IDO2 is critical for IDO1-mediated T-cell regulation and exerts a non-redundant function in inflammation.
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ABSTRACT: IDO2 is implicated in tryptophan catabolism and immunity but its physiological functions are not well established. Here we report the characterization of mice genetically deficient in IDO2, which develop normally but exhibit defects in IDO-mediated T-cell regulation and inflammatory responses. Construction of this strain was prompted in part by our discovery that IDO2 function is attenuated in macrophages from Ido1 (-/-) mice due to altered message splicing, generating a functional mosaic with implications for interpreting findings in Ido1 (-/-) mice. No apparent defects were observed in Ido2 (-/-) mice in embryonic development or hematopoietic differentiation, with wild-type profiles documented for kynurenine in blood serum and for immune cells in spleen, lymph nodes, peritoneum, thymus a
SUBMITTER: Metz R
PROVIDER: S-EPMC4432394 | biostudies-literature | 2014 Jul
REPOSITORIES: biostudies-literature
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