Unique Subpopulations of CD56+ NK and NK-T Peripheral Blood Lymphocytes Identified by Chemokine Receptor Expression Repertoire

James J. Campbell(Boston Children's Hospital), Shixin Qin(Millennium Engineering and Integration (United States)), Derya Unutmaz(Vanderbilt University), Dulce Soler(Millennium Engineering and Integration (United States)), Kristine Murphy(Millennium Engineering and Integration (United States)), Martin R. Hodge(Millennium Engineering and Integration (United States)), Lijun Wu(Millennium Engineering and Integration (United States)), Eugene C. Butcher(VA Palo Alto Health Care System)
The Journal of Immunology
June 1, 2001
Cited by 511Open Access
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Abstract

CD56, an adhesion molecule closely related to neural cell adhesion molecule, is an immunophenotypic marker for several unique populations of PBLS: Although CD56(+) cells derive from multiple lymphocyte lineages, they share a role in immunosurveillance and antitumor responses. We have studied the chemokine receptor expression patterns and functional migratory responses of three distinct CD56(+) populations from human peripheral blood. NK-T cells were found to differ greatly from NK cells, and CD16(+) NK cells from CD16(-) NK cells. CD16(+) NK cells were the predominant population responding to IL-8 and fractalkine, whereas NK-T cells were the predominant population responding to the CCR5 ligand macrophage-inflammatory protein-1beta. CD16(-) NK cells were the only CD56(+) population that uniformly expressed trafficking molecules necessary for homing into secondary lymphoid organs through high endothelial venule. These findings describe a diverse population of cells that may have trafficking patterns entirely different from each other, and from other lymphocyte types.


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