发病机制
肺动脉高压
串扰
缺氧性肺血管收缩
细胞
病理
血管收缩
炎症
细胞生物学
医学
化学
免疫学
生物
心脏病学
内科学
物理
光学
生物化学
出处
期刊:Reviews of Physiology Biochemistry and Pharmacology
日期:2022-01-01
卷期号:: 159-179
被引量:3
摘要
Pulmonary hypertension (PH) is a disease with high pulmonary arterial pressure, pulmonary vasoconstriction, pulmonary vascular remodeling, and microthrombosis in complex plexiform lesions, but it has been unclear of the exact mechanism of PH. A new understanding of the pathogenesis of PH is occurred and focused on the role of crosstalk between the cells on pulmonary vessels and pulmonary alveoli. It was found that the crosstalks among the endothelial cells, smooth muscle cells, fibroblasts, pericytes, alveolar epithelial cells, and macrophages play important roles in cell proliferation, migration, inflammation, and so on. Therefore, the heterogeneity of multiple pulmonary blood vessels and alveolar cells and tracking the transmitters of cell communication could be conducive to the further insights into the pathogenesis of PH to discover the potential therapeutic targets for PH.
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