Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2000-8-3
pubmed:abstractText
We recently reported that the number of gamma delta T cells was increased after infection with Escherichia coli in C3H/HeN mice. We here showed that an i.p. injection with native lipid A derived from E. coli induced an increase of gamma delta T cells in the peritoneal cavity of LPS-responsive C3H/HeN mice and, albeit to a lesser degree, also in LPS-hyporesponsive C3H/HeJ mice. The purified gamma delta T cells from C3H/HeN and C3H/HeJ mice expressed a canonical TCR repertoire encoded by V gamma 6-J gamma 1/V delta 1-D delta 2-J delta 2 gene segments and proliferated in response to the native lipid A derived from E. coli in a TCR-independent manner. The lipid A-reactive gamma delta T cells bearing canonical V gamma 6/V delta 1 expressed Toll-like receptor (TLR) 2 mRNA, while TLR4 mRNA was undetectable. Treatment with a TLR2 anti-sense oligonucleotide resulted in hyporesponsiveness of the gamma delta T cells to the native lipid A. TLR2-deficient mice showed an impaired increase of the gamma delta T cells following injection of native lipid A. These results suggest that TLR2 is involved in the activation of canonical V gamma 6/V delta 1 T cells by native E. coli lipid A.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD14, http://linkedlifedata.com/resource/pubmed/chemical/Cytokines, http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Lipid A, http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell..., http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface, http://linkedlifedata.com/resource/pubmed/chemical/Toll-Like Receptor 2, http://linkedlifedata.com/resource/pubmed/chemical/Toll-Like Receptor 4, http://linkedlifedata.com/resource/pubmed/chemical/Toll-Like Receptors
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
165
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
931-40
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10878368-Animals, pubmed-meshheading:10878368-Antigens, CD14, pubmed-meshheading:10878368-Ascitic Fluid, pubmed-meshheading:10878368-Cell Line, pubmed-meshheading:10878368-Cytokines, pubmed-meshheading:10878368-Drosophila Proteins, pubmed-meshheading:10878368-Escherichia coli Infections, pubmed-meshheading:10878368-Female, pubmed-meshheading:10878368-Gene Expression Regulation, pubmed-meshheading:10878368-Genes, T-Cell Receptor delta, pubmed-meshheading:10878368-Genes, T-Cell Receptor gamma, pubmed-meshheading:10878368-Injections, Intraperitoneal, pubmed-meshheading:10878368-Lipid A, pubmed-meshheading:10878368-Lipopolysaccharides, pubmed-meshheading:10878368-Lymphocyte Activation, pubmed-meshheading:10878368-Membrane Glycoproteins, pubmed-meshheading:10878368-Mice, pubmed-meshheading:10878368-Mice, Inbred C3H, pubmed-meshheading:10878368-Mice, Inbred C57BL, pubmed-meshheading:10878368-Mice, Knockout, pubmed-meshheading:10878368-Peritoneal Cavity, pubmed-meshheading:10878368-RNA, Messenger, pubmed-meshheading:10878368-Receptors, Antigen, T-Cell, gamma-delta, pubmed-meshheading:10878368-Receptors, Cell Surface, pubmed-meshheading:10878368-T-Lymphocyte Subsets, pubmed-meshheading:10878368-Toll-Like Receptor 2, pubmed-meshheading:10878368-Toll-Like Receptor 4, pubmed-meshheading:10878368-Toll-Like Receptors
pubmed:year
2000
pubmed:articleTitle
Expression of toll-like receptor 2 on gamma delta T cells bearing invariant V gamma 6/V delta 1 induced by Escherichia coli infection in mice.
pubmed:affiliation
Laboratory of Host Defense and Germfree Life, Research Institute for Disease Mechanism and Control, and First Department of Surgery, Nagoya University School of Medicine, Nagoya, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't