小胶质细胞CD39将ATP酶降解为腺苷调节神经血管偶联和脑代谢供应。

IF 3 4区医学 Q2 NEUROSCIENCES

Purinergic Signalling Pub Date : 2025-06-20 DOI:10.1007/s11302-025-10102-w

Jing Guo, Yong Tang, Peter Illes

引用次数: 0

摘要

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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The enzymatic degradation of ATP to adenosine by microglial CD39 regulates neurovascular coupling and metabolic supply to the brain.

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来源期刊

Purinergic Signalling 医学-神经科学

CiteScore

6.60

自引率

17.10%

发文量

审稿时长

6-12 weeks

期刊介绍： Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.