The pathogenic, therapeutic and diagnostic role of exosomal microRNA in the autoimmune diseases

微泡 自身免疫 小RNA 自身免疫性疾病 免疫学 外体 免疫系统 多发性硬化 医学 发病机制 疾病 生物 抗体 基因 病理 遗传学
作者
Rasoul Mirzaei,Farhad Zamani,Marzieh Hajibaba,Ashkan Rasouli-Saravani,Mina Noroozbeygi,Melika Gorgani,Seyed Reza Hosseini‐Fard,Saba Jalalifar,Hossein Ajdarkosh,Seyed Hassnan Abedi,Hossein Keyvani,Sajad Karampoor
出处
期刊:Journal of Neuroimmunology [Elsevier]
卷期号:358: 577640-577640 被引量:75
标识
DOI:10.1016/j.jneuroim.2021.577640
摘要

Exosomes are a nano-vesicle surrounded by a bilipid layer that can release from almost all cells and could be detected in tissues and biological liquids. These vesicles contain lipids, proteins, and nucleic acids (including DNA, mRNA, and miRNA) inside and on the exosomes' surface constitute their content. Exosomes can transfer their cargo into the recipient cell, which can modify recipient cells' biological activities. Recently it has been deciphering that the miRNA pattern of exosomes reveals the cellular pathophysiological situation and modifies various biological processes. Increasing data regarding exosomes highlights that the exosomes and their cargo, especially miRNAs, are implicated in the pathophysiology of various disorders, such as autoimmune disease. The current evidence on the deciphering of mechanisms in which exosomal miRNAs contributed to autoimmunity was indicated that exosomal miRNA might hold information that can reprogram the function of many of the immune cells involved in autoimmune diseases' pathogenesis. In the present study, we summarized the pathogenic role of exosomal miRNAs in several autoimmune diseases, including myasthenia gravis (MG), psoriasis, inflammatory bowel disease (IBD), type 1 diabetes (T1D), multiple sclerosis (MS), systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), Sjogren's Syndrome (SS), systemic sclerosis (SSc), vitiligo, and autoimmune thyroid diseases (AITD). Moreover, in this work, we present evidence of the potential role of exosomal miRNAs as therapeutic and diagnostic agents in autoimmune diseases.
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