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PMID: 11359797 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Unique subpopulations of CD56+ NK and NK-T peripheral blood lymphocytes identified by chemokine receptor expression repertoire.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 166 ·No. 11 ·2001-06-01 ·Pages 6477-82

Campbell JJ, Qin S, Unutmaz D, Soler D, Murphy KE, Hodge MR, Wu L, Butcher EC

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.

MeSH Terms
Adult CD56 Antigen/biosynthesis,blood Cell Movement/immunology Chemokines/blood,physiology Chemotaxis, Leukocyte/immunology Humans Immunophenotyping Killer Cells, Natural/metabolism,physiology Lymphoid Tissue/cytology,immunology Organ Specificity/immunology Receptors, Chemokine/biosynthesis,blood Receptors, IgG/biosynthesis,immunology T-Lymphocyte Subsets/metabolism,physiology
Chemicals
CD56 Antigen Chemokines Receptors, Chemokine Receptors, IgG
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Campbell J J
Joint Program in Transfusion Medicine, Children's Hospital, 300 Longwood Avenue, Room BD-401, Boston, MA 02115. campbell_ja@tch.harvard.edu
Qin S
Unutmaz D
Soler D
Murphy K E
Hodge M R
Wu L
Butcher E C
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2001-06-01
Pages
6477-82
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI37832 · United States
NIAID NIH HHS · AI46784 · United States
NIAID NIH HHS · AI47822 · United States
NIGMS NIH HHS · GM377342 · United States
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