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大鼠组织血管中内源性抗凝血酶III的免疫细胞化学定位揭示了具有抗凝活性的硫酸乙酰肝素蛋白聚糖的位置。

Immunocytochemical localization of endogenous anti-thrombin III in the vasculature of rat tissues reveals locations of anticoagulantly active heparan sulfate proteoglycans.

作者信息

Xu Y, Slayter H S

机构信息

Laboratory of Electron Microscopy, Dana Farber Cancer Institute, Boston, Massachusetts 02115.

出版信息

J Histochem Cytochem. 1994 Oct;42(10):1365-76. doi: 10.1177/42.10.7930519.

Abstract

We localized endogenous anti-thrombin III (ATIII) by light and electron microscopic immunocytochemical staining in cryostat and ultra-thin frozen sections of 10 different rat tissues, using rabbit alpha-human ATIII antibody that was shown to crossreact strongly with rat ATIII. EM immunocytochemical methods revealed discrete deposits of endogenous ATIII (absent after heparinase treatment), and thus by inference anticoagulantly active heparan sulfate proteoglycans (HSPGs) at a resolution of 10-20 nm, or an order of magnitude better than autoradiography or LM. ATIII was found in variable amounts almost entirely in the subendothelial space of blood vessels in various rat tissues. In kidney, ATIII was found immediately beneath the endothelium, in concentrated clusters associated with the vascular basement membrane. Equally important is the observed variation in expression of ATIII in the various tissues studied (i.e., kidney > liver, aorta, lung, spleen, adrenal > intestine, muscle, brain). On the basis of these observations, we confirm a model in which vascular abluminal and, perhaps to a much smaller extent, luminal anticoagulantly active HSPGs regulate coagulation mechanism activity, either by serving as a reserve of anticoagulant or by modulating the ambient function of the coagulation cascade.

摘要

我们使用兔抗人α-抗凝血酶III(ATIII)抗体,通过光镜和电镜免疫细胞化学染色法,对10种不同大鼠组织的低温恒温器切片和超薄冷冻切片中的内源性抗凝血酶III(ATIII)进行了定位。该抗体已被证明与大鼠ATIII有强烈的交叉反应。电镜免疫细胞化学方法揭示了内源性ATIII的离散沉积物(肝素酶处理后消失),从而推断出抗凝活性硫酸乙酰肝素蛋白聚糖(HSPGs)的分辨率为10-20纳米,比放射自显影或光镜观察要好一个数量级。在各种大鼠组织中,几乎在血管内皮下空间中发现了数量不等的ATIII。在肾脏中,ATIII立即在内皮下方被发现,集中成簇与血管基底膜相关。同样重要的是,在所研究的各种组织中观察到的ATIII表达差异(即肾脏>肝脏、主动脉、肺、脾脏、肾上腺>肠道、肌肉、大脑)。基于这些观察结果,我们证实了一种模型,即血管腔外,或许在更小程度上血管腔内的抗凝活性HSPGs通过作为抗凝储备或调节凝血级联反应的周围功能来调节凝血机制活性。

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