微泡
小RNA
生物
脂肪组织
炎症
胰岛素抵抗
糖尿病
生物信息学
外体
能量稳态
癌症研究
疾病
葡萄糖稳态
基因表达调控
细胞生物学
免疫学
代谢组学
基因沉默
平衡
胰岛素
下调和上调
基因
内分泌系统
信号转导
计算生物学
核酸
核糖核酸
2型糖尿病
转录组
RNA干扰
代谢综合征
细胞
作者
Yong-Zhen Li,Yu Tao Zhang,Xiao Hong Li
出处
期刊:Cell Cycle
[Taylor & Francis]
日期:2025-11-17
卷期号:: 1-19
标识
DOI:10.1080/15384101.2025.2590058
摘要
Adipose tissue is central to energy homeostasis and endocrine function, and its dysregulation is a key driver of metabolic disorders. Exosomes, serving as critical intercellular messengers, mediate systemic metabolic responses by delivering bioactive cargo, including nucleic acids, proteins, and lipids. Mounting evidence identifies adipose-derived exosomes as potent mediators of obesity-related inflammation and glucose metabolic dysfunction, thereby contributing to insulin resistance and diabetic complications. This review summarizes the pivotal roles of exosomal microRNAs (miRNAs) and highlights their significant potential as a novel class of small RNA therapeutics. Unlike synthetic delivery systems, exosomal miRNAs constitute an inherent delivery vehicle that synergizes natural targeting efficiency with potent gene regulatory functions. This unique combination enables the precise coordination of complex gene networks involved in metabolic disease, offering a distinct advantage over conventional single-target approaches. Consequently, exosomal miRNAs are positioned as promising candidates for pioneering RNA-based therapies against pervasive conditions such as diabetes and cardiovascular disease.
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