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胎盘硫酸皮肤素:分离、抗凝活性及其与肝素辅因子II的关联。

Placental dermatan sulfate: isolation, anticoagulant activity, and association with heparin cofactor II.

作者信息

Giri Tusar K, Tollefsen Douglas M

机构信息

Hematology Division, Campus Box 8125, Washington University Medical School, 660 South Euclid Ave, St Louis, MO 63110, USA.

出版信息

Blood. 2006 Apr 1;107(7):2753-8. doi: 10.1182/blood-2005-09-3755. Epub 2005 Dec 8.

Abstract

Pregnancy is associated with hemostatic challenges that may lead to thrombosis. Heparin cofactor II (HCII) is a glycosaminoglycan-dependent thrombin inhibitor present in both maternal and fetal plasma. HCII activity increases during pregnancy, and HCII levels are significantly decreased in women with severe pre-eclampsia. Dermatan sulfate (DS) specifically activates HCII and is abundant in the placenta, but the locations of DS and HCII in the placenta have not been determined. We present evidence that DS is the major anticoagulant glycosaminoglycan in the human placenta at term. DS isolated from human placenta contains disaccharides implicated in activation of HCII and has anticoagulant activity similar to that of mucosal DS. Immunohistochemical studies revealed that DS is associated with fetal blood vessels and stromal regions of placental villi but is notably absent from the syncytiotrophoblast cells in contact with the maternal circulation. HCII colocalizes with DS in the walls of fetal blood vessels and is also present in syncytiotrophoblast cells. Our data suggest that DS is in a position to activate HCII in the fetal blood vessels or in the stroma of placental villi after injury to the syncytiotrophoblast layer and thereby inhibit fibrin generation in the placenta.

摘要

妊娠与可能导致血栓形成的止血挑战相关。肝素辅因子II(HCII)是一种存在于母体和胎儿血浆中的糖胺聚糖依赖性凝血酶抑制剂。妊娠期间HCII活性增加,而重度子痫前期女性的HCII水平显著降低。硫酸皮肤素(DS)可特异性激活HCII,且在胎盘中含量丰富,但DS和HCII在胎盘中的位置尚未确定。我们提供的证据表明,足月时DS是人类胎盘中主要的抗凝糖胺聚糖。从人胎盘中分离出的DS含有与HCII激活有关的二糖,并且具有与粘膜DS相似的抗凝活性。免疫组织化学研究显示,DS与胎盘绒毛的胎儿血管和基质区域相关,但与母体循环接触的合体滋养层细胞中明显不存在。HCII与DS在胎儿血管壁中共定位,并且也存在于合体滋养层细胞中。我们的数据表明,在合体滋养层受损后,DS能够在胎儿血管或胎盘绒毛基质中激活HCII,从而抑制胎盘中纤维蛋白的生成。

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