发病机制
小RNA
血管生成
骨质疏松症
血管内皮生长因子
生长因子
人口
骨重建
医学
血小板源性生长因子受体
癌症研究
生物
生物信息学
免疫学
内分泌学
内科学
血管内皮生长因子受体
遗传学
基因
受体
环境卫生
作者
Dailiang Zhang,Sheng Wang,Zunzhen Zhou,Limei Wang,Chongzhi Liu,Yuan Jiang
标识
DOI:10.3389/fendo.2024.1394785
摘要
Osteoporosis (OP) is a chronic systemic bone metabolism disease characterized by decreased bone mass, microarchitectural deterioration, and fragility fractures. With the demographic change caused by long lifespans and population aging, OP is a growing health problem. The role of miRNA in the pathogenesis of OP has also attracted widespread attention from scholars in recent years. Type H vessels are unique microvessels of the bone and have become a new focus in the pathogenesis of OP because they play an essential role in osteogenesis-angiogenesis coupling. Previous studies found some miRNAs regulate type H vessel formation through the regulatory factors, including platelet-derived growth factor-BB (PDGF-BB), hypoxia-inducible factor 1α (HIF-1α), vascular endothelial growth factor (VEGF), and so on. These findings help us gain a more in-depth understanding of the relationship among miRNAs, type H vessels, and OP to find a new perspective on treating OP. In the present mini-review, we will introduce the role of type H vessels in the pathogenesis of OP and the regulation of miRNAs on type H vessel formation by affecting regulatory factors to provide some valuable insights for future studies of OP treatment.
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