Publikationsdatum:
2004-11-13
Beschreibung:
NKT cells represent a distinct lineage of T cells that coexpress a conserved alphabeta T cell receptor (TCR) and natural killer (NK) receptors. Although the TCR of NKT cells is characteristically autoreactive to CD1d, a lipid-presenting molecule, endogenous ligands for these cells have not been identified. We show that a lysosomal glycosphingolipid of previously unknown function, isoglobotrihexosylceramide (iGb3), is recognized both by mouse and human NKT cells. Impaired generation of lysosomal iGb3 in mice lacking beta-hexosaminidase b results in severe NKT cell deficiency, suggesting that this lipid also mediates development of NKT cells in the mouse. We suggest that expression of iGb3 in peripheral tissues may be involved in controlling NKT cell responses to infections and malignancy and in autoimmunity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhou, Dapeng -- Mattner, Jochen -- Cantu, Carlos 3rd -- Schrantz, Nicolas -- Yin, Ning -- Gao, Ying -- Sagiv, Yuval -- Hudspeth, Kelly -- Wu, Yun-Ping -- Yamashita, Tadashi -- Teneberg, Susann -- Wang, Dacheng -- Proia, Richard L -- Levery, Steven B -- Savage, Paul B -- Teyton, Luc -- Bendelac, Albert -- AI053725/AI/NIAID NIH HHS/ -- AI50847/AI/NIAID NIH HHS/ -- P20RR16459/RR/NCRR NIH HHS/ -- R01 AI38339/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Dec 3;306(5702):1786-9. Epub 2004 Nov 11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉University of Chicago, Department of Pathology, Chicago, IL 60637, USA. dzhou@midway.uchicago.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15539565" target="_blank"〉PubMed〈/a〉
Schlagwort(e):
Animals
;
Antigen Presentation
;
Antigens, CD1/immunology/metabolism
;
Antigens, CD1d
;
Autoimmunity
;
Cell Line
;
Cell Line, Tumor
;
Cells, Cultured
;
Dendritic Cells/immunology
;
Galactosyltransferases/genetics/metabolism
;
Globosides/chemistry/*immunology/metabolism
;
Humans
;
Hybridomas
;
Infection/immunology
;
Killer Cells, Natural/*immunology
;
Ligands
;
Lymphocyte Activation
;
Lymphocyte Count
;
Lysosomes/*metabolism
;
Mice
;
Mice, Inbred C57BL
;
Neoplasms/immunology
;
Plant Lectins/immunology
;
Rats
;
Receptors, Antigen, T-Cell, alpha-beta/immunology
;
Saposins/metabolism
;
T-Lymphocyte Subsets/*immunology
;
beta-N-Acetylhexosaminidases/genetics/metabolism
Print ISSN:
0036-8075
Digitale ISSN:
1095-9203
Thema:
Biologie
,
Chemie und Pharmazie
,
Informatik
,
Medizin
,
Allgemeine Naturwissenschaft
,
Physik
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