Department of Neuropharmacology, Graduate School of Medicine and Engineering, University of Yamanashi, Yamanashi 409-3898, Japan.
Glia. 2013 Jan;61(1):47-54. doi: 10.1002/glia.22358. Epub 2012 Jun 1.
Microglia are sensitive to environmental changes and are immediately transformed into several phenotypes. For such dynamic "modal shifts", purinergic receptors have central roles. When microglia sense ATP/ADP leaked from injured cells by P2Y(12) receptors, they are transformed into a moving phenotype, showing process extension and migration toward the injured sites. Microglia upregulate adenosine A(2A) receptors, by which they retract the processes showing an amoeboid-shaped, activated phenotype. Microglia also upregulate P2Y(6) receptors, and if they meet UDP leaked from dead cells, microglia start to engulf and eat the dead cells as a phagocytic phenotype. The P2Y(12) receptor-mediated responses are modulated by other P2 or P1 receptors. In contrast, the P2Y(6) receptor-mediated responses were not influenced by P2Y(12) receptors and vice versa. Microglia appear to use purinergic signals either cooperatively or distinctively to cause their modal shifts.
小胶质细胞对环境变化敏感,并立即转变为几种表型。对于这种动态的“模态转换”,嘌呤能受体起着核心作用。当小胶质细胞通过 P2Y(12)受体感知到损伤细胞漏出的 ATP/ADP 时,它们会转变为移动表型,表现为向损伤部位延伸和迁移。小胶质细胞上调嘌呤能受体 A(2A),通过这种受体,它们缩回呈现出阿米巴样、激活表型的突起。小胶质细胞还上调 P2Y(6)受体,如果它们遇到从死亡细胞漏出的 UDP,小胶质细胞就会开始吞噬和吃掉死亡细胞,表现出吞噬表型。P2Y(12)受体介导的反应受到其他 P2 或 P1 受体的调节。相比之下,P2Y(6)受体介导的反应不受 P2Y(12)受体的影响,反之亦然。小胶质细胞似乎协同或独立地利用嘌呤能信号来引起它们的模态转换。