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血小板-中性粒细胞相互作用:连接止血与炎症

Platelet-neutrophil-interactions: linking hemostasis and inflammation.

作者信息

Zarbock Alexander, Polanowska-Grabowska Renata K, Ley Klaus

机构信息

Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia 22908-1394, USA.

出版信息

Blood Rev. 2007 Mar;21(2):99-111. doi: 10.1016/j.blre.2006.06.001. Epub 2006 Sep 20.

Abstract

Platelets are essential for primary hemostasis, but they also play an important pro-inflammatory role. Platelets normally circulate in a quiescent state. Upon activation, platelets can secrete and present various molecules, change their shape as well as the expression pattern of adhesion molecules. These changes are associated with the adhesion of platelets to leukocytes and the vessel wall. The interaction of platelets with neutrophils promotes the recruitment of neutrophils into inflammatory tissue and thus participates in host defense. This interaction of neutrophils with platelets is mainly mediated through P-selectin and beta(2) and beta(3) integrins (CD11b/CD18, CD41/CD61). Platelets can also interact with endothelial cells and monocytes. Adherent platelets promote the 'secondary capture' of neutrophils and other leukocytes. In addition, platelets secrete neutrophil and endothelial activators inducing production of inflammatory cytokines. Thus, platelets are important amplifiers of acute inflammation.

摘要

血小板对初级止血至关重要,但它们也发挥着重要的促炎作用。血小板通常以静止状态循环。激活后,血小板可分泌并呈递各种分子,改变其形状以及黏附分子的表达模式。这些变化与血小板与白细胞及血管壁的黏附有关。血小板与中性粒细胞的相互作用促进中性粒细胞募集至炎症组织,从而参与宿主防御。中性粒细胞与血小板的这种相互作用主要通过P-选择素以及β2和β3整合素(CD11b/CD18、CD41/CD61)介导。血小板还可与内皮细胞和单核细胞相互作用。黏附的血小板促进中性粒细胞和其他白细胞的“二次捕获”。此外,血小板分泌中性粒细胞和内皮激活剂,诱导炎症细胞因子的产生。因此,血小板是急性炎症的重要放大器。

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