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聚焦巨噬细胞:糖尿病肾病的关键驱动因素与治疗机遇

Macrophages in Focus: Key Drivers and Therapeutic Opportunities in Diabetic Kidney Disease.

作者信息

Zhao Hui, Guo Jia

机构信息

Department of Nephrology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, China.

Key Laboratory of Precision Diagnosis and Treatment for Chronic Kidney Disease in Henan Province, Zhengzhou, Henan, 450052, China.

出版信息

Int J Biol Sci. 2025 Jul 11;21(10):4647-4662. doi: 10.7150/ijbs.112737. eCollection 2025.

DOI:10.7150/ijbs.112737
PMID:40765824
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12320494/
Abstract

Diabetic kidney disease (DKD), a common microvascular complication of diabetes, has emerged as the leading cause of end-stage renal disease (ESRD), with its prevalence increasing annually, thereby constituting a global epidemiological crisis. Despite this, the search for effective therapeutic strategies remains challenging, underscoring the urgent need for innovative treatments. In recent years, numerous studies have highlighted the role of inflammation in DKD progression, with fibrosis serving as a critical mechanism driving DKD towards ESRD. Intervening in these core processes may reveal new avenues for the etiology and management of DKD. Macrophages, immune cells derived from monocytes, possess phagocytic and digestive functions and play integral roles in tissue and organ development, homeostasis, as well as tissue repair and regeneration. Emerging research suggests that macrophages are crucial in DKD progression and renal injury, thus attracting significant academic attention. This review highlights the role and mechanisms of macrophages in the inflammatory and fibrotic processes in DKD. It also explores current therapeutic approaches targeting macrophages. In light of recent research, we propose that macrophages-focused interventions present a promising therapeutic avenue for DKD.

摘要

糖尿病肾病(DKD)是糖尿病常见的微血管并发症,已成为终末期肾病(ESRD)的主要原因,其患病率逐年上升,从而构成了一场全球流行病学危机。尽管如此,寻找有效的治疗策略仍然具有挑战性,这凸显了对创新治疗方法的迫切需求。近年来,大量研究强调了炎症在DKD进展中的作用,纤维化是推动DKD发展为ESRD的关键机制。干预这些核心过程可能会为DKD的病因学和管理揭示新的途径。巨噬细胞是源自单核细胞的免疫细胞,具有吞噬和消化功能,在组织和器官发育、内环境稳态以及组织修复和再生中发挥着不可或缺的作用。新出现的研究表明,巨噬细胞在DKD进展和肾损伤中至关重要,因此引起了学术界的广泛关注。本综述重点介绍了巨噬细胞在DKD炎症和纤维化过程中的作用及机制。还探讨了目前针对巨噬细胞的治疗方法。鉴于最近的研究,我们认为以巨噬细胞为重点的干预措施为DKD提供了一条有前景的治疗途径。

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本文引用的文献

1
Single-nucleus RNA sequencing reveals ARHGAP28 expression of podocytes as a biomarker in human diabetic nephropathy.单核RNA测序揭示足细胞中ARHGAP28的表达作为人类糖尿病肾病的生物标志物。
Open Med (Wars). 2025 Apr 2;20(1):20251146. doi: 10.1515/med-2025-1146. eCollection 2025.
2
A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages.过氧化物酶 2 通过激活经典激活型巨噬细胞在糖尿病肾病进展中的新作用。
Sci Rep. 2024 Nov 16;14(1):28258. doi: 10.1038/s41598-024-79678-4.
3
[Potential pathways for traditional Chinese medicine intervention in diabetic kidney disease: macrophage polarization].
[中药干预糖尿病肾病的潜在途径:巨噬细胞极化]
Zhongguo Zhong Yao Za Zhi. 2024 Aug;49(15):4044-4053. doi: 10.19540/j.cnki.cjcmm.20240412.708.
4
Tonabersat suppresses priming/activation of the NOD-like receptor protein-3 (NLRP3) inflammasome and decreases renal tubular epithelial-to-macrophage crosstalk in a model of diabetic kidney disease.托纳布沙抑制 NOD 样受体蛋白-3(NLRP3)炎症小体的引发/激活,并减少糖尿病肾病模型中肾小管上皮细胞向巨噬细胞的细胞间通讯。
Cell Commun Signal. 2024 Jul 5;22(1):351. doi: 10.1186/s12964-024-01728-1.
5
Single-cell RNA transcriptomic reveal the mechanism of MSC derived small extracellular vesicles against DKD fibrosis.单细胞 RNA 转录组揭示 MSC 来源的小细胞外囊泡对抗 DKD 纤维化的机制。
J Nanobiotechnology. 2024 Jun 18;22(1):339. doi: 10.1186/s12951-024-02613-2.
6
Targeting Macrophages: Therapeutic Approaches in Diabetic Kidney Disease.靶向巨噬细胞:糖尿病肾病的治疗方法
Int J Mol Sci. 2024 Apr 15;25(8):4350. doi: 10.3390/ijms25084350.
7
25-Hydroxycholesterol regulates lysosome AMP kinase activation and metabolic reprogramming to educate immunosuppressive macrophages.25-羟胆固醇调节溶酶体 AMP 激酶激活和代谢重编程以诱导免疫抑制性巨噬细胞。
Immunity. 2024 May 14;57(5):1087-1104.e7. doi: 10.1016/j.immuni.2024.03.021. Epub 2024 Apr 18.
8
A novel role for the ROS-ATM-Chk2 axis mediated metabolic and cell cycle reprogramming in the M1 macrophage polarization.ROS-ATM-Chk2 轴在 M1 巨噬细胞极化中代谢和细胞周期重编程的新作用。
Redox Biol. 2024 Apr;70:103059. doi: 10.1016/j.redox.2024.103059. Epub 2024 Feb 1.
9
Myricetin induces M2 macrophage polarization to alleviate renal tubulointerstitial fibrosis in diabetic nephropathy PI3K/Akt pathway.杨梅素通过PI3K/Akt信号通路诱导M2巨噬细胞极化以减轻糖尿病肾病中的肾小管间质纤维化。
World J Diabetes. 2024 Jan 15;15(1):105-125. doi: 10.4239/wjd.v15.i1.105.
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Renal macrophages monitor and remove particles from urine to prevent tubule obstruction.肾脏巨噬细胞监测并清除尿液中的颗粒,以防止肾小管阻塞。
Immunity. 2024 Jan 9;57(1):106-123.e7. doi: 10.1016/j.immuni.2023.12.003. Epub 2023 Dec 29.