pubmed-article:11104809 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11104809 | lifeskim:mentions | umls-concept:C0115305 | lld:lifeskim |
pubmed-article:11104809 | lifeskim:mentions | umls-concept:C0024264 | lld:lifeskim |
pubmed-article:11104809 | lifeskim:mentions | umls-concept:C1419941 | lld:lifeskim |
pubmed-article:11104809 | lifeskim:mentions | umls-concept:C0023688 | lld:lifeskim |
pubmed-article:11104809 | lifeskim:mentions | umls-concept:C0205463 | lld:lifeskim |
pubmed-article:11104809 | lifeskim:mentions | umls-concept:C0600210 | lld:lifeskim |
pubmed-article:11104809 | lifeskim:mentions | umls-concept:C0086597 | lld:lifeskim |
pubmed-article:11104809 | pubmed:issue | 11 | lld:pubmed |
pubmed-article:11104809 | pubmed:dateCreated | 2000-12-26 | lld:pubmed |
pubmed-article:11104809 | pubmed:abstractText | P-selectin glycoprotein ligand 1 (PSGL-1) is a sialomucin expressed on leukocytes that mediates neutrophil rolling on the vascular endothelium. Here, the role of PSGL-1 in mediating lymphocyte migration was studied using mice lacking PSGL-1. In a contact hypersensitivity model, the infiltration of CD4(+) T lymphocytes into the inflamed skin was reduced in PSGL-1-deficient mice. In vitro-generated T helper (Th)1 cells from PSGL-1-deficient mice did not bind to P-selectin and migrated less efficiently into the inflamed skin than wild-type Th1 cells. To assess the role of PSGL-1 in P- or E-selectin-mediated migration of Th1 cells, the cells were injected into E- or P-selectin-deficient mice. PSGL-1-deficient Th1 cells did not migrate into the inflamed skin of E-selectin-deficient mice, indicating that PSGL-1 on Th1 cells is the sole ligand for P-selectin in vivo. In contrast, PSGL-1-deficient Th1 cells migrated into the inflamed skin of P-selectin-deficient mice, although less efficiently than wild-type Th1 cells. This E-selectin-mediated migration of PSGL-1-deficient or wild-type Th1 cells was not altered by injecting a blocking antibody to L-selectin. These data provide evidence that PSGL-1 on Th1 cells functions as one of the E-selectin ligands in vivo. | lld:pubmed |
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pubmed-article:11104809 | pubmed:language | eng | lld:pubmed |
pubmed-article:11104809 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11104809 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11104809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11104809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:11104809 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11104809 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11104809 | pubmed:month | Dec | lld:pubmed |
pubmed-article:11104809 | pubmed:issn | 0022-1007 | lld:pubmed |
pubmed-article:11104809 | pubmed:author | pubmed-author:FurieBB | lld:pubmed |
pubmed-article:11104809 | pubmed:author | pubmed-author:FurieB CBC | lld:pubmed |
pubmed-article:11104809 | pubmed:author | pubmed-author:HirataTT | lld:pubmed |
pubmed-article:11104809 | pubmed:author | pubmed-author:YangJJ | lld:pubmed |
pubmed-article:11104809 | pubmed:author | pubmed-author:BER | lld:pubmed |
pubmed-article:11104809 | pubmed:author | pubmed-author:Merrill-Skolo... | lld:pubmed |
pubmed-article:11104809 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11104809 | pubmed:day | 4 | lld:pubmed |
pubmed-article:11104809 | pubmed:volume | 192 | lld:pubmed |
pubmed-article:11104809 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11104809 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11104809 | pubmed:pagination | 1669-76 | lld:pubmed |
pubmed-article:11104809 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:11104809 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:11104809 | pubmed:articleTitle | P-Selectin glycoprotein ligand 1 (PSGL-1) is a physiological ligand for E-selectin in mediating T helper 1 lymphocyte migration. | lld:pubmed |
pubmed-article:11104809 | pubmed:affiliation | Center for Hemostasis and Thrombosis Research, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215, USA. | lld:pubmed |
pubmed-article:11104809 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11104809 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
entrez-gene:20345 | entrezgene:pubmed | pubmed-article:11104809 | lld:entrezgene |
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