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miRNAs 在巨噬细胞介导的肾损伤中的作用。

Role of miRNAs in macrophage-mediated kidney injury.

机构信息

Department of Pharmacy, Affiliated Hospital, Southwest Medical University, Luzhou, 646000, China.

Laboratory of Molecular Pharmacology, Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, 646000, China.

出版信息

Pediatr Nephrol. 2024 Dec;39(12):3397-3410. doi: 10.1007/s00467-024-06414-5. Epub 2024 May 27.

DOI:10.1007/s00467-024-06414-5
PMID:38801452
Abstract

Macrophages, crucial components of the human immune system, can be polarized into M1/M2 phenotypes, each with distinct functions and roles. Macrophage polarization has been reported to be significantly involved in the inflammation and fibrosis observed in kidney injury. MicroRNA (miRNA), a type of short RNA lacking protein-coding function, can inhibit specific mRNA by partially binding to its target mRNA. The intricate association between miRNAs and macrophages has been attracting increasing interest in recent years. This review discusses the role of miRNAs in regulating macrophage-mediated kidney injury. It shows how miRNAs can influence macrophage polarization, thereby altering the biological function of macrophages in the kidney. Furthermore, this review highlights the significance of miRNAs derived from exosomes and extracellular vesicles as a crucial mediator in the crosstalk between macrophages and kidney cells. The potential of miRNAs as treatment applications and biomarkers for macrophage-mediated kidney injury is also discussed.

摘要

巨噬细胞是人体免疫系统的重要组成部分,可极化为 M1/M2 表型,每种表型具有不同的功能和作用。巨噬细胞极化被报道与肾脏损伤中观察到的炎症和纤维化有显著关系。微小 RNA(miRNA)是一种缺乏蛋白编码功能的短 RNA,可通过部分结合其靶 mRNA 来抑制特定的 mRNA。miRNA 与巨噬细胞之间的复杂关系近年来引起了越来越多的关注。本文讨论了 miRNA 在调节巨噬细胞介导的肾脏损伤中的作用。它表明 miRNA 如何影响巨噬细胞极化,从而改变巨噬细胞在肾脏中的生物学功能。此外,本文还强调了外泌体和细胞外囊泡衍生的 miRNA 作为巨噬细胞和肾脏细胞之间串扰的关键介质的重要性。还讨论了 miRNA 作为治疗应用和巨噬细胞介导的肾脏损伤生物标志物的潜力。

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Farnesoid X Receptor Alleviates Cisplatin-Induced Kidney Inflammatory Injury by Inhibiting Tlr4/NF-κB Pathway.法尼酯X受体通过抑制Tlr4/NF-κB通路减轻顺铂诱导的肾脏炎性损伤。
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本文引用的文献

1
Transcription Factor Sox9 Exacerbates Kidney Injury through Inhibition of MicroRNA-96-5p and Activation of the Trib3/IL-6 Axis.转录因子 Sox9 通过抑制 microRNA-96-5p 并激活 Trib3/IL-6 轴加剧肾损伤。
Kidney Blood Press Res. 2023;48(1):611-627. doi: 10.1159/000533544. Epub 2023 Sep 16.
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Macrophage-derived exosomal miR-195a-5p impairs tubular epithelial cells mitochondria in acute kidney injury mice.巨噬细胞衍生的外泌体 miR-195a-5p 损害急性肾损伤小鼠肾小管上皮细胞的线粒体。
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Yi-Shen-Hua-Shi granules inhibit diabetic nephropathy by ameliorating podocyte injury induced by macrophage-derived exosomes.
急性和慢性肾病中的固有免疫细胞。
Nat Rev Nephrol. 2025 Apr 22. doi: 10.1038/s41581-025-00958-x.
益肾化湿颗粒通过改善巨噬细胞来源外泌体诱导的足细胞损伤来抑制糖尿病肾病。
Front Pharmacol. 2022 Nov 25;13:962606. doi: 10.3389/fphar.2022.962606. eCollection 2022.
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Role of miR-379 in high-fat diet-induced kidney injury and dysfunction.miR-379 在高脂饮食诱导的肾损伤和功能障碍中的作用。
Am J Physiol Renal Physiol. 2022 Dec 1;323(6):F686-F699. doi: 10.1152/ajprenal.00213.2022. Epub 2022 Oct 13.
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Mesenchymal stem cell-derived exosome-educated macrophages alleviate systemic lupus erythematosus by promoting efferocytosis and recruitment of IL-17 regulatory T cell.间充质干细胞衍生的外泌体诱导的巨噬细胞通过促进吞噬作用和募集 IL-17 调节性 T 细胞缓解系统性红斑狼疮。
Stem Cell Res Ther. 2022 Sep 24;13(1):484. doi: 10.1186/s13287-022-03174-7.
6
Circular RNA ACTR2 activates M2 polarization of macrophages through activating Yes-associated protein signalling and contributes to renal fibrosis.环状 RNA ACTR2 通过激活 Yes 相关蛋白信号通路激活巨噬细胞 M2 极化,并促进肾脏纤维化。
Immunology. 2022 Dec;167(4):606-621. doi: 10.1111/imm.13558. Epub 2022 Sep 7.
7
LNA-anti-miR-150 alleviates renal interstitial fibrosis by reducing pro-inflammatory M1/M2 macrophage polarization.LNA-anti-miR-150 通过减少促炎 M1/M2 巨噬细胞极化来减轻肾间质纤维化。
Front Immunol. 2022 Aug 5;13:913007. doi: 10.3389/fimmu.2022.913007. eCollection 2022.
8
WDR74 facilitates TGF-β/Smad pathway activation to promote M2 macrophage polarization and diabetic foot ulcer wound healing in mice.WDR74 促进 TGF-β/Smad 通路激活,促进 M2 巨噬细胞极化和糖尿病足溃疡愈合。
Cell Biol Toxicol. 2023 Aug;39(4):1577-1591. doi: 10.1007/s10565-022-09748-8. Epub 2022 Aug 19.
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Exosomal miR-7002-5p derived from highglucose-induced macrophages suppresses autophagy in tubular epithelial cells by targeting Atg9b.高糖诱导的巨噬细胞来源的外泌体 miR-7002-5p 通过靶向 Atg9b 抑制肾小管上皮细胞自噬。
FASEB J. 2022 Sep;36(9):e22501. doi: 10.1096/fj.202200550RR.
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P2Y12 inhibitor clopidogrel inhibits renal fibrosis by blocking macrophage-to-myofibroblast transition.P2Y12 抑制剂氯吡格雷通过阻断巨噬细胞向肌成纤维细胞转化来抑制肾纤维化。
Mol Ther. 2022 Sep 7;30(9):3017-3033. doi: 10.1016/j.ymthe.2022.06.019. Epub 2022 Jul 5.