CD79B, in conjunction with CD79A, constitutes an indispensable component of the B-cell receptor (BCR) complex, essential for the transduction of signals necessary for B-cell activation, development, and differentiation. This heterodimer acts as a pivotal conduit for conveying extracellular antigen recognition signals to the intracellular signaling apparatus of B-cells, thereby initiating a cascade of events leading to B-cell proliferation, antibody production, and the establishment of immunological memory. The function of CD79B extends beyond mere signal transduction; it is crucial for the surface expression of the BCR complex, ensuring that B-cells are capable of responding to antigens with high sensitivity and specificity. This sensitivity is paramount for the adaptive immune system's ability to identify and neutralize a vast array of pathogens, highlighting CD79B's role in maintaining the immunological repertoire and safeguarding organismal health.
The activation of CD79B is intricately linked to its phosphorylation status, which occurs upon antigen binding to the BCR, triggering a series of phosphorylation events on the immunoreceptor tyrosine-based activation motifs (ITAMs) present in the cytoplasmic tails of CD79B. This phosphorylation serves as a critical signal for the recruitment and activation of downstream signaling molecules, including Syk kinase, which further propagates the signal through various pathways, such as PLCγ2, leading to calcium mobilization, cytoskeletal reorganization, and transcriptional activation of genes involved in B-cell proliferation and differentiation. Moreover, the modulation of CD79B activity and its expression levels are finely tuned by the cellular context, ensuring that B-cell activation is appropriately regulated in response to immunological challenges. This regulation involves a complex interplay of co-stimulatory signals and inhibitory checkpoints that ensure the immune response is effective against pathogens. Understanding the mechanisms underlying CD79B activation offers profound insights into the orchestration of B-cell functions and the broader dynamics of the immune response.
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