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American Journal of Pathology, Vol 143, 337-341, Copyright © 1993 by American Society for Investigative Pathology
REGULAR ARTICLES |
ML Estes, K Iwasaki, BS Jacobs and BP Barna
Division of Pathology and Laboratory Medicine, Cleveland Clinic, Ohio 44195.
The T lymphocyte-derived cytokine, interleukin-4 (IL-4), was found to inhibit dose dependently basal DNA synthesis of cultured non-neoplastic human astrocytes isolated from epilepsy white matter tissue. The mitogenic effect of tumor necrosis factor on astrocytes was also inhibited by IL-4, and the inhibitory effect was abrogated by anti-IL-4 antibody but not by irrelevant IgG. Immunofluorescent analysis indicated significantly reduced numbers of glial fibrillary acidic protein-positive astrocytes incorporating nuclear bromodeoxyuridine in IL-4-treated cultures compared to control. These findings indicate that human adult astrocyte proliferation, in contrast to that reported for endothelial cells or fibroblasts, is sensitive to down-regulation by IL- 4.
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