rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
12
|
pubmed:dateCreated |
2003-11-25
|
pubmed:abstractText |
T cells encounter two main checkpoints during development in the thymus. These checkpoints are critically dependent on signals derived from the thymic microenvironment as well as from the pre-T cell receptor (pre-TCR) and the alphabeta TCR. Here we show that T cell-specific deletion of beta-catenin impaired T cell development at the beta-selection checkpoint, leading to a substantial decrease in splenic T cells. In addition, beta-catenin also seemed to be a target of TCR-CD3 signals in thymocytes and mature T cells. These data indicate that beta-catenin-mediated signals are required for normal T cell development.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
1529-2908
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
4
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1177-82
|
pubmed:dateRevised |
2007-11-8
|
pubmed:meshHeading |
pubmed-meshheading:14608382-Animals,
pubmed-meshheading:14608382-Cell Differentiation,
pubmed-meshheading:14608382-Cytoskeletal Proteins,
pubmed-meshheading:14608382-Flow Cytometry,
pubmed-meshheading:14608382-Gene Deletion,
pubmed-meshheading:14608382-Immune System,
pubmed-meshheading:14608382-Immunity, Cellular,
pubmed-meshheading:14608382-Mice,
pubmed-meshheading:14608382-Mice, Transgenic,
pubmed-meshheading:14608382-Polymerase Chain Reaction,
pubmed-meshheading:14608382-Receptors, Antigen, T-Cell,
pubmed-meshheading:14608382-Spleen,
pubmed-meshheading:14608382-T-Lymphocytes,
pubmed-meshheading:14608382-Trans-Activators,
pubmed-meshheading:14608382-beta Catenin
|
pubmed:year |
2003
|
pubmed:articleTitle |
Deletion of beta-catenin impairs T cell development.
|
pubmed:affiliation |
Dana Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|