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血小板活化因子通过促进白细胞黏附在内皮细胞表面介导促凝血活性。

Platelet-activating factor mediates procoagulant activity on the surface of endothelial cells by promoting leukocyte adhesion.

作者信息

Lorant D E, Zimmerman G A, McIntyre T M, Prescott S M

机构信息

Nora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah School of Medicine, Salt Lake City, USA.

出版信息

Semin Cell Biol. 1995 Oct;6(5):295-303. doi: 10.1006/scel.1995.0039.

Abstract

Endothelial cells co-express platelet-activating factor and P-selectin on their surfaces after activation by certain receptor-mediated agonists. Together they mediate the adhesion of leukocytes to the endothelial cell surface. P-selectin tethers leukocytes to the endothelial cell surface allowing leukocyte activation by platelet-activating factor. Adhesion and activation are specific for leukocytes because they are the only cells known to express the ligand for P-selectin. Leukocytes adherent to the endothelial cell surface may promote thrombosis by three mechanisms: (1) they secrete factors that damage the underlying endothelium, (2) they secrete factors that directly initiate the coagulation cascade, and (3) they bind and activate platelets.

摘要

内皮细胞在被某些受体介导的激动剂激活后,会在其表面共表达血小板活化因子和P选择素。它们共同介导白细胞与内皮细胞表面的黏附。P选择素将白细胞束缚在内皮细胞表面,使白细胞能够被血小板活化因子激活。黏附和激活对白细胞具有特异性,因为它们是已知唯一表达P选择素配体的细胞。黏附在内皮细胞表面的白细胞可通过三种机制促进血栓形成:(1)它们分泌破坏下层内皮的因子;(2)它们分泌直接启动凝血级联反应的因子;(3)它们结合并激活血小板。

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