| Literature DB >> 23623381 |
Jorge Henao-Mejia1, Adam Williams, Loyal A Goff, Matthew Staron, Paula Licona-Limón, Susan M Kaech, Maki Nakayama, John L Rinn, Richard A Flavell.
Abstract
Regulation of metabolic pathways in the immune system provides a mechanism to actively control cellular function, growth, proliferation, and survival. Here, we report that miR-181 is a nonredundant determinant of cellular metabolism and is essential for supporting the biosynthetic demands of early NKT cell development. As a result, miR-181-deficient mice showed a complete absence of mature NKT cells in the thymus and periphery. Mechanistically, miR-181 modulated expression of the phosphatase PTEN to control PI3K signaling, which was a primary stimulus for anabolic metabolism in immune cells. Thus miR-181-deficient mice also showed severe defects in lymphoid development and T cell homeostasis associated with impaired PI3K signaling. These results uncover miR-181 as essential for NKT cell development and establish this family of miRNAs as central regulators of PI3K signaling and global metabolic fitness during development and homeostasis.Entities:
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Year: 2013 PMID: 23623381 PMCID: PMC3738211 DOI: 10.1016/j.immuni.2013.02.021
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745