Trafficking of Th1 cells to lung - A role for selectins and a P-selectin glycoprotein-1-independent ligand

被引:18
作者
Clark, JG
Mandac-Dy, JB
Dixon, AE
Madtes, DK
Burkhart, KM
Harlan, JM
Bullard, DC
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[2] Univ Alabama Birmingham, Dept Genet, Birmingham, AL USA
[3] Univ Washington, Dept Med, Div Hematol, Seattle, WA 98195 USA
[4] Univ Washington, Div Pulm & Crit Care Med, Seattle, WA USA
关键词
D O I
10.1165/rcmb.2003-0208OC
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Trafficking of lymphocytes to lung is a critical component of pulmonary immune defense and surveillance. Selectins, expressed on vascular endothelium, regulate T lymphocyte emigration into tissues, such as skin, but the role of the selectins in trafficking of T cells to lung has not been well characterized. Here, we used a model of lung inflammation induced by adoptive transfer of alloreactive Th1 cells to analyze the role of P- and E-selectin in Th1 cell trafficking to lung in vivo. We found that both P- and E-selectin play an important role in Th1 lymphocyte migration to lung. We confirmed that the Th1 cells express P-selectin glycoprotein ligand-1, which was functional in binding to P- and E-selectin in vitro. However, our studies reveal that a ligand distinct from P-selectin glycoprotein-1 also binds these selectins in vitro and appears to play a physiologic role in in vivo emigration of Th1 lymphocytes into the lung.
引用
收藏
页码:220 / 227
页数:8
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