Future embracing: exosomes driving a revolutionary approach to the diagnosis and treatment of idiopathic membranous nephropathy
Open Access
- 8 August 2024
- journal article
- review article
- Published by Springer Nature in Journal of Nanobiotechnology
- Vol. 22 (1) , 1-32
Abstract
Membranous nephropathy (MN) is a leading cause of nephrotic syndrome in adults and is associated with high rates of end-stage renal disease. Early detection and precise interventions are crucial for improving patient prognosis and quality of life. However, the current diagnosis primarily relies on renal biopsies and traditional biomarkers, which have limitations. Additionally, targeted therapeutic strategies are lacking. Exosomes, small vesicles that facilitate intercellular communication, have emerged as potential noninvasive diagnostic markers due to their stability, diverse cargo, and rapid detectability. They also hold promise as carriers for gene and drug delivery, presenting innovative opportunities in renal disease prognosis and treatment. However, research on exosomes in the context of idiopathic membranous nephropathy (IMN) remains limited, with a focus on exploring urinary exosomes as IMN markers. In this review, we summarize the current status of MN diagnosis and treatment, highlight the fundamental characteristics of exosomes, and discuss recent advancements in their application to IMN diagnosis and therapy. We provide insights into the clinical prospects of exosomes in IMN and acknowledge potential challenges. This article aims to offer forward-looking insights into the future of exosome-mediated IMN diagnosis and treatment, indicating a revolutionary transformation in this field.Keywords
Funding Information
- National Natural Science Foundation of China (No. 2019YFC1709401)
- Tianjin Municipal Health Commission (No. 2021012)
- Postdoctoral Fellowship Program of CPSF (No. GZC20233233)
This publication has 227 references indexed in Scilit:
- Migrasomes and exosomes; different types of messaging vesicles in podocytesCell Biology International, 2021
- M2 macrophage‐derived exosomal miR‐25‐3p improves high glucose‐induced podocytes injury through activation autophagy via inhibiting DUSP1 expressionIUBMB Life, 2020
- Exosomes from human‐bone‐marrow‐derived mesenchymal stem cells protect against renal ischemia/reperfusion injury via transferring miR‐199a‐3pJournal of Cellular Physiology, 2019
- Upregulated microRNAs in membranous glomerulonephropathy are associated with significant downregulation of IL6 and MYC mRNAsJournal of Cellular Physiology, 2018
- Interplay between miRNAs and human diseasesJournal of Cellular Physiology, 2017
- Differential expression of urinary exosomal microRNAs in IgA nephropathyJournal of Clinical Laboratory Analysis, 2017
- Urinary exosomes as a novel biomarker for evaluation of α‐lipoic acid's protective effect in early diabetic nephropathyJournal of Clinical Laboratory Analysis, 2017
- MicroRNA as Biomarkers and DiagnosticsJournal of Cellular Physiology, 2015
- Exosomal ATF3 RNA Attenuates Pro‐Inflammatory Gene MCP‐1 Transcription in Renal Ischemia‐ReperfusionJournal of Cellular Physiology, 2014
- Exosome formation during maturation of mammalian and avian reticulocytes: Evidence that exosome release is a major route for externalization of obsolete membrane proteinsJournal of Cellular Physiology, 1991