Continuous signaling of CD79b and CD19 is required for the fitness of Burkitt lymphoma B cells
He X, Kläsener K, Iype JM, Becker M, Maity PC, Cavallari M, Nielsen PJ, Yang J, Reth M.
Expression of the B cell antigen receptor (BCR) is essential not only for the development but also for the maintenance of mature B cells. Similarly, many B cell lymphomas including Burkitt lymphoma (BL), require continuous BCR signaling for their tumor growth. This growth is driven by immunoreceptor tyrosine-based activation motif (ITAM) and PI3 kinase (PI3K) signaling. Here, we employ CRISPR/Cas9 to delete BCR and B cell coreceptor genes in the human BL cell line Ramos. We find that Ramos B cells require the expression of the BCR signaling component Igβ (CD79b), and the co-receptor CD19, for their fitness und competitive growth in culture. Furthermore, we show that in the absence of any other BCR component, Igβ can be expressed on the B cell surface, where it is found in close proximity to CD19 and signals in an ITAM-dependent manner. These data suggest that Igβ and CD19 are part of an alternative B cell signaling module that use continuous ITAM/PI3K signaling to promote the survival of B lymphoma and normal B cells.
