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低氧对培养的不同内径的肺动脉平滑肌细胞增殖的影响
作者姓名:Yu TZ  Ma CT
作者单位:湖南医科大学心血管生理研究室,
摘    要:目的和方法:分离培养三种不同内径的肺动脉平滑肌细胞(PASMCs),用^3H-TdR掺入速率和细胞计数作为细胞增殖的指标,观察低氧对其增殖作用的影响。结果:低氧对三种不同内径的PASMCs(内径分别为>1000μm、500-800μm、300-400μm)增殖促进作用显著不同,其^3H-TdR掺入速率和细胞计数分别增加23.5%和11.1%、60.0%和33.8%、141.4%和52.0%,选择对低氧最敏感的PASMCs(内径为300-400μm),进一步探讨低氧促PASMCs增殖作用的细胞机制:钙拮抗剂verapail、蛋白激酶C抑制剂staurosporine(Stau)和细胞Na-H交换抑制剂amiloride可显著降低低氧情况下PASMCs^3H-TdR掺入速率和细胞计数。结论:低氧对三种不同内径的PASMCs增殖促进作用显著不同; Ca^2 、蛋白激酶C和Na^2 -H^ 交换的激活,可能是低氧促PASMCs增殖的重要胞内信息转导机制。

关 键 词:低氧  肺动脉平滑肌细胞  增殖  信息转导
文章编号:1000-6834(2001)01-0058-03
修稿时间:1999年5月7日

Effects of hypoxia on proliferation of pulmonary arterial smooth muscle cells
Yu TZ,Ma CT.Effects of hypoxia on proliferation of pulmonary arterial smooth muscle cells[J].Chinese Journal of Applied Physiology,2001,17(1):58-60.
Authors:Yu T Z  Ma C T
Institution:Laboratory of Cardiovascular Physiology, Hunan Medical University, Changsha 410078.
Abstract:To investigate the effects of hypoxia on the prolifera tion of different diameter intra-pulmonary artery smooth muscle cells(PASMCs) ,and to study the possible signal transduction pathway in proliferation caused b y hypoxia. Methods: PASMCs were isola-ted from three different size of pulmonary arteries (>1 000 μm. 500~800 μm. 300~400 μm diameter) and cultured separetely.3H-TdR incorporation and cell number were used to measur e cell proliferation. Results:3H-TdR incorporation and cell numbe r of PASMCs from three sizes of pulmonary artery (>1 000 μm, 500~800μm, 800~ 400 μm diameter) increased 23. 5% and 11.1%, 60.0% and 33.8%, 141.4% and 52 .0%, respe ctively. Calcium antagonist (verapail) , PKC inhibitor (staurosporine), and Na +-H+ exchange inhibitor (amiloride) were used in PASMCs isolated from 300~40 0 μm diameter pulmonary artery. The results showed that verapail, stauroporine and amiloride could notably block hypoxia -induced increase 3 H -TdR incorporation and cell number. Conclusion: Proliferation of pu lmonary artery smooth muscle cell responded to hypoxia differently according to the artery size; activation of calcium channel, PKC and Na+-H+ exchange mig ht mediate the proliferation initiated by hypoxia.
Keywords:hypoxia  pulmonary artery smooth muscle  hyperplasia  messenger transduction
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