Abstract
Apoptosis-inducing factor (Aif) is a mitochondrial flavoprotein that regulates cell metabolism and survival in many tissues. We report that aif-hypomorphic harlequin (Hq) mice show thymic hypocellularity and a cell-autonomous thymocyte developmental block associated with apoptosis at the β-selection stage, independent of T cell receptor β recombina-tion. No abnormalities are observed in the B cell lineage. Transgenes encoding wild-type or DNA-binding-deficient mutant Aif rectify the thymic defect, but a transgene encoding oxidoreductase activity-deficient mutant Aif does not. The Hq thymic block is reversed in vivo by antioxidant treatment, and Hq T but not B lineage cells show enhanced oxidative stress. Thus, Aif, a ubiquitous protein, serves a lineage-specific nonredundant antiapoptotic role in the T cell lineage by regulating reactive oxygen species during thymic β-selection. © 2012 Banerjee et al.
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CITATION STYLE
Banerjee, H., Das, A., Srivastava, S., Mattoo, H. R., Thyagarajan, K., Khalsa, J. K., … Rath, S. (2012). A role for apoptosis-inducing factor in T cell development. Journal of Experimental Medicine, 209(9), 1641–1653. https://doi.org/10.1084/jem.20110306
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