pubmed-article:7836740 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0225336 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0934502 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0003320 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0221912 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0079717 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0209606 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C1704675 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0600210 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C1314939 | lld:lifeskim |
pubmed-article:7836740 | lifeskim:mentions | umls-concept:C0050156 | lld:lifeskim |
pubmed-article:7836740 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:7836740 | pubmed:dateCreated | 1995-2-27 | lld:pubmed |
pubmed-article:7836740 | pubmed:abstractText | The cutaneous lymphocyte-associated Ag (CLA) is expressed by a subset of circulating memory/effector T cells and by the vast majority of skin-infiltrating T cells. CLA is thought to target skin-associated T cells to inflammatory skin sites by interacting with endothelial cell ligand E-selectin (CD62E). We have examined adhesion molecules involved in the migration of human CLA+ and CLA- memory/effector T lymphocytes through IL-1- and TNF-alpha-activated and nonactivated HUVEC layers under static (nonflow) conditions. CLA-enriched memory/effector T lymphocytes migrated more actively across cytokine-activated HUVEC than CLA-depleted memory/effector T cells. This enhanced migration is dependent on the CLA/E-selectin interaction. mAb to very late Ag-4 (VLA-4) and vascular cell adhesion molecule-1 (VCAM-1) blocked the migration of CLA-enriched, but not of CLA-depleted, T cells across activated HUVEC. The observation that anti-VLA-4 and anti-CLA mAb did not show additional inhibition supports the concept that CLA and VLA-4 are sequentially involved in the extravasation. The fact that only CLA+ T cells were inhibited by the anti-VLA-4 mAb suggests that, in this system, CLA engagement is required for using the VLA-4/VCAM-1 pathway. Our studies demonstrate that CLA+ T cells use LFA-1/intercellular leukocyte adhesion molecule-1 (ICAM-1) for transmigration but that CLA expression is not required for the LFA-1/ICAM-1-dependent transmigration because anti-CD18/CD11a mAbs and anti-ICAM-1 mAbs were able to block T cell migration regardless of the activation state of HUVEC or the CLA expression by T cells. Taken together, our results suggest that CLA has a homing function in conducting the T cell to interact with LFA-1/ICAM-1 and/or VLA-4/VCAM-1; this results in enhanced adhesion and migration across cytokine-activated endothelial cells. | lld:pubmed |
pubmed-article:7836740 | pubmed:language | eng | lld:pubmed |
pubmed-article:7836740 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7836740 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:7836740 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:7836740 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:7836740 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7836740 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7836740 | pubmed:month | Feb | lld:pubmed |
pubmed-article:7836740 | pubmed:issn | 0022-1767 | lld:pubmed |
pubmed-article:7836740 | pubmed:author | pubmed-author:BlaserKK | lld:pubmed |
pubmed-article:7836740 | pubmed:author | pubmed-author:MosesSS | lld:pubmed |
pubmed-article:7836740 | pubmed:author | pubmed-author:HausenGG | lld:pubmed |
pubmed-article:7836740 | pubmed:author | pubmed-author:PickerL JLJ | lld:pubmed |
pubmed-article:7836740 | pubmed:author | pubmed-author:Santamaria... | lld:pubmed |
pubmed-article:7836740 | pubmed:author | pubmed-author:Perez... | lld:pubmed |
pubmed-article:7836740 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7836740 | pubmed:day | 15 | lld:pubmed |
pubmed-article:7836740 | pubmed:volume | 154 | lld:pubmed |
pubmed-article:7836740 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7836740 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7836740 | pubmed:pagination | 1543-50 | lld:pubmed |
pubmed-article:7836740 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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pubmed-article:7836740 | pubmed:meshHeading | pubmed-meshheading:7836740-... | lld:pubmed |
pubmed-article:7836740 | pubmed:year | 1995 | lld:pubmed |
pubmed-article:7836740 | pubmed:articleTitle | Migration of skin-homing T cells across cytokine-activated human endothelial cell layers involves interaction of the cutaneous lymphocyte-associated antigen (CLA), the very late antigen-4 (VLA-4), and the lymphocyte function-associated antigen-1 (LFA-1). | lld:pubmed |
pubmed-article:7836740 | pubmed:affiliation | Swiss Institute of Allergy and Asthma Research, Davos. | lld:pubmed |
pubmed-article:7836740 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7836740 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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