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Selective inhibition of human glial inducible nitric oxide synthase by interferon-beta: implications for multiple sclerosis.

作者信息

Hua L L, Liu J S, Brosnan C F, Lee S C

机构信息

Department of Pathology (Neuropathology), Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Ann Neurol. 1998 Mar;43(3):384-7. doi: 10.1002/ana.410430317.

DOI:10.1002/ana.410430317
PMID:9506556
Abstract

Nitric oxide generated from the inducible nitric oxide synthase (iNOS) has been implicated in the pathogenesis of multiple sclerosis. Because significant species- and cell-specific differences exist in the expression of iNOS, we used primary human glial cell cultures to screen for an inhibitor of iNOS expression. Remarkably, among numerous soluble factors tested, interferon-beta (IFN-beta) alone showed a selective and potent inhibition of interleukin-1beta/interferon-gamma (IL-1beta/IFN-gamma)-induced iNOS expression in astrocytes. Inhibition of iNOS may provide a mechanism by which IFN-beta can ameliorate inflammation and cytotoxicity in the central nervous system of patients with multiple sclerosis.

摘要

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