在流动状态下,血小板与单核细胞的结合优先于与中性粒细胞的结合。

Preferential binding of platelets to monocytes over neutrophils under flow.

作者信息

Ahn Kyung C, Jun Andy J, Pawar Parag, Jadhav Sameer, Napier Susan, McCarty Owen J T, Konstantopoulos Konstantinos

机构信息

Department of Chemical and Biomolecular Engineering, The Johns Hopkins University, Baltimore, MD 21218, USA.

出版信息

Biochem Biophys Res Commun. 2005 Apr 1;329(1):345-55. doi: 10.1016/j.bbrc.2005.01.146.

Abstract

This study was undertaken to systematically investigate the binding kinetics of platelet recruitment by monocytes relative to neutrophils in bulk suspensions subjected to shear as well as the molecular requirements of leukocyte-platelet binding. Hydrodynamic shear-induced collisions augment the proportion of monocytes with adherent platelets more drastically than that of neutrophils with bound platelets. These heterotypic interactions are further potentiated by platelet activation with thrombin or to a lesser extent by monocyte stimulation with N-formyl-methionyl-leucyl-phenylalanine (fMLP). Monocyte-platelet heteroaggregation increases with increasing shear rate and shear exposure time. Platelet P-selectin binding to monocyte P-selectin-glycoprotein-ligand-1 is solely responsible for maximal platelet adhesion to unstimulated monocytes in shear flow. However, the enhanced platelet binding to fMLP-treated monocytes involves a sequential two-step process, wherein P-selectin-PSGL-1 interactions are stabilized by CD18-integrin involvement. Blocking platelet alpha(IIb)beta(3) or monocyte beta(1)-integrin function had no effect. This study underscores the preferential recruitment of platelets by monocytes relative to neutrophils in shear flow, and demonstrates that the shear environment of the vasculature coupled to the state of cell activation modulates the dynamics and molecular constituents mediating monocyte-platelet adhesion.

摘要

本研究旨在系统地研究在受到剪切力的大量悬浮液中,单核细胞相对于中性粒细胞募集血小板的结合动力学,以及白细胞与血小板结合的分子要求。流体动力剪切诱导的碰撞比中性粒细胞与结合血小板的碰撞更显著地增加了单核细胞与黏附血小板的比例。血小板用凝血酶激活或单核细胞用N-甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)刺激在较小程度上可进一步增强这些异型相互作用。单核细胞-血小板异聚体随着剪切速率和剪切暴露时间的增加而增加。在剪切流中,血小板P-选择素与单核细胞P-选择素糖蛋白配体-1的结合是血小板最大程度黏附于未刺激单核细胞的唯一原因。然而,血小板与fMLP处理的单核细胞结合增强涉及一个连续的两步过程,其中P-选择素-PSGL-1相互作用通过CD18整合素的参与而稳定。阻断血小板α(IIb)β(3)或单核细胞β1整合素功能没有影响。本研究强调了在剪切流中单核细胞相对于中性粒细胞对血小板的优先募集,并表明血管系统的剪切环境与细胞激活状态共同调节介导单核细胞-血小板黏附的动力学和分子成分。

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