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Induction of GTP‐cyclohydrolase I mRNA expression by lectin activation and interferon‐γ treatment in human cells associated with the immune response
Author(s) -
Schott Karin,
Gütlich Markus,
Ziegler Irmgard
Publication year - 1993
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041560103
Subject(s) - gtp cyclohydrolase i , tetrahydrobiopterin , gtp' , biopterin , messenger rna , interferon , immune system , cytokine , microbiology and biotechnology , chemistry , biology , enzyme , biochemistry , cofactor , immunology , gene
The development of tetrahydrobiopterin synthesis during lectin stimulation of resting human T lymphocytes (Kerler et al. [1989] FEBS Lett., 250 :622–624), the interferon‐γ induced neopterin production by human monocytes/macrophages (Huber et al. [1984] J. Exp. Med., 160 :310–16), and the control of tetrahydrobiopterin synthesis in activated T cells by the synergistic action of interferon‐γ and interleukin 2 (Ziegler et al. [1990] J. Biol. Chem., 265 :17026–17030) were previously explained by modulation of the apparent GTP‐cyclohydrolase I activation. In this study we demonstrate that increases in GTP‐cyclohydrolase I activity which occur after lectin induction and after cytokine treatment correlate with increased steady state mRNA levels specific for this enzyme. The enhancement of interferon‐γ induced enzyme activity in primed T cells by interleukin 2 also corresponds to further increases in mRNA expression. The steady state GTP‐cyclohydrolase I mRNA levels in primed T cells, however, do not correlate with the steep decline which follows the culmination of enzyme activity 44 hours after treatment. This indicates that the down‐regulation of apparent GTP‐cyclohydrolase I activity is caused by posttranslational modification of the protein. © 1993 Wiley‐Liss, Inc.