Rules of Recruitment for Th1 and Th2 Lymphocytes in Inflamed Liver: A Role for Alpha-4 Integrin and Vascular Adhesion Protein-1

The mechanisms that mediate the recruitment of Th1 and Th2 lymphocytes in vivo are poorly understood. We demonstrate that the mechanisms by which exogenously produced CD4 + Th1 and Th2 cells roll and adhere in Con A-inflamed liver microcirculation differ dramatically: Th1 cells use α 4β 1-integrin a...

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Published in:Immunity (Cambridge, Mass.) Vol. 23; no. 2; pp. 153 - 163
Main Authors: Bonder, Claudine S., Norman, M. Ursula, Swain, Mark G., Zbytnuik, Lori D., Yamanouchi, Jun, Santamaria, Pere, Ajuebor, Maureen, Salmi, Marko, Jalkanen, Sirpa, Kubes, Paul
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01-08-2005
Elsevier Limited
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Summary:The mechanisms that mediate the recruitment of Th1 and Th2 lymphocytes in vivo are poorly understood. We demonstrate that the mechanisms by which exogenously produced CD4 + Th1 and Th2 cells roll and adhere in Con A-inflamed liver microcirculation differ dramatically: Th1 cells use α 4β 1-integrin and Th2 cells use the vascular adhesion protein (VAP)-1. P-selectin plays no detectable role in Th1 or Th2 cell trafficking in liver microcirculation. Cellular recruitment in the liver sinusoids has previously been shown to be independent of many known adhesion molecules, leading to the suggestion that recruitment in these structures is mediated by physical trapping. While this may still be true for neutrophils, Th1 and Th2 cells use α 4-integrin and VAP-1, respectively, to adhere within the liver sinusoids.
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ISSN:1074-7613
1097-4180
DOI:10.1016/j.immuni.2005.06.007