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小胶质细胞通过UDP-P2Y6受体系统对感染细菌的昼夜动态反应。

Diurnal dynamic behavior of microglia in response to infected bacteria through the UDP-P2Y6 receptor system.

作者信息

Takayama Fumiko, Hayashi Yoshinori, Wu Zhou, Liu Yicong, Nakanishi Hiroshi

机构信息

Department of Aging Science and Pharmacology, Faculty of Dental Science, Kyushu University, Fukuoka 812-8582, Japan.

JSPS Research Fellow, 5-3-1 Kojimachi, Chiyoda-ku, Tokyo 102-0083, Japan.

出版信息

Sci Rep. 2016 Jul 21;6:30006. doi: 10.1038/srep30006.

Abstract

It has long been believed that microglia morphologically transform into the activated state by retracting their long processes and consuming pathogens when bacteria infect into the brain parenchyma. In the present study, however, we showed for the first time that murine cortical microglia extend their processes towards focally injected Porphyromonas gingivalis. This P. gingivalis-induced microglial process extension was significantly increased during the light (sleeping) phase than the dark (waking) phase. In contrast, focally injected ATP-induced microglial process extension was significantly increased during the dark phase than the light phase. Furthermore, in contrast to the P2Y12 receptor-mediated mechanism of ATP-induced microglial process extension, the P. gingivalis-mediated microglial process extension was mediated by P2Y6 receptors. The infection of bacteria such as P. gingivalis to the brain parenchyma may induce the secretion of UDP from microglia at the site of infection, which in turn induces the process extension of the neighboring microglia.

摘要

长期以来,人们一直认为,当细菌侵入脑实质时,小胶质细胞会通过缩回其长突起并吞噬病原体,在形态上转变为激活状态。然而,在本研究中,我们首次表明,小鼠皮质小胶质细胞会将其突起伸向局部注射的牙龈卟啉单胞菌。与黑暗(清醒)阶段相比,在光照(睡眠)阶段,这种牙龈卟啉单胞菌诱导的小胶质细胞突起延伸显著增加。相反,与光照阶段相比,在黑暗阶段,局部注射ATP诱导的小胶质细胞突起延伸显著增加。此外,与ATP诱导的小胶质细胞突起延伸的P2Y12受体介导机制相反,牙龈卟啉单胞菌介导的小胶质细胞突起延伸由P2Y6受体介导。牙龈卟啉单胞菌等细菌感染脑实质可能会诱导感染部位的小胶质细胞分泌UDP,进而诱导邻近小胶质细胞的突起延伸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5d7/4956748/96d9822b7cab/srep30006-f1.jpg

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