Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1997-3-5
|
pubmed:abstractText |
Lymphocytes circulating in the bloodstream home into lymph nodes (LN). T cells predominate in peripheral LN (PLN) and B cells in spleen or mucosal tissue, e.g. Peyer's patches (PP). DDD/1 mice are unique in marked paucity of LN cells, especially T cells. T cell frequency in PLN was 20-40% in this strain, compared to 60-80% in others. Immunohistochemistry confirmed the low density of T cells in the subcortical area but normal colonization of B cells in cortical area in PLN of DDD/1. In contrast, the T cell content of peripheral blood and spleen was higher in DDD/1 but that in PP was not significantly different compared to other strains. It was thus concluded that this abnormality in DDD/1 results from a homing defect of T cells into PLN but not from lymphopenia. Genetical analysis showed that the defect in T cell-specific homing was regulated by a single autosomal recessive gene, tentatively designated plt (paucity of lymph node T cells). Reciprocal bone marrow transplantation indicated that the plt phenotype may arise from some defect in PLN stroma but not in lymphocytes. An in vivo homing assay using fluorescence-labeled lymphocytes demonstrated that the homing defect was specific for T cells but not for B cells. A Stamper-Woodruff assay revealed that the binding between lymphocytes and PLN high endothelial venules was normal and that L-selectin and its ligand, peripheral node vascular addressin (PNAd), were expressed and functioned normally in DDD/1. These results taken together indicate that the T cell-specific homing into PLN is disturbed at a post-adhesion stage in DDD/1. The product of the plt locus may play a pivotal role at this stage.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD45,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Surface,
http://linkedlifedata.com/resource/pubmed/chemical/L-Selectin,
http://linkedlifedata.com/resource/pubmed/chemical/L-selectin counter-receptors,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0014-2980
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
27
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
215-21
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9022021-Animals,
pubmed-meshheading:9022021-Antigens, CD45,
pubmed-meshheading:9022021-Antigens, Surface,
pubmed-meshheading:9022021-Cell Movement,
pubmed-meshheading:9022021-Chemotaxis, Leukocyte,
pubmed-meshheading:9022021-Female,
pubmed-meshheading:9022021-L-Selectin,
pubmed-meshheading:9022021-Lymph Nodes,
pubmed-meshheading:9022021-Membrane Proteins,
pubmed-meshheading:9022021-Mice,
pubmed-meshheading:9022021-Mice, Inbred BALB C,
pubmed-meshheading:9022021-Mice, Inbred C3H,
pubmed-meshheading:9022021-Mice, Inbred C57BL,
pubmed-meshheading:9022021-Mice, Mutant Strains,
pubmed-meshheading:9022021-Peyer's Patches,
pubmed-meshheading:9022021-T-Lymphocytes
|
pubmed:year |
1997
|
pubmed:articleTitle |
Genetic defect in T lymphocyte-specific homing into peripheral lymph nodes.
|
pubmed:affiliation |
Laboratory Animal Research Center, University of Tokyo, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|