期刊文献+

P2X7受体在胞内病原体感染中的研究进展

Research progress regarding the P2X7 receptor in intracellular pathogen infection
下载PDF
导出
摘要 P2X7受体属于ATP激活的非选择性阳离子通道型受体,其在人体分布广泛,参与调控机体的多种生理过程。当细菌、病毒或寄生虫攻击免疫系统时,ATP从宿主细胞释放,在细胞外作为危险信号,激活P2X7受体,参与免疫应答和炎症反应,如活性氧的产生、促进溶酶体吞噬作用、释放细胞因子和趋化因子,介导NLRP3炎性小体的形成,促进IL-1β成熟和释放等。近年来,基于P2X7受体基因靶向敲除动物模型的成功构建和特异性P2X7受体拮抗剂的研发,该受体有望成为治疗胞内病原体感染的新靶点。本文以P2X7受体特征、分布,在细菌、病毒、寄生虫感染中的研究进展作一综述,并探讨该受体作为感染性疾病治疗靶点的潜力。 The P2X7 receptor is a non-selective cationic channel receptor activated by ATP.It is widely distributed in the human body and participates in the regulation of various physiological processes.When bacteria,viruses,or parasites attack the immune system,ATP is released from host cells during infection and acts as a danger signal in the extracellular space by activating the P2X7 receptor,which is involved in the immune response and inflammation.Its functions include the production of reactive oxygen,phagolysosomal fusion,release of cytokines and chemokines,and participation in mediating the formation of NLRP3 inflammasomes and the maturation and release of IL-1β.Based on the recent successful construction of animal models of targeted knockout of the P2X7 receptor gene and the development of specific P2X7 receptor antagonists,this receptor is expected to become a potential target for the treatment of intracellular pathogen infection.This review will focus on the characteristics and distribution of the P2X7 receptor,as well as the progress made in research on the P2X7 receptor in bacterial,viral,and parasitic infections,hoping to provide a new insight into the potential of this receptor as a therapeutic target for infectious diseases.
作者 贺樟平 陈列松 吴移谋 HE Zhang-ping;CHEN Lie-song;WU Yi-mou(Institute of Pathogenic Biology,University of South China,Hengyang 421001,China)
出处 《中国人兽共患病学报》 CAS CSCD 北大核心 2021年第11期1037-1043,共7页 Chinese Journal of Zoonoses
基金 国家自然科学基金(No.31872643)。
关键词 P2X7受体 ATP 胞内病原体 感染 P2X7 receptors ATP intracellular pathogen infection
  • 相关文献

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部