Yu Siming, Han Zehui, Li Chunsheng, Lu Xinxin, Li Yue, Yuan Xingxing, Guo Dandan
Department of Nephrology II, First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin 150036, China.
First Clinical Medical College, Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Mediators Inflamm. 2025 May 2;2025:8140479. doi: 10.1155/mi/8140479. eCollection 2025.
Diabetic nephropathy (DN) is a leading cause of chronic kidney disease and end-stage renal failure worldwide. Podocytes, essential components of the glomerular filtration barrier (GFB), are profoundly affected in the diabetic milieu, resulting in structural and functional alterations. Concurrently, macrophages, pivotal innate immune cells, infiltrate the diabetic kidney and exhibit diverse activation states influenced by the local environment, playing a crucial role in kidney physiology and pathology. This review synthesizes current insights into how the dynamic cross talk between these two cell types contributes to the progression of DN, exploring the molecular and cellular mechanisms underlying this interaction, with a particular focus on how macrophages influence podocyte survival through various forms of cell death, including apoptosis, pyroptosis, and autophagy. The review also discusses the potential of targeting macrophages to develop more effective treatments for DN.
糖尿病肾病(DN)是全球慢性肾脏病和终末期肾衰竭的主要原因。足细胞是肾小球滤过屏障(GFB)的重要组成部分,在糖尿病环境中受到严重影响,导致结构和功能改变。同时,巨噬细胞作为关键的固有免疫细胞,浸润糖尿病肾脏并呈现受局部环境影响的多种激活状态,在肾脏生理和病理过程中发挥关键作用。本综述综合了目前对于这两种细胞类型之间的动态相互作用如何促进DN进展的见解,探讨了这种相互作用的分子和细胞机制,特别关注巨噬细胞如何通过包括凋亡、焦亡和自噬在内的各种细胞死亡形式影响足细胞存活。该综述还讨论了以巨噬细胞为靶点开发更有效DN治疗方法的潜力。