Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1996-7-17
pubmed:abstractText
The migration of lymphocytes through monolayers of rat retinal pigment epithelium (RPE) and retinal vascular endothelium, which form the posterior and anterior blood-retinal barrier (BRB) respectively, was investigated in vitro. After a 4-hr assay the migration of untreated peripheral lymph node (PLN) cells through RPE monolayers was negligible (<1%) with only a small increase found after activation of the PLN cells with concanavalin A or by cross-linking CD3. Activation of the RPE with IFN-gamma augmented migration with maximal PLN cell migration being achieved with a combination of CD3 cross-linking and IFN-gamma activation (17% migration). The highest level of lymphocyte migration was observed with three CD4+ antigen-specific T cell lines specific for purified protein derivative (PPD; 33% migration), ovalbumin (OA; 31%), and S-antigen (S-Ag; 57%). Migration of both untreated and Con A-activated PLN cells through retinal endothelial cells (EC) from PVG rats was negligible, whereas the migration of the antigen-specific T cell lines was 23, 29 and 23% for PPD, OA, and S-Ag lines, respectively. Migration of these cell lines through retinal endothelium derived from Lewis rats was significantly greater (44% for PPD, 39% for OA, and 39% for S-Ag) which corresponded with a greater expression of ICAM-1 on the EC.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0008-8749
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
168
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
267-75
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:8640874-Animals, pubmed-meshheading:8640874-Antigens, pubmed-meshheading:8640874-Arrestin, pubmed-meshheading:8640874-Blood-Retinal Barrier, pubmed-meshheading:8640874-Cell Adhesion, pubmed-meshheading:8640874-Cell Line, pubmed-meshheading:8640874-Chemotaxis, Leukocyte, pubmed-meshheading:8640874-Endothelium, Vascular, pubmed-meshheading:8640874-Eye Proteins, pubmed-meshheading:8640874-Interferon-gamma, pubmed-meshheading:8640874-Interleukin-1, pubmed-meshheading:8640874-Lymph Nodes, pubmed-meshheading:8640874-Lymphocyte Activation, pubmed-meshheading:8640874-Lymphocyte Subsets, pubmed-meshheading:8640874-Muromonab-CD3, pubmed-meshheading:8640874-Ovalbumin, pubmed-meshheading:8640874-Pigment Epithelium of Eye, pubmed-meshheading:8640874-Rats, pubmed-meshheading:8640874-Rats, Inbred Lew, pubmed-meshheading:8640874-Rats, Inbred Strains, pubmed-meshheading:8640874-Receptor-CD3 Complex, Antigen, T-Cell, pubmed-meshheading:8640874-Recombinant Proteins, pubmed-meshheading:8640874-Retinal Vessels, pubmed-meshheading:8640874-Specific Pathogen-Free Organisms, pubmed-meshheading:8640874-T-Lymphocytes, Helper-Inducer, pubmed-meshheading:8640874-Tuberculin
pubmed:year
1996
pubmed:articleTitle
Lymphocyte migration across the anterior and posterior blood-retinal barrier in vitro.
pubmed:affiliation
Department of Clinical Science, Institute of Ophthalmology, University College London, United Kingdom.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't