微泡
医学
衰老
疾病
细胞外小泡
内皮功能障碍
糖尿病
胞外囊泡
平衡
表观遗传学
小RNA
内皮干细胞
机制(生物学)
生物信息学
氧化应激
内皮
细胞生物学
免疫学
病理
生物
内科学
内分泌学
体外
基因
认识论
生物化学
哲学
作者
Julia Carracedo,Matilde Alique,Rafael Ramírez-Carracedo,Guillermo Bodega,Rafael Ramı́rez
出处
期刊:Current Vascular Pharmacology
[Bentham Science]
日期:2019-08-01
卷期号:17 (5): 447-454
被引量:26
标识
DOI:10.2174/1570161116666180820115726
摘要
Endothelial senescence-associated with aging or induced prematurely in pathological situations, such as diabetes, is a first step in the development of Cardiovascular Disease (CVDs) and particularly inflammatory cardiovascular diseases. The main mechanism that links endothelial senescence and the progression of CVDs is the production of altered Extracellular Vesicles (EVs) by senescent endothelial cells among them, Microvesicles (MVs). MVs are recognized as intercellular signaling elements that play a key role in regulating tissue homeostasis. However, MVs produced by damage cell conveyed epigenetic signals, mainly involving microRNAs, which induce many of the injured responses in other vascular cells leading to the development of CVDs. Many studies strongly support that the quantification and characterization of the MVs released by senescent endothelial cells may be useful diagnostic tools in patients with CVDs, as well as a future therapeutic target for these diseases. In this review, we summarize the current knowledge linking senescence-associated MVs to the development of CVDs and discuss the roles of these MVs, in particular, in diabetic-associated increases the risk of CVDs.
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