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CXCR6/CXCL16 轴在自身免疫性疾病中的作用。

Role of the CXCR6/CXCL16 axis in autoimmune diseases.

机构信息

Senior Department of Cardiology, The Sixth Medical Center, Chinese PLA General Hospital, Beijing, China.

Department of Nephrology, First Medical Center of Chinese PLA General Hospital, Beijing, China; State Key Laboratory of Kidney Diseases, Chinese PLA General Hospital, Beijing, China.

出版信息

Int Immunopharmacol. 2023 Aug;121:110530. doi: 10.1016/j.intimp.2023.110530. Epub 2023 Jun 20.

Abstract

The C-X-C motif ligand 16, or CXCL16, is a chemokine that belongs to the ELR - CXC subfamily. Its function is to bind to the chemokine receptor CXCR6, which is a G protein-coupled receptor with 7 transmembrane domains. The CXCR6/CXCL16 axis has been linked to the development of numerous autoimmune diseases and is connected to clinical parameters that reflect disease severity, activity, and prognosis in conditions such as multiple sclerosis, autoimmune hepatitis, rheumatoid arthritis, Crohn's disease, and psoriasis. CXCL16 is expressed in various immune cells, such as dendritic cells, monocytes, macrophages, and B cells. During autoimmune diseases, CXCL16 can facilitate the adhesion of immune cells like monocytes, T cells, NKT cells, and others to endothelial cells and dendritic cells. Additionally, sCXCL16 can regulate the migration of CXCR6-expressing leukocytes, which includes CD8 T cells, CD4 T cells, NK cells, constant natural killer T cells, plasma cells, and monocytes. Further investigation is required to comprehend the intricate interactions between chemokines and the pathogenesis of autoimmune diseases. It remains to be seen whether the CXCR6/CXCL16 axis represents a new target for the treatment of these conditions.

摘要

C-X-C 基序配体 16(C-X-C motif ligand 16,CXCL16)是一种趋化因子,属于 ELR-CXC 亚家族。其功能是与趋化因子受体 CXCR6 结合,后者是一种具有 7 个跨膜结构域的 G 蛋白偶联受体。CXCR6/CXCL16 轴与许多自身免疫性疾病的发展有关,并与多发性硬化症、自身免疫性肝炎、类风湿关节炎、克罗恩病和银屑病等疾病的反映疾病严重程度、活动和预后的临床参数相关。CXCL16 在各种免疫细胞中表达,如树突状细胞、单核细胞、巨噬细胞和 B 细胞。在自身免疫性疾病中,CXCL16 可以促进单核细胞、T 细胞、NKT 细胞等免疫细胞与内皮细胞和树突状细胞的黏附。此外,sCXCL16 可以调节 CXCR6 表达的白细胞的迁移,包括 CD8 T 细胞、CD4 T 细胞、NK 细胞、恒定自然杀伤 T 细胞、浆细胞和单核细胞。需要进一步研究以了解趋化因子与自身免疫性疾病发病机制之间的复杂相互作用。CXCR6/CXCL16 轴是否代表这些疾病治疗的新靶点仍有待观察。

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