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大鼠主动脉中的组织型纤溶酶原激活剂及其抑制剂。内毒素的影响。

Tissue-type plasminogen activator and its inhibitor in rat aorta. Effect of endotoxin.

作者信息

Padró T, Quax P H, van den Hoogen C M, Roholl P, Verheijen J H, Emeis J J

机构信息

Gaubius Laboratory TNO-PG, Leiden, Netherlands.

出版信息

Arterioscler Thromb. 1994 Sep;14(9):1459-65. doi: 10.1161/01.atv.14.9.1459.

Abstract

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.

摘要

对大鼠主动脉的三层结构进行纤溶酶原激活剂(PA)和PA抑制剂(PAI)的抗原、活性及mRNA分析,并研究内毒素对PA和PAI的影响。主动脉中的所有PA活性均被鉴定为组织型PA(TPA)活性;未检测到尿激酶型PA。在外膜层检测到TPA活性、TPA抗原和TPA mRNA,而在中膜层发现了TPA抗原和TPA mRNA,但未检测到TPA活性。在中膜层检测到PAI活性,这解释了该层中TPA活性缺失的原因。去除内皮细胞对内膜-中膜制剂中的TPA抗原和PAI活性没有影响。此外,无论内膜是否存在,在内膜-中膜制剂中发现的PAI-1 mRNA量相似。免疫组织化学染色显示,TPA免疫反应性存在于主动脉的所有三层结构中,而PAI-1免疫反应性存在于中膜平滑肌细胞中,而不存在于内皮细胞中。内毒素处理后,尽管TPA抗原和TPA mRNA未改变,但全主动脉和外膜提取物中的TPA活性降低。外膜层和中膜层的PAI-1 mRNA强烈增加,中膜层的PAI活性也增加。因此,内毒素通过增加PAI-1的合成降低了TPA活性;TPA未受影响。我们在大鼠主动脉中的观察结果与在小鼠主动脉和大鼠颈动脉中的观察结果不同,这提醒我们不要从一个组织(或物种)推断到另一个组织(或物种)。

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