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Unique subpopulations of CD56+ NK and NK-T peripheral blood lymphocytes identified by chemokine receptor expression repertoire.
Campbell, J J; Qin, S; Unutmaz, D; Soler, D; Murphy, K E; Hodge, M R; Wu, L; Butcher, E C.
Afiliação
  • Campbell JJ; Joint Program in Transfusion Medicine, Children's Hospital, 300 Longwood Avenue, Room BD-401, Boston, MA 02115. campbell_ja@tch.harvard.edu
J Immunol ; 166(11): 6477-82, 2001 Jun 01.
Article em En | MEDLINE | ID: mdl-11359797
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.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Matadoras Naturais / Subpopulações de Linfócitos T / Antígeno CD56 / Receptores de Quimiocinas Tipo de estudo: Prognostic_studies Limite: Adult / Humans Idioma: En Revista: J Immunol Ano de publicação: 2001 Tipo de documento: Article País de publicação: Estados Unidos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Matadoras Naturais / Subpopulações de Linfócitos T / Antígeno CD56 / Receptores de Quimiocinas Tipo de estudo: Prognostic_studies Limite: Adult / Humans Idioma: En Revista: J Immunol Ano de publicação: 2001 Tipo de documento: Article País de publicação: Estados Unidos