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The Journal of Immunology, 1999, 162: 4914-4919.
Copyright © 1999 by The American Association of Immunologists

A Circulating Bovine {gamma}{delta} T Cell Subset, Which Is Found in Large Numbers in the Spleen, Accumulates Inefficiently in an Artificial Site of Inflammation: Correlation with Lack of Expression of E-Selectin Ligands and L-Selectin1

Eric Wilson, M. Kemal Aydintug and Mark A. Jutila2

Department of Veterinary Molecular Biology, Montana State University, Bozeman, MT 59717

Tissue-specific localization of TCR-defined subsets of {gamma}{delta} T cells has been widely reported; however, the mechanisms responsible for this phenomenon are poorly understood. We describe a bovine {gamma}{delta} T cell TCR-associated subset that preferentially localizes in the spleen. This subset was characterized by coexpression of CD8, and was found to lack surface expression of E-selectin ligands, GR Ag ligands, as well as low expression of L-selectin. The CD8-positive {gamma}{delta} T cell subset did not accumulate at sites of inflammation as efficiently as CD8-negative {gamma}{delta} T cells that, in contrast, express E-selectin and GR ligands and high levels of L-selectin. This is the first demonstration of a {gamma}{delta} T cell subset, which exhibits a defined tissue tropism, having a unique adhesion molecule expression profile. These results demonstrate that in some cases tissue-specific accumulation of {gamma}{delta} T cell subsets can be predicted by expression, or lack of expression, of defined homing molecules.




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