Abstract

Pulmonary arterial hypertension (PAH) is a disease of unknown etiology that leads to a progressive increase in pulmonary vascular resistance (PVR), if untreated, ultimately right heart failure and high mortality.It is concerted pulmonary vascular contraction and vascular remodeling are the 2 main courses of physiology and pathology leading to PAH, especially the significant role of proliferation of pulmonary arterial smooth muscle cells.A lot of relevant factors are revealed to take a participation into regulating the proliferation of pulmonary arterial smooth muscle cells and finally PAH. Key words: Pulmonary arterial smooth muscle cell; Cell proliferation; Relevant factor; Pulmonary arterial hypertension

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