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嘌呤能受体和通道在垂体中的信号转导。

Signaling by purinergic receptors and channels in the pituitary gland.

机构信息

Section on Cellular Signaling, Program in Developmental Neuroscience, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-4510, USA.

出版信息

Mol Cell Endocrinol. 2010 Jan 27;314(2):184-91. doi: 10.1016/j.mce.2009.05.008. Epub 2009 May 23.

Abstract

Adenosine 5'-triphosphate is frequently released by cells and acts as an agonist for G protein-coupled P2Y receptors and ligand-gated P2X cationic channels in numerous tissues. The breakdown of ATP by ectonucleotidases not only terminates its extracellular messenger functions, but also provides a pathway for the generation of two additional agonists: adenosine 5'-diphosphate, acting via some P2Y receptors, and adenosine, a native agonist for G protein-coupled adenosine receptors. In the pituitary gland, adenosine 5'-triphosphate is released from the endings of magnocellular hypothalamic neurons and by anterior pituitary cells through pathway(s) that are still not well characterized. This gland also expresses several members of each family of purinergic receptors. P2X and adenosine receptors are co-expressed in the somata and nerve terminals of vasopressin-releasing neurons as well as in some secretory pituitary cells. P2X receptors stimulate electrical activity and modulate InsP(3)-dependent calcium release from intracellular stores, whereas adenosine receptors terminate electrical activity. Calcium-mobilizing P2Y receptors are expressed in pituicytes, folliculo-stellate cells and some secretory cells of the anterior pituitary.

摘要

三磷酸腺苷经常由细胞释放,并作为许多组织中 G 蛋白偶联 P2Y 受体和配体门控 P2X 阳离子通道的激动剂发挥作用。核苷酸酶对 ATP 的分解不仅终止其细胞外信使功能,而且还为另外两种激动剂的产生提供了途径:二磷酸腺苷,通过一些 P2Y 受体起作用,以及腺苷,一种 G 蛋白偶联腺苷受体的天然激动剂。在垂体中,三磷酸腺苷从大细胞下丘脑神经元的末梢以及通过前垂体细胞释放,其途径尚未很好地描述。该腺体还表达每种嘌呤能受体家族的几个成员。P2X 和腺苷受体在促血管加压素释放神经元的体和神经末梢以及一些分泌性垂体细胞中共表达。P2X 受体刺激电活动并调节细胞内储存的 InsP(3)依赖性钙释放,而腺苷受体终止电活动。动员钙的 P2Y 受体表达在垂体细胞、滤泡星状细胞和前垂体的一些分泌细胞中。

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