Wiebke J L, Montrose-Rafizadeh C, Zeitlin P L, Guggino W B
Department of Pediatrics, Johns Hopkins Medical Institutions, Baltimore, MD.
Biochim Biophys Acta. 1992 Mar 16;1134(2):105-11. doi: 10.1016/0167-4889(92)90033-8.
Endothelin-1 (ET-1), a peptide product of endothelial cells, is mitogenic for fibroblasts and smooth muscle cells. In this study we examined the effect of hypoxia on ET-1 production by bovine pulmonary vascular endothelial cells. Bovine pulmonary artery (BPAE) and microvascular endothelial (BMVE) cells were isolated, grown in tissue culture, and characterized by the presence of Factor VIII related antigen and LDL uptake. Baseline production of ET-1 by BPAE cells (measured by radioimmunoassay) increased over time. BMVE cells produced one tenth the amount of ET-1 as produced by the pulmonary artery endothelial cells under the same conditions. In both cell types, hypoxia (0% O2) significantly reduced the amount of ET-1 at 48 h. Restoration of normoxia in 21% O2 for 48 h resulted in a return of ET-1 levels to baseline. Northern blot analysis showed decreased ET-1 mRNA in cells exposed to hypoxia for 48 h. These data demonstrate that pulmonary vascular endothelial cells respond to hypoxia by reversibly decreasing ET-1 production, and this attenuation is likely regulated at the level of transcription.
内皮素 -1(ET -1)是内皮细胞产生的一种肽类产物,对成纤维细胞和平滑肌细胞具有促有丝分裂作用。在本研究中,我们检测了缺氧对牛肺血管内皮细胞产生ET -1的影响。分离牛肺动脉(BPAE)和微血管内皮(BMVE)细胞,在组织培养中生长,并通过存在因子VIII相关抗原和低密度脂蛋白摄取来进行鉴定。BPAE细胞的ET -1基础产量(通过放射免疫测定法测量)随时间增加。在相同条件下,BMVE细胞产生的ET -1量是肺动脉内皮细胞的十分之一。在两种细胞类型中,缺氧(0%氧气)在48小时时显著降低了ET -1的量。恢复到21%氧气的常氧环境48小时导致ET -1水平恢复到基线。Northern印迹分析显示,暴露于缺氧48小时的细胞中ET -1 mRNA减少。这些数据表明,肺血管内皮细胞通过可逆地减少ET -1产生来响应缺氧,并且这种衰减可能在转录水平受到调节。