| Literature DB >> 18703361 |
Adam K Savage1, Michael G Constantinides, Jin Han, Damien Picard, Emmanuel Martin, Bofeng Li, Olivier Lantz, Albert Bendelac.
Abstract
The transcriptional control of CD1d-restricted NKT cell development has remained elusive. We report that PLZF (promyelocytic leukemia zinc finger, Zbtb16), a member of the BTB/POZ-ZF family of transcription factors that includes the CD4-lineage-specific c-Krox (Th-POK), is exquisitely specific to CD1d-restricted NKT cells and human MR1-specific MAIT cells. PLZF was induced immediately after positive selection of NKT cell precursors, and PLZF-deficient NKT cells failed to undergo the intrathymic expansion and effector differentiation that characterize their lineage. Instead, they preserved a naive phenotype and were directed to lymph nodes. Conversely, transgenic expression of PLZF induced CD4(+) thymocytes to acquire effector differentiation and migrate to nonlymphoid tissues. We suggest that PLZF is a transcriptional signature of NKT cells that directs their innate-like effector differentiation during thymic development.Entities:
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Year: 2008 PMID: 18703361 PMCID: PMC2613001 DOI: 10.1016/j.immuni.2008.07.011
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745