The actin cytoskeleton is a dynamic cellular network known for its function in cell morphology and motility. Recent studies using high resolution and real time imaging techniques have revealed that actin plays a critical role in signal transduction, primarily by modulating the dynamics and organization of membrane-associated receptors and signaling molecules. This review summarizes what we have learned so far about a regulatory niche of the actin cytoskeleton in the signal transduction of the B cell receptor (BCR). The activation of the BCR is initiated and regulated by a close coordination between the dynamics of surface BCRs and the cortical actin network. The actin cytoskeleton is involved in regulating the signaling threshold of the BCR to antigenic stimulation, the kinetics and amplification of BCR signaling activities, and the timing and kinetics of signaling downregulation. Actin exerts its regulatory function by controlling the kinetics, magnitude, subcellular location, and nature of BCR clustering and BCR signaling complex formation at every stage of signaling. The cortical actin network is remodeled by initial detachment from the plasma membrane, disassembly and subsequent reassembly into new actin structures in response to antigenic stimulation. Signaling responsive actin regulators translate BCR stimulatory and inhibitory signals into a series of actin remodeling events, which enhance signaling activation and down-regulation by modulating the lateral mobility and spatial organization of surface BCR. The mechanistic understanding of actin-mediated signaling regulation in B cells will help us explore B cell-specific manipulations of the actin cytoskeleton as treatments for B cell-mediated autoimmunity and B cell cancer. This article is part of a Special Issue entitled: Reciprocal influences between cell cytoskeleton and membrane channels, receptors and transporters. Guest Editor: Jean Claude Hervé.
Keywords: Abp1; Actin regulator; B cell; B cell receptor; BCR; Bruton's tyrosine kinase; Btk; ERM; ITAMs; N-WASP; PI(3,4,5)P(3); PI3K; PLCγ2; SSH; Signal transduction; TLR; The actin cytoskeleton; Toll-like receptor; WASP; Wiskott–Aldrich syndrome protein; actin binding protein 1; ezrin/radixin/moesin; immunoreceptor tyrosine-based activation motifs; mIg; membrane immunoglobulin; neuronal Wiskott–Aldrich syndrome protein; phosphatidylinositol-3 kinase; phosphatidylinositol-3,4,5-triphosphate; phospholipase Cγ2; slingshot phosphatase.
© 2013.