大鼠主动脉组织型纤溶酶原激活物及其抑制剂。内毒素的作用。

T Padró, P H Quax, C M van den Hoogen, P Roholl, J H Verheijen, J J Emeis
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引用次数: 27

摘要

分析三层大鼠主动脉纤溶酶原激活物(PA)和PAI的抗原、活性和mRNA,并研究内毒素对PA和PAI的影响。主动脉内所有PA活性均为组织型PA (TPA)活性;未检出尿激酶型PA。外膜中检测到TPA活性、TPA抗原和TPA mRNA,中膜中检测到TPA抗原和TPA mRNA,但未检测到TPA活性。在膜介质中检测到PAI活性,解释了在这一层中没有TPA活性。内皮细胞的去除对内膜-介质制备中的TPA抗原和PAI活性没有影响。此外,无论是否存在内膜,在内膜介质制备中均发现相似量的PAI-1 mRNA。免疫组化染色显示主动脉三层均有TPA免疫反应,而内侧平滑肌细胞有PAI-1免疫反应,内皮细胞无PAI-1免疫反应。内毒素处理后,总主动脉和外膜提取物中TPA活性降低,但TPA抗原和TPA mRNA不变。PAI-1 mRNA在外膜和中膜中显著升高,PAI活性在中膜中显著升高。因此,内毒素通过增加PAI-1的合成来降低TPA活性;TPA未受影响。我们对大鼠主动脉的观察结果与小鼠主动脉和大鼠颈动脉的观察结果不同,他们警告不要从一个组织(或物种)外推到另一个组织(或物种)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue-type plasminogen activator and its inhibitor in rat aorta. Effect of endotoxin.

Plasminogen activator (PA) and PA inhibitor (PAI) antigen, activity, and mRNA were analyzed in the three layers of rat aorta, and the effect of endotoxin on PA and PAI was studied. All PA activity in aorta was identified as tissue-type PA (TPA) activity; no urokinase-type PA was detected. In the tunica adventitia TPA activity, TPA antigen, and TPA mRNA were detected, whereas in the tunica media TPA antigen and TPA mRNA, but no TPA activity, were found. PAI activity was detected in the tunica media, explaining the absence of TPA activity in this layer. Removal of the endothelial cells had no effect on TPA antigen and PAI activity in intima-media preparations. Also, similar amounts of PAI-1 mRNA were found in intima-media preparations, irrespective of the presence or absence of the intima. Immunohistochemical staining showed that TPA immunoreactivity was present in all three layers of the aorta, whereas PAI-1 immunoreactivity was found in medial smooth muscle cells but not in endothelial cells. After endotoxin treatment, TPA activity was decreased in extracts of the total aorta and of the adventitia, although TPA antigen and TPA mRNA were unchanged. PAI-1 mRNA was strongly increased in the tunica adventitia and in the tunica media, as was PAI activity in the tunica media. Thus, endotoxin decreased TPA activity by increasing the synthesis of PAI-1; TPA was unaffected. Our observations in rat aorta differ from observations in mouse aorta and in rat carotid artery, and they caution against extrapolation from one tissue (or species) to another.

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