| Literature DB >> 33264610 |
Marcus J Hines1, Maryaline Coffre1, Tenny Mudianto1, Marisella Panduro2, Eric J Wigton2, Cosmin Tegla1, Victoria Osorio-Vasquez1, Robin Kageyama2, David Benhamou3, Oriana Perez1, Sofia Bajwa1, Michael T McManus4, K Mark Ansel2, Doron Melamed5, Sergei B Koralov6.
Abstract
The phosphatidylinositol 3-kinase (PI3K) signaling cascade downstream of the B cell receptor (BCR) signalosome is essential for B cell maturation. Proper signaling strength is maintained through the PI3K negative regulator phosphatase and tensin homolog (PTEN). Although a role for microRNA (miRNA)-dependent control of the PTEN-PI3K axis has been described, the contribution of individual miRNAs to the regulation of this crucial signaling modality in mature B lymphocytes remains to be elucidated. Our analyses reveal that ablation of miR-29 specifically in B lymphocytes results in an increase in PTEN expression and dampening of the PI3K pathway in mature B cells. This dysregulation has a profound impact on the survival of B lymphocytes and results in increased class switch recombination and decreased plasma cell differentiation. Furthermore, we demonstrate that ablation of one copy of Pten is sufficient to ameliorate the phenotypes associated with miR-29 loss. Our data suggest a critical role for the miR-29-PTEN-PI3K regulatory axis in mature B lymphocytes.Entities:
Keywords: B cell; B lymphocyte; CSR; Class Switch Recombination; PI3K; PTEN; Plasma Cell; Terminal Differentiation; miR-29; miRNA
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Year: 2020 PMID: 33264610 PMCID: PMC7730937 DOI: 10.1016/j.celrep.2020.108436
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423