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J Immunol. 2001 Feb 15;166(4):2173-7.

Cutting edge: Stat6-dependent substrate depletion regulates nitric oxide production.

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1
Department of Infectious Diseases, Howard Hughes Medical Institute, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Erratum in

  • J Immunol 2001 Apr 1;166(7):4788.

Abstract

The cytokines IL-4 and IL-13 inhibit the production of NO from activated macrophages through an unresolved molecular mechanism. We show here that IL-4 and IL-13 regulate NO production through depletion of arginine, the substrate of inducible NO synthase (iNOS). Inhibition of NO production from murine macrophages stimulated with LPS and IFN-gamma by IL-4 or IL-13 was dependent on Stat6, cell density in the cultures, and pretreatment for at least 6 h. IL-4/IL-13 did not interfere with the expression or activity of iNOS but up-regulated arginase I (the liver isoform of arginase) in a Stat6-dependent manner. Addition of exogenous arginine completely restored NO production in IL-4-treated macrophages. Furthermore, impaired killing of the intracellular pathogen Toxoplasma gondii in IL-4-treated macrophages was overcome by supplementing L-arginine. The simple system of regulated substrate competition between arginase and iNOS has implications for understanding the physiological regulation of NO production.

PMID:
11160269
DOI:
10.4049/jimmunol.166.4.2173
[Indexed for MEDLINE]
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