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Control of pteridine biosynthesis in the natural killer-like cell line YT.

作者信息

Schott K, Yodoi J, Schwuléra U, Ziegler I

机构信息

GSF-Forschungszentrum für Umwelt und Gesundheit, GmbH, Institut für Experimentelle Hämatologie, München, FRG.

出版信息

Biochem Biophys Res Commun. 1991 May 15;176(3):1430-6. doi: 10.1016/0006-291x(91)90446-e.

DOI:10.1016/0006-291x(91)90446-e
PMID:2039522
Abstract

The natural killer-like cell line YT constitutively expresses GTP-cyclohydrolase activity whereas 6-pyruvoyltetrahydropterin synthase and sepiapterin reductase are absent. The product, dihydroneopterin triphosphate, is dephosphorylated and oxidized causing neopterin to accumulate in the cells. The activities of the H4biopterin synthesizing enzymes are not controlled by IFN-gamma or the synergistic action of both IFN-gamma and IL-2 as has been shown for monocytes/macrophages (Huber C. et al. (1984) J. Exp. Med. 160, 310) and CD4+ T cells, respectively (Ziegler I. et al. (1990) J. Biol. Chem. 265, 17026). Sepiapterin reductase specifically is induced by incubation of the cells with sepiapterin, leaving GTP-cyclohydrolase, 6-pyruvoyltetrahydropterin synthase and other enzymes related to pteridine metabolism (dihydropteridine reductase, dihydrofolate reductase) unaffected. The data indicate that H4biopterin synthesis is individually regulated in the diverse cellular components of the immune system.

摘要

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