Dousdampanis Periklis, Aggeletopoulou Ioanna, Mouzaki Athanasia
Department of Nephrology, Saint Andrews General Hospital of Patras, Patras, Greece.
Laboratory of Immunohematology, Department of Internal Medicine, Medical School, University of Patras, Patras, Greece.
Front Immunol. 2025 Jan 10;15:1534823. doi: 10.3389/fimmu.2024.1534823. eCollection 2024.
Obesity is a rapidly growing health problem worldwide, affecting both adults and children and increasing the risk of chronic diseases such as type 2 diabetes, hypertension and cardiovascular disease (CVD). In addition, obesity is closely linked to chronic kidney disease (CKD) by either exacerbating diabetic complications or directly causing kidney damage. Obesity-related CKD is characterized by proteinuria, lipid accumulation, fibrosis and glomerulosclerosis, which can gradually impair kidney function. Among the immune cells of the innate and adaptive immune response involved in the pathogenesis of obesity-related diseases, macrophages play a crucial role in the inflammation associated with CKD. In obese individuals, macrophages enter a pro-inflammatory state known as M1 polarization, which contributes to chronic inflammation. This polarization promotes tissue damage, inflammation and fibrosis, leading to progressive loss of kidney function. In addition, macrophage-induced oxidative stress is a key feature of CKD as it also promotes cell damage and inflammation. Macrophages also contribute to insulin resistance in type 2 diabetes by releasing inflammatory molecules that impair glucose metabolism, complicating the management of diabetes in obese patients. Hypertension and atherosclerosis, which are often associated with obesity, also contribute to the progression of CKD via immune and inflammatory pathways. Macrophages influence blood pressure regulation and contribute to vascular inflammation, particularly via the renin-angiotensin system. In atherosclerosis, macrophages accumulate in arterial plaques, leading to chronic inflammation and plaque instability, which may increase the risk of CVD in CKD patients. This review focuses on the involvement of macrophages in CKD and highlights their role as a critical link between CKD and other pathologies. Targeting macrophage polarization and the ensuing macrophage-induced inflammation could be an effective therapeutic strategy for CKD and related diseases and improve outcomes for patients with obesity-related kidney disease.
肥胖是全球范围内迅速增长的健康问题,影响着成人和儿童,并增加了2型糖尿病、高血压和心血管疾病(CVD)等慢性病的风险。此外,肥胖通过加剧糖尿病并发症或直接导致肾脏损伤,与慢性肾脏病(CKD)密切相关。肥胖相关的CKD的特征是蛋白尿、脂质蓄积、纤维化和肾小球硬化,这些可逐渐损害肾功能。在参与肥胖相关疾病发病机制的先天性和适应性免疫反应的免疫细胞中,巨噬细胞在与CKD相关的炎症中起关键作用。在肥胖个体中,巨噬细胞进入一种称为M1极化的促炎状态,这会导致慢性炎症。这种极化促进组织损伤、炎症和纤维化,导致肾功能逐渐丧失。此外,巨噬细胞诱导的氧化应激是CKD的一个关键特征,因为它也促进细胞损伤和炎症。巨噬细胞还通过释放损害葡萄糖代谢的炎症分子,导致2型糖尿病患者的胰岛素抵抗,使肥胖患者的糖尿病管理复杂化。通常与肥胖相关的高血压和动脉粥样硬化,也通过免疫和炎症途径促进CKD的进展。巨噬细胞影响血压调节,并导致血管炎症,特别是通过肾素-血管紧张素系统。在动脉粥样硬化中,巨噬细胞积聚在动脉斑块中,导致慢性炎症和斑块不稳定,这可能增加CKD患者发生CVD的风险。本综述重点关注巨噬细胞在CKD中的作用,并强调它们作为CKD与其他病理之间关键联系的作用。针对巨噬细胞极化及随之而来的巨噬细胞诱导的炎症,可能是治疗CKD及相关疾病的有效策略,并改善肥胖相关肾病患者的预后。