The role of extracellular vesicles in kidney disease progression.

IF 2.9 3区 医学 Q1 UROLOGY & NEPHROLOGY
Ran Kim, Tae Min Kim
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引用次数: 0

Abstract

Extracellular vesicles (EVs) are nanosized membranous particles released by nearly all cell types, playing a crucial role in mediating cell-to-cell communication. The molecular profile of EVs often reflects that of their originating cells, rendering them valuable for therapeutic and diagnostic purposes. The kidney comprises various cell types, and urinary EVs are predominantly produced from tubular, glomerular, and urinary bladder cells. Within the nephron, EVs produced from the upper segments, such as glomerular tufts and proximal tubules, can be taken up by their downstream counterparts, thereby altering the physiology of recipient cells. Recent studies have demonstrated that this proximal-distal intra-nephron crosstalk via EVs is crucial for normal kidney physiology. Additionally, EVs from interstitial cells (e.g., fibroblasts and macrophages) have been demonstrated to mediate the exacerbation of kidney damage. This review provides up-to-date findings on the function of renal EVs during the progression of renal diseases. Furthermore, we discussed future directions to use the clinical potential of renal EVs as an early biomarker for renal disorders.

细胞外囊泡在肾脏疾病进展中的作用。
细胞外囊泡(EVs)是由几乎所有细胞类型释放的纳米级膜状颗粒,在介导细胞间通讯中起着至关重要的作用。电动汽车的分子特征通常反映其起源细胞的分子特征,使其具有治疗和诊断目的的价值。肾脏由多种细胞类型组成,尿内ev主要由肾小管细胞、肾小球细胞和膀胱细胞产生。在肾元内,由肾小球丛和近端小管等上节段产生的EVs可被下游对应的EVs吸收,从而改变受体细胞的生理机能。最近的研究表明,这种通过ev的近端-远端肾元内串扰对正常肾脏生理至关重要。此外,来自间质细胞(如成纤维细胞和巨噬细胞)的ev已被证明可以介导肾损伤的加剧。本文综述了肾脏疾病进展过程中肾脏ev功能的最新研究结果。此外,我们还讨论了利用肾脏ev作为肾脏疾病早期生物标志物的临床潜力的未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.60
自引率
10.00%
发文量
77
审稿时长
10 weeks
期刊介绍: Kidney Research and Clinical Practice (formerly The Korean Journal of Nephrology; ISSN 1975-9460, launched in 1982), the official journal of the Korean Society of Nephrology, is an international, peer-reviewed journal published in English. Its ISO abbreviation is Kidney Res Clin Pract. To provide an efficient venue for dissemination of knowledge and discussion of topics related to basic renal science and clinical practice, the journal offers open access (free submission and free access) and considers articles on all aspects of clinical nephrology and hypertension as well as related molecular genetics, anatomy, pathology, physiology, pharmacology, and immunology. In particular, the journal focuses on translational renal research that helps bridging laboratory discovery with the diagnosis and treatment of human kidney disease. Topics covered include basic science with possible clinical applicability and papers on the pathophysiological basis of disease processes of the kidney. Original researches from areas of intervention nephrology or dialysis access are also welcomed. Major article types considered for publication include original research and reviews on current topics of interest. Accepted manuscripts are granted free online open-access immediately after publication, which permits its users to read, download, copy, distribute, print, search, or link to the full texts of its articles to facilitate access to a broad readership. Circulation number of print copies is 1,600.
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