Department of Medicine and Therapeutics, and Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, China.
J Am Soc Nephrol. 2011 May;22(5):802-9. doi: 10.1681/ASN.2010050510. Epub 2011 Apr 7.
The main function of chemokines is to guide inflammatory cells in their migration to sites of inflammation. During the last 2 decades, an expanding number of chemokines and their receptors have driven broad inquiry into how inflammatory cells are recruited in a variety of diseases. Although this review focuses on chemokines and their receptors in renal injury, proinflammatory IL-17, TGFβ, and TWEAK signaling pathways also play a critical role in their expression. Recent studies in transgenic mice as well as blockade of chemokine signaling by neutralizing ligands or receptor antagonists now allow direct interrogation of chemokine action. The emerging role of regulatory T cells and Th17 cells during renal injury also forges tight relationships between chemokines and T cell infiltration in the development of kidney disease. As chemokine receptor blockade inches toward clinical use, the field remains an attractive area with potential for unexpected opportunity in the future.
趋化因子的主要功能是指导炎症细胞向炎症部位迁移。在过去的 20 年中,越来越多的趋化因子及其受体的研究推动了人们对各种疾病中炎症细胞募集的广泛探究。尽管本综述重点关注了趋化因子及其在肾脏损伤中的受体,但促炎细胞因子 IL-17、TGFβ 和 TWEAK 信号通路也在它们的表达中发挥着关键作用。最近在转基因小鼠中的研究以及通过中和配体或受体拮抗剂阻断趋化因子信号,现在可以直接研究趋化因子的作用。在肾脏损伤过程中调节性 T 细胞和 Th17 细胞的新兴作用也在趋化因子与 T 细胞浸润在肾脏疾病发展之间建立了紧密的关系。随着趋化因子受体阻断向临床应用的推进,该领域仍然具有吸引力,未来可能会有意外的机会。