proliferation and apoptosis or neurotransmission. In mammals, seven P2X subunits (P2X1-P2X7) have been identified. They differ mainly in distribution, pharmacological profile and kinetics of ATP-induced responses. The subtype P2X7 is the most specific in the P2X family and widely differs from other P2X subtypes.

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