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糖尿病肾病肾小管损伤中外泌体的研究进展。

Research progress on extracellular vesicles in the renal tubular injury of diabetic kidney disease.

机构信息

Department of Nephrology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, China.

Department of Nephrology, Binzhou People's Hospital Affiliated to Shandong First Medical University, Binzhou, China.

出版信息

Front Endocrinol (Lausanne). 2023 Sep 4;14:1257430. doi: 10.3389/fendo.2023.1257430. eCollection 2023.

DOI:10.3389/fendo.2023.1257430
PMID:37732129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10507342/
Abstract

Diabetic kidney disease (DKD) is a severe microvascular complication of diabetes and is a chronic progressive condition. It is also a common cause of end-stage renal disease (ESRD), which is characterized by proteinuria or a progressive decline in the glomerular filtration rate. Due to their dependence on high-energy and aerobic metabolism, renal tubules are more susceptible to the metabolic disturbances associated with DKD, leading to inflammation and fibrosis. Consequently, tubular injury has become a recent research focus, and significant advancements have been made in studying the role of extracellular vesicles in DKD-associated tubular injury. This review aimed to elucidate the mechanisms and potential applications of different types of extracellular vesicles in tubular injury in DKD to provide new insights for the prevention and treatment of DKD.

摘要

糖尿病肾病(DKD)是糖尿病严重的微血管并发症,是一种慢性进行性疾病。它也是终末期肾病(ESRD)的常见原因,其特征是蛋白尿或肾小球滤过率逐渐下降。由于肾小管依赖于高能和需氧代谢,因此更容易受到与 DKD 相关的代谢紊乱的影响,导致炎症和纤维化。因此,管状损伤已成为近期研究的重点,并且在研究细胞外囊泡在 DKD 相关管状损伤中的作用方面取得了重大进展。本综述旨在阐明不同类型的细胞外囊泡在 DKD 管状损伤中的机制和潜在应用,为 DKD 的预防和治疗提供新的思路。

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Research progress on extracellular vesicles in the renal tubular injury of diabetic kidney disease.糖尿病肾病肾小管损伤中外泌体的研究进展。
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本文引用的文献

1
Extracellular vesicles in kidney disease.肾脏疾病中的细胞外囊泡。
Nat Rev Nephrol. 2022 Aug;18(8):499-513. doi: 10.1038/s41581-022-00586-9. Epub 2022 May 31.
2
Stem cell-derived and circulating exosomal microRNAs as new potential tools for diabetic nephropathy management.干细胞衍生和循环的外泌体 microRNAs 作为糖尿病肾病管理的新潜在工具。
Stem Cell Res Ther. 2022 Jan 24;13(1):25. doi: 10.1186/s13287-021-02696-w.
3
Tubular epithelial cell-to-macrophage communication forms a negative feedback loop via extracellular vesicle transfer to promote renal inflammation and apoptosis in diabetic nephropathy.管状上皮细胞与巨噬细胞的通讯通过细胞外囊泡转移形成负反馈回路,从而促进糖尿病肾病中的肾脏炎症和细胞凋亡。
Theranostics. 2022 Jan 1;12(1):324-339. doi: 10.7150/thno.63735. eCollection 2022.
4
Autocrine Exosomal Fibulin-1 as a Target of MiR-1269b Induces Epithelial-Mesenchymal Transition in Proximal Tubule in Diabetic Nephropathy.自分泌外泌体纤连蛋白-1作为miR-1269b的靶点可诱导糖尿病肾病近端小管上皮-间质转化
Front Cell Dev Biol. 2021 Dec 17;9:789716. doi: 10.3389/fcell.2021.789716. eCollection 2021.
5
Diabetic Nephropathy: Challenges in Pathogenesis, Diagnosis, and Treatment.糖尿病肾病:发病机制、诊断和治疗的挑战。
Biomed Res Int. 2021 Jul 8;2021:1497449. doi: 10.1155/2021/1497449. eCollection 2021.
6
Extracellular Vesicles From High Glucose-Treated Podocytes Induce Apoptosis of Proximal Tubular Epithelial Cells.高糖处理的足细胞分泌的细胞外囊泡可诱导近端肾小管上皮细胞凋亡。
Front Physiol. 2020 Nov 2;11:579296. doi: 10.3389/fphys.2020.579296. eCollection 2020.
7
Diabetic Kidney Disease.糖尿病肾病
Prim Care. 2020 Dec;47(4):645-659. doi: 10.1016/j.pop.2020.08.004. Epub 2020 Sep 23.
8
Podocyte-derived extracellular vesicles mediate renal proximal tubule cells dedifferentiation via microRNA-221 in diabetic nephropathy.足细胞来源的细胞外囊泡通过微小 RNA-221 介导糖尿病肾病中肾小管近端细胞去分化。
Mol Cell Endocrinol. 2020 Dec 1;518:111034. doi: 10.1016/j.mce.2020.111034. Epub 2020 Sep 12.
9
Inhibiting Rab27a in renal tubular epithelial cells attenuates the inflammation of diabetic kidney disease through the miR-26a-5p/CHAC1/NF-kB pathway.在肾小管上皮细胞中抑制 Rab27a 通过 miR-26a-5p/CHAC1/NF-κB 通路减轻糖尿病肾病的炎症反应。
Life Sci. 2020 Nov 15;261:118347. doi: 10.1016/j.lfs.2020.118347. Epub 2020 Aug 25.
10
Decreased secretion and profibrotic activity of tubular exosomes in diabetic kidney disease.糖尿病肾病中管状外泌体分泌减少和促纤维化活性增强。
Am J Physiol Renal Physiol. 2020 Oct 1;319(4):F664-F673. doi: 10.1152/ajprenal.00292.2020. Epub 2020 Jul 27.