Isolation, culture and identification of pulmonary arterial smooth muscle cells from rat distal pulmonary arteries

被引:24
作者
Peng, Gongyong [1 ]
Xu, Juan [1 ]
Liu, Rongmin [1 ]
Fu, Zhenli [1 ]
Li, Shaoxing [1 ,2 ]
Hong, Wei [3 ]
Chen, Jinglong [1 ]
Li, Bing [3 ]
Ran, Pixin [1 ]
机构
[1] Guangzhou Med Univ, Guangzhou Inst Resp Dis, Affiliated Hosp 1, State Key Lab Resp Dis, 151 Yanjiang Rd, Guangzhou 510120, Guangdong, Peoples R China
[2] Guangzhou Panyu Cent Hosp, Intens Care Unit, Guangzhou, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Res Ctr Expt Med, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Cell culture; Smooth muscle cells; Pulmonary artery; Rat; INTRACELLULAR CA2+ CONCENTRATION; ACUTE-HYPOXIA; UP-REGULATION; INDUCE APOPTOSIS; EXPRESSION; ENTRY; HYPERTENSION; PROLIFERATION; CHANNELS; SEROTONIN;
D O I
10.1007/s10616-017-0081-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 alpha-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.
引用
收藏
页码:831 / 840
页数:10
相关论文
共 44 条
[41]   VOLTAGE-GATED K+ CURRENTS REGULATE RESTING MEMBRANE-POTENTIAL AND [CA2+](I) IN PULMONARY ARTERIAL MYOCYTES [J].
YUAN, XJ .
CIRCULATION RESEARCH, 1995, 77 (02) :370-378
[42]   NO hyperpolarizes pulmonary artery smooth muscle cells and decreases the intracellular Ca2+ concentration by activating voltage-gated K+ channels [J].
Yuan, XJ ;
Tod, ML ;
Rubin, LJ ;
Blaustein, MP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (19) :10489-10494
[43]   Hypoxia inducible factor-1 mediates expression of miR-322: potential role in proliferation and migration of pulmonary arterial smooth muscle cells [J].
Zeng, Yan ;
Liu, Hongtao ;
Kang, Kang ;
Wang, Zhiwei ;
Hui, Gang ;
Zhang, Xiaoying ;
Zhong, Jiasheng ;
Peng, Wenda ;
Ramchandran, Ramaswamy ;
Raj, J. Usha ;
Gou, Deming .
SCIENTIFIC REPORTS, 2015, 5
[44]   Bone morphogenetic proteins induce apoptosis in human pulmonary vascular smooth muscle cells [J].
Zhang, S ;
Fantozzi, I ;
Tigno, DD ;
Yi, ES ;
Platoshyn, O ;
Thistlethwaite, PA ;
Kriett, JM ;
Yung, G ;
Rubin, LJ ;
Yuan, JXJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2003, 285 (03) :L740-L754