4.8 Article

PI3 Kinase Signals BCR-Dependent Mature B Cell Survival

Journal

CELL
Volume 139, Issue 3, Pages 573-586

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2009.08.041

Keywords

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Funding

  1. NIH [AI054636, CA092625, AI014782-31]
  2. Leukemia and Lymphoma Society
  3. European Union through MUGEN
  4. Hematology and Transfusion Medicine at Harvard Medical School
  5. Portuguese Foundation for Science and Technology
  6. Robert A. and Renee E. Belfer Foundation

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Previous work has shown that mature B cells depend upon survival signals delivered to the cells by their antigen receptor (BCR). To identify the molecular nature of this survival signal, we have developed a genetic approach in which ablation of the BCR is combined with the activation of specific, BCR dependent signaling cascades in mature B cells in vivo. Using this system, we provide evidence that the survival of BCR deficient mature B cells can be rescued by a single signaling pathway downstream of the BCR, namely PI3K signaling, with the FOXO1 transcription factor playing a central role.

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