Lin Da-Wei, Yang Tsung-Ming, Ho Cheng, Shih Ya-Hsueh, Lin Chun-Liang, Hsu Yung-Chien
Department of Internal Medicine, St. Martin De Porres Hospital, Chiayi City 60069, Taiwan.
Division of Pulmonary and Critical Care Medicine, Chang Gung Memorial Hospital, Chiayi County 61363, Taiwan.
Int J Mol Sci. 2024 Apr 15;25(8):4350. doi: 10.3390/ijms25084350.
Diabetes is not solely a metabolic disorder but also involves inflammatory processes. The immune response it incites is a primary contributor to damage in target organs. Research indicates that during the initial phases of diabetic nephropathy, macrophages infiltrate the kidneys alongside lymphocytes, initiating a cascade of inflammatory reactions. The interplay between macrophages and other renal cells is pivotal in the advancement of kidney disease within a hyperglycemic milieu. While M1 macrophages react to the inflammatory stimuli induced by elevated glucose levels early in the disease progression, their subsequent transition to M2 macrophages, which possess anti-inflammatory and tissue repair properties, also contributes to fibrosis in the later stages of nephropathy by transforming into myofibroblasts. Comprehending the diverse functions of macrophages in diabetic kidney disease and regulating their activity could offer therapeutic benefits for managing this condition.
糖尿病不仅是一种代谢紊乱疾病,还涉及炎症过程。它引发的免疫反应是导致靶器官损伤的主要因素。研究表明,在糖尿病肾病的初始阶段,巨噬细胞与淋巴细胞一起浸润肾脏,引发一系列炎症反应。在高血糖环境中,巨噬细胞与其他肾细胞之间的相互作用对肾脏疾病的进展至关重要。在疾病进展早期,M1巨噬细胞对葡萄糖水平升高诱导的炎症刺激作出反应,随后它们转变为具有抗炎和组织修复特性的M2巨噬细胞,而M2巨噬细胞通过转化为肌成纤维细胞,在肾病后期也会导致纤维化。了解巨噬细胞在糖尿病肾病中的多种功能并调节其活性,可能为治疗这种疾病带来益处。