This proposal seeks to define the intracellular effectors that account for the important role of phosphatidyl inositol-3 kinase (PI3K) signaling in B lymphocyte generation, function and maintenance. Activation of the PI3K signaling network recruits cytosolic effectors to the plasma membrane via pleckstrin homology (PH) domain-binding to PIP3,4,5. In particular, PDK1 has been identified as a pivotal downstream effector of PI3K that activates Akt, p70S6kinase, PKC enzymes and other targets that control cell metabolism, quiescence, proliferation and survival. Recently the Akt kinases have also been shown to negatively regulate the activity of the FOXO transcription factors. In doing so, expression of FOXO target genes is halted, leading to enhance cell cycle progression and survival. In B cells, we posit that the PDK1-dependent pathway acts in synergy with the PIP3,4,5-dependent Btk signaling pathway, which is crucial for NF-kappaB activation and Ca++ mobilization. To address this hypothesis, we will define the relative importance and distinct functions of the PDK1- and Btk-dependent pathways in B cells. Further examination of the PDK1 pathway will be achieved through gene targeting approaches to ablate PDK1, Akt and the FOXO proteins. In addition, we will determine the extent to which Btk, PDK1 and Akt contribute to the splenomegaly/lymphadenopathy and altered B cell differentiation observed in mice lacking Pten in B cells and thus subject to the effects of elevated and sustained PIP3,4,5. Through the generation and characterization of these mice we will learn how PI3K directs B cell differentiation, and provide insight into how such regulation can go awry in the case of B cell transformation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
3R01AI059447-02S1
Application #
7232927
Study Section
Cellular and Molecular Immunology - B (CMI)
Program Officer
Gondre-Lewis, Timothy A
Project Start
2005-06-15
Project End
2010-02-28
Budget Start
2006-06-01
Budget End
2007-02-28
Support Year
2
Fiscal Year
2006
Total Cost
$55,431
Indirect Cost
Name
Sanford-Burnham Medical Research Institute
Department
Type
DUNS #
020520466
City
La Jolla
State
CA
Country
United States
Zip Code
92037
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Baracho, G V; Miletic, A V; Omori, S A et al. (2011) Emergence of the PI3-kinase pathway as a central modulator of normal and aberrant B cell differentiation. Curr Opin Immunol 23:178-83
Browne, Cecille D; Hoefer, Melanie M; Chintalapati, Suresh K et al. (2010) SHEP1 partners with CasL to promote marginal zone B-cell maturation. Proc Natl Acad Sci U S A 107:18944-9
Dengler, Hart S; Baracho, Gisele V; Omori, Sidne A et al. (2008) Distinct functions for the transcription factor Foxo1 at various stages of B cell differentiation. Nat Immunol 9:1388-98
Omori, Sidne A; Rickert, Robert C (2007) Phosphatidylinositol 3-kinase (PI3K) signaling and regulation of the antibody response. Cell Cycle 6:397-402
Omori, Sidne A; Cato, Matthew H; Anzelon-Mills, Amy et al. (2006) Regulation of class-switch recombination and plasma cell differentiation by phosphatidylinositol 3-kinase signaling. Immunity 25:545-57