Laug W E
Thromb Haemost. 1983 Dec 30;50(4):888-92.
Confluent cultures of bovine aortic endothelial cells (BEC) were found to secrete both tissue type plasminogen activator (t-PA) and urokinase type plasminogen activator (u-PA). Exposure of the cultures to increasing concentrations of dexamethasone resulted in a time and concentration dependent inhibition of cellular and secreted u-PA. Complete inhibition of u-PA production and secretion was found at dexamethasone concentrations of 10(-8) molar or higher. Several distinct PA forms with molecular weights ranging from 10,000-20,000 to greater than 200,000 were found in the conditioned medium of untreated BEC cultures. After addition of dexamethasone (10(-7) molar) to the culture medium the PAs with molecular weights of 117,000, 58,000, 47,000, were absent suggesting that they were u-PAs, whereas the PAs with molecular weights of greater than 200,000 and 75,000 remained unchanged suggesting their t-PA origins. The PAs with lower molecular weights of 35,000, 28,000 and 10,000 to 20,000 were most likely generated from the higher molecular weight forms by limited proteolysis since they were absent when the medium was conditioned in the presence of the protease inhibitor Trasylol. The two PA types may therefore be independently regulated in BEC.
研究发现,牛主动脉内皮细胞(BEC)的融合培养物可分泌组织型纤溶酶原激活物(t-PA)和尿激酶型纤溶酶原激活物(u-PA)。将培养物暴露于浓度不断增加的地塞米松中,会导致细胞和分泌型u-PA受到时间和浓度依赖性抑制。在地塞米松浓度为10^(-8)摩尔或更高时,发现u-PA的产生和分泌被完全抑制。在未处理的BEC培养物的条件培养基中发现了几种不同形式的PA,其分子量范围从10,000 - 20,000到大于200,000。向培养基中添加地塞米松(10^(-7)摩尔)后,分子量为117,000、58,000、47,000的PA消失,表明它们是u-PA,而分子量大于200,000和75,000的PA保持不变,表明它们起源于t-PA。分子量较低的35,000、28,000以及10,000 - 20,000的PA很可能是由较高分子量形式通过有限的蛋白水解产生的,因为当培养基在蛋白酶抑制剂抑肽酶存在的情况下进行条件培养时,它们不存在。因此,这两种PA类型在BEC中可能受到独立调节。