CD63 is an essential cofactor to leukocyte recruitment by endothelial P-selectin

被引:78
作者
Doyle, Emily L. [1 ,2 ,3 ]
Ridger, Victoria [4 ]
Ferraro, Francesco [1 ,2 ,3 ]
Turmaine, Mark [3 ]
Saftig, Paul [5 ]
Cutler, Daniel F. [1 ,2 ,3 ]
机构
[1] UCL, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
[2] UCL, MRC, Cell Biol Unit, London WC1E 6BT, England
[3] UCL, Dept Cell & Dev Biol, London WC1E 6BT, England
[4] Univ Sheffield, Dept Cardiovasc Sci, Fac Med Dent & Hlth, Sheffield, S Yorkshire, England
[5] Univ Kiel, Inst Biochem, D-2300 Kiel, Germany
基金
英国医学研究理事会;
关键词
WEIBEL-PALADE BODIES; TETRASPANIN-ENRICHED MICRODOMAINS; VON-WILLEBRAND-FACTOR; ROLLING IN-VIVO; CLATHRIN-COATED PITS; TUMOR-CELL MOTILITY; ACTIVATED PLATELETS; PROTEIN; ADHESION; FLOW;
D O I
10.1182/blood-2010-11-321489
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The activation of endothelial cells is critical to initiating an inflammatory response. Activation induces the fusion of Weibel-Palade Bodies (WPB) with the plasma membrane, thus transferring P-selectin and VWF to the cell surface, where they act in the recruitment of leukocytes and platelets, respectively. CD63 has long been an established component of WPB, but the functional significance of its presence within an organelle that acts in inflammation and hemostasis was unknown. We find that ablating CD63 expression leads to a loss of P-selectin-dependent function: CD63-deficient HUVECs fail to recruit leukocytes, CD63-deficient mice exhibit a significant reduction in both leukocyte rolling and recruitment and we show a failure of leukocyte extravasation in a peritonitis model. Loss of CD63 has a similar phenotype to loss of P-selectin itself, thus CD63 is an essential cofactor to P-selectin. (Blood. 2011;118(15):4265-4273)
引用
收藏
页码:4265 / 4273
页数:9
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