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牛玻璃体和房水中纤溶活性及纤溶酶原激活物的定位

Fibrinolytic activity and localization of plasminogen activator in bovine vitreous body and aqueous humor.

作者信息

Hayashi K, Nakashima Y, Sueishi K, Tanaka K

机构信息

Department of Pathology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Jpn J Ophthalmol. 1989;33(1):66-75.

PMID:2499726
Abstract

The types, activities and concentrations of plasminogen activator (PA) were examined in the bovine vitreous body and aqueous humor. Molecular weights of PA in the vitreous body and aqueous humor were approximately 66 and 110 kilodaltons (kDa), respectively, as determined by fibrinolysis enzymography. These PA activities were neutralized by anti-human tissue PA (t-PA) IgG but not by anti-human urokinase PA (u-PA) IgG. Both findings indicated that the main PA in the vitreous body and aqueous humor is t-PA. The existence of u-PA could not be confirmed in intraocular fluids. Fibrinolytic activities measured by amidolytic assay were 0.12 +/- 0.01 IU/ml in the vitreous body and 0.04 +/- 0.02 IU/ml in the aqueous humor. High concentrations but relatively low fibrinolytic activities suggested that PA and PA inhibitor coexisted in the intraocular fluids. Moreover, unbound PA inhibitor was not detected by reverse fibrinolysis enzymography. The present study suggests that most of the PA inhibitor combines with PA and forms a complex. PA predominates over PA inhibitor in the intraocular fluids, whereas PA inhibitor predominates in the plasma. The results by Todd's fibrinolysis autography and immunohistochemical staining showed that t-PA was present in the corneal endothelial cells, which are in direct contact with the aqueous humor. This suggests that not only the vascular system but the corneal endothelial cells as well might be a source of the PA of the aqueous humor and possibly of the vitreous body also.

摘要

对牛玻璃体和房水中纤溶酶原激活剂(PA)的类型、活性及浓度进行了检测。通过纤维蛋白溶解酶谱法测定,玻璃体和房水中PA的分子量分别约为66千道尔顿(kDa)和110千道尔顿(kDa)。这些PA活性可被抗人组织型PA(t-PA)IgG中和,但不能被抗人尿激酶型PA(u-PA)IgG中和。这两个结果均表明,玻璃体和房水中的主要PA是t-PA。在眼内液中未证实存在u-PA。通过酰胺分解测定法测得的纤维蛋白溶解活性在玻璃体中为0.12±0.01 IU/ml,在房水中为0.04±0.02 IU/ml。高浓度但相对较低的纤维蛋白溶解活性表明PA和PA抑制剂共存于眼内液中。此外,通过反向纤维蛋白溶解酶谱法未检测到未结合的PA抑制剂。本研究表明,大多数PA抑制剂与PA结合并形成复合物。在眼内液中PA占主导地位,而在血浆中PA抑制剂占主导地位。Todd纤维蛋白溶解自显影和免疫组织化学染色结果显示,t-PA存在于与房水直接接触的角膜内皮细胞中。这表明不仅血管系统,角膜内皮细胞也可能是房水以及可能还有玻璃体中PA的来源。

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