Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN (Y.J., L.M.G., L.O.L.).
Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN (A.L.).
Hypertension. 2023 Jan;80(1):35-42. doi: 10.1161/HYPERTENSIONAHA.122.19431. Epub 2022 Nov 11.
The inflammatory response is a major pathological feature in most kidney diseases and often evokes compensatory mechanisms. Recent evidence suggests that TSG-6 (tumor necrosis factor-α-stimulated gene/protein-6) plays a pivotal role in anti-inflammation in various renal diseases, including immune-mediated and nonimmune-mediated renal diseases. TSG-6 has a diverse repertoire of anti-inflammatory functions: it potentiates antiplasmin activity of IαI (inter-α-inhibitor) by binding to its light chain, crosslinks hyaluronan to promote its binding to cell surface receptor CD44, and thereby regulate the migration and adhesion of lymphocytes, inhibits chemokine-stimulated transendothelial migration of neutrophils by directly interacting with the glycosaminoglycan binding site of CXCL8 (CXC motif chemokine ligand-8), and upregulates COX-2 (cyclooxygenase-2) to produce anti-inflammatory metabolites. Hopefully, further developments can target this anti-inflammatory molecule to the kidney and harness its remedial properties. This review provides an overview of the emerging role of TSG-6 in blunting renal inflammation.
炎症反应是大多数肾脏疾病的主要病理特征,常引发代偿机制。最近的证据表明,TSG-6(肿瘤坏死因子-α刺激基因/蛋白-6)在各种肾脏疾病(包括免疫介导和非免疫介导的肾脏疾病)的抗炎中发挥关键作用。TSG-6 具有多种抗炎功能:它通过与轻链结合增强 IαI(α-抑制因子)的抗纤溶酶活性,交联透明质酸以促进其与细胞表面受体 CD44 的结合,从而调节淋巴细胞的迁移和黏附,通过直接与 CXCL8(CXC 基序趋化因子配体-8)的糖胺聚糖结合位点相互作用抑制趋化因子刺激的中性粒细胞跨内皮迁移,并上调 COX-2(环氧化酶-2)产生抗炎代谢物。希望进一步的研究能将这种抗炎分子靶向肾脏,并利用其治疗特性。本文综述了 TSG-6 在肾脏炎症中的作用。