Chen Z P, Levy A, Lightman S L
Department of Medicine, University of Bristol, Bristol Royal Infirmary, UK.
J Neuroendocrinol. 1995 Feb;7(2):83-96. doi: 10.1111/j.1365-2826.1995.tb00671.x.
There is now wide acceptance that ATP and other nucleotides are ubiquitous extracellular chemical messengers. ATP and diadenosine polyphosphates can be released from synaptosomes. They act on a large and diverse family of P2 purinoceptors, four of which have been cloned. This receptor family can be divided into two distinct classes: ligand-gated ion channels for P2X receptors and G protein-coupled receptors for P2Y, P2U, P2T and P2D receptors. The P2Y, P2U and P2D receptors have a fairly wide tissue distribution, while the P2X receptor is mainly found in neurons and muscles and the P2T and P2Z receptors confined to platelets and immune cells, respectively. Inositol phosphate and calcium signalling appear to be the predominant mechanisms for transducing the G-protein linked P2 receptor signals. Multiple P2 receptors are expressed by neurons and glia in the CNS and also in neuroendocrine cells. ATP and other nucleotides may therefore have important roles not only as a neurotransmitter but also as a neuroendocrine regulatory messenger.
目前,ATP和其他核苷酸作为普遍存在的细胞外化学信使已被广泛接受。ATP和多磷酸二腺苷可以从突触体释放。它们作用于一个庞大且多样的P2嘌呤受体家族,其中四种已被克隆。这个受体家族可分为两个不同的类别:P2X受体的配体门控离子通道和P2Y、P2U、P2T及P2D受体的G蛋白偶联受体。P2Y、P2U和P2D受体具有相当广泛的组织分布,而P2X受体主要存在于神经元和肌肉中,P2T和P2Z受体则分别局限于血小板和免疫细胞。肌醇磷酸和钙信号似乎是转导G蛋白偶联P2受体信号的主要机制。中枢神经系统中的神经元、胶质细胞以及神经内分泌细胞均表达多种P2受体。因此,ATP和其他核苷酸不仅可能作为神经递质,还可能作为神经内分泌调节信使发挥重要作用。