Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2011-6-27
pubmed:abstractText
Cytotoxic T (Tc) cells play a key role in the defense against virus infections. Tc cells recognize infected cells via the T-cell receptor (TCR) and subsequently kill the target cells by one or more cytotoxic mechanisms. Induction of the cytotoxic mechanisms is finely tuned by the activation signals from the TCR. To determine whether TCR down-regulation affects the cytotoxicity of Tc cells, we studied TCR down-regulation-deficient CD3?LLAA mice. We found that Tc cells from CD3?LLAA mice have reduced cytotoxicity due to a specific deficiency in exocytosis of lytic granules. To determine whether this defect was reflected in an increased susceptibility to virus infections, we studied the course of ectromelia virus (ECTV) infection. We found that the susceptibility to ECTV infection was significantly increased in CD3?LLAA mice with a mortality rate almost as high as in granzyme B knock-out mice. Finally, we found that TCR signaling in CD3?LLAA Tc cells caused highly increased tyrosine phosphorylation and activation of the c-Cbl ubiquitin ligase, and that the impaired exocytosis of lytic granules could be rescued by the knockdown of c-Cbl. Thus, our work demonstrates that TCR down-regulation critically increases Tc cell cytotoxicity and protection against poxvirus infection.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1521-4141
pubmed:author
pubmed:copyrightInfo
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
pubmed:issnType
Electronic
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1948-57
pubmed:meshHeading
pubmed-meshheading:21590764-Animals, pubmed-meshheading:21590764-Antigens, CD3, pubmed-meshheading:21590764-Antigens, CD44, pubmed-meshheading:21590764-Blotting, Western, pubmed-meshheading:21590764-Cell Line, pubmed-meshheading:21590764-Cytotoxicity, Immunologic, pubmed-meshheading:21590764-Ectromelia, Infectious, pubmed-meshheading:21590764-Ectromelia virus, pubmed-meshheading:21590764-Exocytosis, pubmed-meshheading:21590764-Granzymes, pubmed-meshheading:21590764-Mice, pubmed-meshheading:21590764-Mice, Inbred C57BL, pubmed-meshheading:21590764-Mice, Knockout, pubmed-meshheading:21590764-Mice, Transgenic, pubmed-meshheading:21590764-Perforin, pubmed-meshheading:21590764-Phosphorylation, pubmed-meshheading:21590764-Proto-Oncogene Proteins c-cbl, pubmed-meshheading:21590764-RNA, Small Interfering, pubmed-meshheading:21590764-RNA Interference, pubmed-meshheading:21590764-Receptors, Antigen, T-Cell, pubmed-meshheading:21590764-T-Lymphocytes, Cytotoxic, pubmed-meshheading:21590764-Ubiquitin-Protein Ligases
pubmed:year
2011
pubmed:articleTitle
TCR down-regulation boosts T-cell-mediated cytotoxicity and protection against poxvirus infections.
pubmed:affiliation
Department of International Health, Immunology and Microbiology, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't