摘要
Protease-activated受体(PARs)是最新的的g蛋白耦合的受体(GPCRs)的激活需要乳沟的n端丝氨酸蛋白酶。然而,最近的证据表明,替代路线的激活也发生,PARs信号通过多种途径,途径激活催化剂-依赖。鉴于我们增加票面价值函数的理解都在生理和病理生理条件下,一个方面是保持不变的PAR2和炎症之间的联系。PAR2表达在免疫细胞的先天和适应性免疫系统已被证明在几个外围炎症中发挥作用的条件。PAR2同样表达了对星形胶质细胞和小胶质细胞在中枢神经系统,激活保护或损害中枢神经系统功能根据条件或疾病状态调查。有明确的相似性函数PAR2中枢神经系统免疫细胞和神经胶质细胞,我们回顾了他们的角色在这两个系统。我们建议最新的PAR2调节器的最新发展,包括那些显示偏差信号,将进一步增加我们的理解PAR2功能和潜在的发展提出了治疗中枢神经系统疾病,炎症扮演一个角色。
关键词: PAR2. 中枢神经系统障碍. 神经胶质. 免疫细胞. 炎症. 神经元
图形摘要
Current Drug Targets
Title:Protease-Activated Receptor 2: Are Common Functions in Glial and Immune Cells Linked to Inflammation-Related CNS Disorders?
Volume: 17 Issue: 16
Author(s): Trevor J. Bushell, Margaret R. Cunningham, Kathryn A. McIntosh, Serge Moudio, Robin Plevin
Affiliation:
关键词: PAR2. 中枢神经系统障碍. 神经胶质. 免疫细胞. 炎症. 神经元
摘要: Protease-activated receptors (PARs) are a novel family of G-protein coupled receptors (GPCRs) whose activation requires the cleavage of the N-terminus by a serine protease. However, recent evidence reveals that alternative routes of activation also occur, that PARs signal via multiple pathways and that pathway activation is activator- dependent. Given our increased understanding of PAR function both under physiological and pathophysiological conditions, one aspect that has remained constant is the link between PAR2 and inflammation. PAR2 is expressed in immune cells of both the innate and adaptive immune system and has been shown to play a role in several peripheral inflammatory conditions. PAR2 is similarly expressed on astrocytes and microglia within the CNS and its activation is either protective or detrimental to CNS function depending on the conditions or disease state investigated. With a clear similarity between the function of PAR2 on both immune cells and CNS glial cells, here we have reviewed their roles in both these systems. We suggest that the recent development of novel PAR2 modulators, including those that show biased signalling, will further increase our understanding of PAR2 function and the development of potential therapeutics for CNS disorders in which inflammation is proposed to play a role.
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Cite this article as:
Trevor J. Bushell, Margaret R. Cunningham, Kathryn A. McIntosh, Serge Moudio, Robin Plevin , Protease-Activated Receptor 2: Are Common Functions in Glial and Immune Cells Linked to Inflammation-Related CNS Disorders?, Current Drug Targets 2016; 17 (16) . https://dx.doi.org/10.2174/1389450117666151209115232
DOI https://dx.doi.org/10.2174/1389450117666151209115232 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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