Xu J, Zhong N S
Guangzhou Respiratory Diseases Institute.
Zhonghua Jie He He Hu Xi Za Zhi. 1994 Jun;17(3):145-7, 189.
On the Co-culture model of pulmonary arterial endothelial cells (PECs) and smooth muscle cells (PSMCs), we studied the effects of hypoxia on the release of endothelin in cultured PECs and whether or not these effects could trigger the proliferation in PSMCs. Increase of the transcription of ET gene in cultured pulmonary arterial endothelial cells was shown when endothelial cells were exposed to hypoxia for 24h (95% N2 + 5% CO2, PO2 40-45mmHg in media), was showed to increase the transcription of ET gene in cultured pulmonary arterial endothelial cells by using situ hybridization method. The secretion of ET-1 from those cells into media by ET-1 radioimmunologic detection while 3HTdr incorporation in cultured PMCs was higher compared with normoxia, and administration of ETAb significantly reduced the increase of the incorporation in those compared with hypoxia alone. These results showed that exposure to hypoxia can promote ET-1 gene expression in PECs as well as release of ET from those cells, which of ET can stimulate DNA synthesis in cultured PMCs. It is suggested that enhanced ET release from PECs under hypoxia could stimulate PSMCs' proliferation which may induce pulmonary vessel remodeling--which may involve in the development of hypoxic pulmonary hypertension.
在肺动脉内皮细胞(PECs)和平滑肌细胞(PSMCs)的共培养模型上,我们研究了缺氧对培养的PECs中内皮素释放的影响,以及这些影响是否会引发PSMCs的增殖。当内皮细胞暴露于缺氧环境24小时(95% N2 + 5% CO2,培养基中PO2为40 - 45mmHg)时,通过原位杂交法显示培养的肺动脉内皮细胞中ET基因转录增加。通过ET - 1放射免疫检测发现这些细胞向培养基中分泌ET - 1,同时与常氧相比,培养的PSMCs中3HTdr掺入量更高,并且与单独缺氧相比,给予ETAb显著降低了掺入量的增加。这些结果表明,暴露于缺氧环境可促进PECs中ET - 1基因表达以及这些细胞释放ET,其中ET可刺激培养的PSMCs中的DNA合成。提示缺氧条件下PECs中ET释放增强可刺激PSMCs增殖,这可能诱导肺血管重塑——这可能参与了缺氧性肺动脉高压的发生发展。