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通过携带组织型纤溶酶原激活剂(tPA)的红细胞选择性溶解新生凝块进行预防性纤维蛋白溶解。

Prophylactic fibrinolysis through selective dissolution of nascent clots by tPA-carrying erythrocytes.

作者信息

Murciano Juan-Carlos, Medinilla Sandra, Eslin Donald, Atochina Elena, Cines Douglas B, Muzykantov Vladimir R

机构信息

Institute for Environmental Medicine, University of Pennsylvania, 3620 Hamilton Walk, Philadelphia, Pennsylvania 19104, USA.

出版信息

Nat Biotechnol. 2003 Aug;21(8):891-6. doi: 10.1038/nbt846. Epub 2003 Jul 6.

Abstract

A fibrinolytic agent consisting of a tissue-type plasminogen activator (tPA) coupled to the surface of red blood cells (RBCs) can dissolve nascent clots from within the clot, in a Trojan horse-like strategy, while having minimal effects on preexisting hemostatic clots or extravascular tissue. After intravenous injection, the fibrinolytic activity of RBC-tPA persisted in the bloodstream at least tenfold longer than did that of free tPA. In a model of venous thrombosis induced by intravenously injected fibrin microemboli aggregating in pulmonary vasculature, soluble tPA lysed pulmonary clots lodged before but not after tPA injection, whereas the converse was true for RBC-tPA. Free tPA failed to lyse occlusive carotid thrombosis whether injected before or after vascular trauma, whereas RBC-tPA circulating before, but not injected after, thrombus formation restored blood flow. This RBC-based drug delivery strategy alters the fibrinolytic profile of tPA, permitting prophylactic fibrinolysis.

摘要

一种由与红细胞(RBC)表面偶联的组织型纤溶酶原激活剂(tPA)组成的纤溶药物,能够以特洛伊木马策略从血栓内部溶解新生血栓,同时对已形成的止血血栓或血管外组织影响极小。静脉注射后,RBC - tPA的纤溶活性在血流中持续的时间比游离tPA至少长十倍。在静脉注射的纤维蛋白微栓子在肺血管系统中聚集诱导的静脉血栓形成模型中,可溶性tPA能溶解在tPA注射前而非注射后形成的肺血栓,而RBC - tPA则相反。无论在血管创伤前还是后注射,游离tPA都无法溶解闭塞性颈动脉血栓,而在血栓形成前循环但不在血栓形成后注射的RBC - tPA能恢复血流。这种基于红细胞的药物递送策略改变了tPA的纤溶特性,从而实现预防性纤溶。

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