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调节性固有淋巴细胞抑制固有免疫,减少肾缺血/再灌注损伤。

Regulatory innate lymphoid cells suppress innate immunity and reduce renal ischemia/reperfusion injury.

机构信息

Centre for Transplant and Renal Research, Westmead Institute for Medical Research, The University of Sydney, Sydney, New South Wales, Australia; Laboratory of Immunology and Targeted Therapy, School of Laboratory Medicine, Xinxiang Medical University, Henan, China.

Centre for Transplant and Renal Research, Westmead Institute for Medical Research, The University of Sydney, Sydney, New South Wales, Australia; Department of Nephrology, The Second Hospital of Anhui Medical University, Anhui, China.

出版信息

Kidney Int. 2020 Jan;97(1):130-142. doi: 10.1016/j.kint.2019.07.019. Epub 2019 Aug 23.

Abstract

Innate lymphoid cells are a recently recognized group of immune cells with critical roles in tissue homeostasis and inflammation. Regulatory innate lymphoid cells are a newly identified subset of innate lymphoid cells, which play a suppressive role in the innate immune response, favoring the resolution of intestinal inflammation. However, the expression and role of regulatory innate lymphoid cells in kidney has not been reported. Here, we show that regulatory innate lymphoid cells are present in both human and mouse kidney, express similar surface markers and form a similar proportion of total kidney innate lymphoid cells. Regulatory innate lymphoid cells from kidney were expanded in vitro with a combination of IL-2, IL-7 and transforming growth factor-β. These cells exhibited immunosuppressive effects on innate immune cells via secretion of IL-10 and transforming growth factor-β. Moreover, treatment with IL-2/IL-2 antibody complexes (IL-2C) promoted expansion of regulatory innate lymphoid cells in vivo, and prevent renal ischemia/reperfusion injury in Rag-/- mice that lack adaptive immune cells including Tregs. Depletion of regulatory innate lymphoid cells with anti-CD25 antibody abolished the beneficial effects of IL-2C in the Rag-/- mice. Adoptive transfer of ex vivo expanded regulatory innate lymphoid cells improved renal function and attenuated histologic damage when given before or after induction of ischemia/reperfusion injury in association with reduction of neutrophil infiltration and induction of reparative M2 macrophages in kidney. Thus, our study shows that regulatory innate lymphoid cells suppress innate renal inflammation and ischemia/reperfusion injury.

摘要

固有淋巴细胞是一类新近被发现的免疫细胞,在组织稳态和炎症反应中具有关键作用。调节性固有淋巴细胞是固有淋巴细胞的一个新亚群,在固有免疫反应中发挥抑制作用,有利于肠道炎症的消退。然而,调节性固有淋巴细胞在肾脏中的表达和作用尚未见报道。在这里,我们发现在人和鼠的肾脏中均存在调节性固有淋巴细胞,其表达相似的表面标志物,并且构成肾脏固有淋巴细胞的比例相似。通过联合使用 IL-2、IL-7 和转化生长因子-β,可在体外扩增肾脏来源的调节性固有淋巴细胞。这些细胞通过分泌 IL-10 和转化生长因子-β对固有免疫细胞发挥免疫抑制作用。此外,用 IL-2/IL-2 抗体复合物(IL-2C)处理可促进 Rag-/- 小鼠(缺乏包括 Treg 在内的适应性免疫细胞)体内调节性固有淋巴细胞的扩增,并预防肾缺血/再灌注损伤。用抗 CD25 抗体耗竭调节性固有淋巴细胞可消除 IL-2C 在 Rag-/- 小鼠中的有益作用。在诱导缺血/再灌注损伤之前或之后给予体外扩增的调节性固有淋巴细胞的过继转移可改善肾功能并减轻组织学损伤,同时减少中性粒细胞浸润和诱导肾脏中修复性 M2 巨噬细胞。因此,我们的研究表明,调节性固有淋巴细胞可抑制固有肾脏炎症和缺血/再灌注损伤。

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