| Literature DB >> 28321780 |
Gongyong Peng1, Juan Xu2, Rongmin Liu2, Zhenli Fu2, Shaoxing Li2,3, Wei Hong4, Jinglong Chen2, Bing Li4, Pixin Ran5.
Abstract
The culture of pulmonary arterial smooth muscle cells (PASMCs) is one of the most powerful tools for exploring the mechanisms of pulmonary hypertension (PH). Both pulmonary vasoconstriction and remodeling occur predominantly in distal pulmonary arteries (PA). In this study, we provide our detailed and standardized protocol for easy isolation and culture of PASMCs from rat distal PA to supply every investigator with a simple, economical and useful method in studying PH. The protocol can be divided into four stages: isolation of distal PA, isolation of cells, growth in culture and passage of cells. Rat distal PASMCs were characterized by morphological activity and by immunostaining for smooth muscle α-actin and smooth muscle myosin heavy chain, but not for CD90/Thy-1 or von Willebrand factor. Furthermore, functional assessments were performed, confirming the presence of voltage-dependent Ca2+ channels and physiological characteristic of response to hypoxia. In conclusion, we have developed a detailed and simple protocol for obtaining rat distal PASMCs. These PASMCs exhibit features consistent with vascular smooth muscle cells, and they could subsequently be used to further explore the pathophysiological mechanisms of PH.Entities:
Keywords: Cell culture; Pulmonary artery; Rat; Smooth muscle cells
Year: 2017 PMID: 28321780 PMCID: PMC5595745 DOI: 10.1007/s10616-017-0081-8
Source DB: PubMed Journal: Cytotechnology ISSN: 0920-9069 Impact factor: 2.058