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Direct observations of the kinetics of migrating T-cells suggest active retention by endothelial cells with continual bidirectional migration.

McGettrick, Helen M. and Hunter, Kirsty and Moss, Paul A. and Buckley, Christopher D. and Rainger, G. Ed and Nash, Gerard B. (2008) Direct observations of the kinetics of migrating T-cells suggest active retention by endothelial cells with continual bidirectional migration. Journal of Leukocyte Biology. ISSN 0741-5400 (Submitted)

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Identification Number/DOI: 10.1189/jlb.0508301

The kinetics and regulatory mechanisms of T-cell migration through endothelium have not been fully defined. In experimental filter-based assays in vitro, transmigration of lymphocytes takes hours, compared to minutes in vivo. We cultured endothelial cell (EC) monolayers on filters, solid substrates or collagen gels, and treated them with tumour necrosis factor-α (TNF), interferon-γ (IFN), or both, prior to analysis of lymphocyte migration in the presence or absence of flow. Peripheral blood lymphocytes (PBL), CD4+ cells or CD8+ cells, took many hours to migrate through EC-filter constructs for all cytokine treatments. However, direct microscopic observations of EC-filters which had been mounted in a flow chamber showed that PBL crossed the endothelial monolayer in minutes and were highly motile in the subendothelial space. Migration through EC was also observed on clear plastic, with or without flow. After brief settling without flow, PBL and isolated CD3+ or CD4+ cells all crossed EC in minutes, but the numbers of migrated cells varied little with time. Close observation revealed that lymphocytes continuously migrated back and forth across endothelium. Under flow, migration kinetics and the proportions migrating back and forth were little altered. On collagen gels, PBL again crossed EC in minutes and migrated back and forth, but showed little penetration of the gel over hours.In contrast, neutrophils migrated efficiently through EC and into gels. These observations suggest a novel model for lymphoid migration, in which endothelial cells support migration but retain lymphocytes (as opposed to neutrophils), and additional signal(s) are required for onward migration.

Type of Work:Article
Date:19 September 2008 (Submission)
School/Faculty:Colleges (2008 onwards) > College of Medical & Dental Sciences
Department:Division of Medical Studies, Division of Cancer Studies, Division of Immunity and Infection
Subjects:R Medicine (General)
Institution:University of Birmingham
Copyright Holders:Oxford journals
ID Code:100
Refereed:YES
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