Upregulation of intercellular adhesion molecule-1 expression on human endothelial cells by tumour necrosis factor-α in an in vitro model of the blood-brain
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Dobbie, MS
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机构:Univ W England, Fac Sci Appl, Dept Biol & Biomed Sci, Bristol BS16 1QY, Avon, England
Dobbie, MS
Hurst, RD
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机构:Univ W England, Fac Sci Appl, Dept Biol & Biomed Sci, Bristol BS16 1QY, Avon, England
Hurst, RD
Klein, NJ
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机构:Univ W England, Fac Sci Appl, Dept Biol & Biomed Sci, Bristol BS16 1QY, Avon, England
Klein, NJ
Surtees, RAH
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机构:Univ W England, Fac Sci Appl, Dept Biol & Biomed Sci, Bristol BS16 1QY, Avon, England
Surtees, RAH
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[1] Univ W England, Fac Sci Appl, Dept Biol & Biomed Sci, Bristol BS16 1QY, Avon, England
[2] Univ London, Inst Child Hlth, London WC1N 1EH, England
Adhesion molecules on the endothelial surface of the blood-brain barrier (BBB) play an important role in the pathogenesis of many encephalopathies, including multiple sclerosis (MS) and cerebral malaria; (CM). The expression of four surface molecules of relevance to MS and CM on the immortalized human umbilical vein endothelial cell line, ECV304, was investigated using immunofluorescence flow cytometry. We found that ECV304 cells express intercellular adhesion molecule-1 (ICAM-1) and low levels of CD36, but not vascular cell adhesion molecule-1 (VCAM-1) or E-selectin. This expression pattern was unaltered on ECV304 cells which were co-cultured with C6 glioma cells; conditions under which the endothelial cells display enhanced barrier formation. Tumour necrosis factor-alpha (TNF-alpha), which is elevated in MS and CM, decreased the integrity of the barrier in co-cultured endothelial cells and upregulated the expression of ICAM-1 nine-fold. The significance of elevated ICAM-1 expression in relation to the binding of parasitised erythrocytes at the BBB in CM is discussed. (C) 1999 Elsevier Science B.V. All rights reserved.
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UNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLANDUNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLAND
ADAMS, CWM
POSTON, RN
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UNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLANDUNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLAND
POSTON, RN
BUK, SJ
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UNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLANDUNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLAND
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UNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLANDUNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLAND
ADAMS, CWM
POSTON, RN
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UNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLANDUNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLAND
POSTON, RN
BUK, SJ
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UNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLANDUNIV LONDON,UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV HISTOPATHOL,LONDON,ENGLAND