Abstract
The signal through the B-cell antigen-receptor (BCR) complex, which is composed of the BCR itself and the Igα (CD79a)/Igβ (CD79b) heterodimer, is essential for B-cell development and humoral immune responses. The cytoplasmic domains of both Igα and Igβ have an ITAM (immunoreceptor tyrosine-based activation motif), and tyrosine residues in the ITAM are phosphorylated after BCR stimulation followed by the recruitment and activation of protein tyrosine kinases (PTKs). Two classes of the BCR-associated PTK are now defined: Src-PTK such as Lyn, Fyn, Blk, Lck [1–3], and spleen tyrosine kinase, Syk.
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Kurosaki, T., Lowell, C.A. (2012). Establishment of a Novel System for Studying the Syk Function in B Cells. In: Shibasaki, M., Iino, M., Osada, H. (eds) Chembiomolecular Science. Springer, Tokyo. https://doi.org/10.1007/978-4-431-54038-0_17
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DOI: https://doi.org/10.1007/978-4-431-54038-0_17
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