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G 蛋白偶联受体在风湿病学中的作用。

G protein-coupled receptors in rheumatology.

机构信息

Department of Internal Medicine and Rheumatology, Justus-Liebig University of Giessen, Rheumatology and Clinical Immunology, Kerckhoff Klinik, GmbH, Benekestrasse 2-8, Bad Nauheim D-61231, Germany.

出版信息

Nat Rev Rheumatol. 2014 Jul;10(7):429-36. doi: 10.1038/nrrheum.2014.62. Epub 2014 May 6.

Abstract

G protein-coupled receptors (GPCRs) are transmembrane receptor proteins that allow the transfer of signals across the cell membrane. In addition to their physiological role, GPCRs are involved in many pathophysiological processes including pathways relevant in rheumatoid arthritis (RA), osteoarthritis (OA) and psoriatic arthritis. Two-thirds of all currently available drugs target GPCRs directly or indirectly. However, the detailed mechanism of GPCR signalling is still unclear. Selective modification of GPCR-dependent signalling cascades to inhibit disease progression in rheumatic diseases is now being investigated. One approach is to use antibodies against ligands activating GPCRs. However, several GPCRs are known to be activated by only one ligand. In this case, targeting the receptor itself is a promising approach. So far, more information is available on GPCR action in RA as compared with OA, and even less information is available for other rheumatic diseases. Additional research on the role of GPCRs involved in the pathophysiology of rheumatic diseases is required to develop specific therapeutic approaches.

摘要

G 蛋白偶联受体(GPCRs)是一种跨膜受体蛋白,能够在细胞膜间传递信号。除了发挥生理作用外,GPCR 还参与多种病理生理过程,包括与类风湿关节炎(RA)、骨关节炎(OA)和银屑病关节炎相关的途径。目前约有三分之二的可用药物直接或间接地靶向 GPCR。然而,GPCR 信号转导的详细机制仍不清楚。目前正在研究选择性修饰 GPCR 依赖性信号级联反应,以抑制风湿性疾病的进展。一种方法是使用针对激活 GPCR 的配体的抗体。然而,已知一些 GPCR 仅被一种配体激活。在这种情况下,靶向受体本身是一种很有前途的方法。迄今为止,与 OA 相比,关于 RA 中 GPCR 作用的信息更多,而对于其他风湿性疾病的信息则更少。需要进一步研究风湿性疾病病理生理学中涉及的 GPCR 作用,以开发特定的治疗方法。

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