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Transforming growth factor–beta inhibition of cytokine-induced vascular cell adhesion molecule-1 expression in human astrocytes

✍ Scribed by Margaret K. Winkler; Etty N. Benveniste


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
156 KB
Volume
22
Category
Article
ISSN
0894-1491

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✦ Synopsis


Leukocyte transmigration across the blood-brain barrier (BBB) is a cardinal feature of central nervous system (CNS) inflammation. Astrocytes form an integral part, both structurally and functionally, of the BBB. Vascular cell adhesion molecule-1 (VCAM-1), a member of the immunoglobulin gene superfamily, is involved in extravasation into inflamed tissues and activation of T-lymphocytes. In this study, we investigated the role of TGF-␤, an immunosuppressive cytokine, in regulating cytokineinduced VCAM-1 expression in astrocytes. Human astroglioma cell lines and primary human fetal astrocytes were examined for VCAM-1 gene expression after treatment with proinflammatory cytokines (TNF-␣, IL-1␤, IFN-␥) in the absence or presence of TGF-␤. Astroglioma cell lines as well as primary human fetal astrocytes expressed low levels of VCAM-1 constitutively, and the proinflammatory cytokines induced marked increases in VCAM-1 expression, particularly TNF-␣ and IL-1␤. The inclusion of TGF-␤1 or TGF-␤2 with the proinflammatory cytokines inhibited VCAM-1 gene expression to varying degrees (33-93%) in all the astroglioma cell lines and primary fetal cells. These results indicate that TGF-␤ is an important regulator of cytokine induced VCAM-1 expression on astrocytes and may prove useful clinically in controlling CNS inflammation.


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