Department of Nephrology, Qidong People's Hospital, Nantong, Jiangsu Province, China.
Department of Pain, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, China.
Rev Physiol Biochem Pharmacol. 2020;177:1-24. doi: 10.1007/112_2020_21.
Renal fibrosis is the final pathological process common to any ongoing, chronic kidney injury or maladaptive repair. Renal fibrosis is considered to be closely related to various cell types, such as fibroblasts, myofibroblasts, T cells, and other inflammatory cells. Multiple types of cells regulate renal fibrosis through the recruitment, proliferation, and activation of fibroblasts, and the production of the extracellular matrix. Cell trafficking is orchestrated by a family of small proteins called chemokines. Chemokines are cytokines with chemotactic properties, which are classified into 4 groups: CXCL, CCL, CX3CL, and XCL. Similarly, chemokine receptors are G protein-coupled seven-transmembrane receptors classified into 4 groups: XCR, CCR, CXCR, and CX3CR. Chemokine receptors are also implicated in the infiltration, differentiation, and survival of functional cells, triggering inflammation that leads to fibrosis development. In this review, we summarize the different chemokine receptors involved in the processes of fibrosis in different cell types. Further studies are required to identify the molecular mechanisms of chemokine signaling that contribute to renal fibrosis.
肾纤维化是任何持续的、慢性的肾损伤或适应性修复所共有的终末病理过程。肾纤维化被认为与多种细胞类型密切相关,如成纤维细胞、肌成纤维细胞、T 细胞和其他炎症细胞。多种类型的细胞通过招募、增殖和激活成纤维细胞以及产生细胞外基质来调节肾纤维化。细胞迁移是由一组称为趋化因子的小蛋白家族协调的。趋化因子是具有趋化性的细胞因子,分为 4 组:CXCL、CCL、CX3CL 和 XCL。同样,趋化因子受体是 G 蛋白偶联的七跨膜受体,分为 4 组:XCR、CCR、CXCR 和 CX3CR。趋化因子受体也参与功能性细胞的浸润、分化和存活,引发炎症,导致纤维化的发展。在这篇综述中,我们总结了不同细胞类型中参与纤维化过程的不同趋化因子受体。需要进一步研究以确定趋化因子信号转导的分子机制,这些机制有助于肾纤维化的发生。