| Literature DB >> 27880903 |
Maryaline Coffre1, David Benhamou2, David Rieß3, Lili Blumenberg1, Valentina Snetkova1, Marcus J Hines1, Tirtha Chakraborty3, Sofia Bajwa1, Kari Jensen3, Mark M W Chong4, Lelise Getu5, Gregg J Silverman6, Robert Blelloch7, Dan R Littman8, Dinis Calado3, Doron Melamed2, Jane A Skok1, Klaus Rajewsky3, Sergei B Koralov9.
Abstract
B cell development is a tightly regulated process dependent on sequential rearrangements of immunoglobulin loci that encode the antigen receptor. To elucidate the role of microRNAs (miRNAs) in the orchestration of B cell development, we ablated all miRNAs at the earliest stage of B cell development by conditionally targeting the enzymes critical for RNAi in early B cell precursors. Absence of any one of these enzymes led to a block at the pro- to pre-B cell transition due to increased apoptosis and a failure of pre-B cells to proliferate. Expression of a Bcl2 transgene allowed for partial rescue of B cell development, however, the majority of the rescued B cells had low surface immunoglobulin expression with evidence of ongoing light chain editing. Our analysis revealed that miRNAs are critical for the regulation of the PTEN-AKT-FOXO1 pathway that in turn controls Rag expression during B cell development. Copyright ÂEntities:
Keywords: B cell development; B lymphocytes; DGCR8; Dicer; Drosha; PI3K/AKT; PTEN; RAG; miRNA; receptor editing
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Year: 2016 PMID: 27880903 PMCID: PMC5679080 DOI: 10.1016/j.celrep.2016.11.006
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423