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BAFF controls B cell metabolic fitness through a PKC beta- and Akt-dependent mechanism.


ABSTRACT: B cell life depends critically on the cytokine B cell-activating factor of the tumor necrosis factor family (BAFF). Lack of BAFF signaling leads to B cell death and immunodeficiency. Excessive BAFF signaling promotes lupus-like autoimmunity. Despite the great importance of BAFF to B cell biology, its signaling mechanism is not well characterized. We show that BAFF initiates signaling and transcriptional programs, which support B cell survival, metabolic fitness, and readiness for antigen-induced proliferation. We further identify a BAFF-specific protein kinase C beta-Akt signaling axis, which provides a connection between BAFF and generic growth factor-induced cellular responses.

SUBMITTER: Patke A 

PROVIDER: S-EPMC2118121 | biostudies-literature | 2006 Oct

REPOSITORIES: biostudies-literature

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BAFF controls B cell metabolic fitness through a PKC beta- and Akt-dependent mechanism.

Patke Alina A   Mecklenbräuker Ingrid I   Erdjument-Bromage Hediye H   Tempst Paul P   Tarakhovsky Alexander A  

The Journal of experimental medicine 20061023 11


B cell life depends critically on the cytokine B cell-activating factor of the tumor necrosis factor family (BAFF). Lack of BAFF signaling leads to B cell death and immunodeficiency. Excessive BAFF signaling promotes lupus-like autoimmunity. Despite the great importance of BAFF to B cell biology, its signaling mechanism is not well characterized. We show that BAFF initiates signaling and transcriptional programs, which support B cell survival, metabolic fitness, and readiness for antigen-induced  ...[more]

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