| First Author | Hayashi K | Year | 2003 |
| Journal | Immunity | Volume | 18 |
| Issue | 6 | Pages | 825-36 |
| PubMed ID | 12818163 | Mgi Jnum | J:84040 |
| Mgi Id | MGI:2664645 | Doi | 10.1016/s1074-7613(03)00142-0 |
| Citation | Hayashi K, et al. (2003) Distinct signaling requirements for Dmu selection, IgH allelic exclusion, pre-B cell transition, and tumor suppression in B cell progenitors. Immunity 18(6):825-36 |
| abstractText | The pre-B cell receptor triggers expansion and differentiation of pre-B cells (the pre-B cell transition), as well as inhibition of V(H) to DJ(H) recombination (allelic exclusion). The latter also accounts for counter-selection of pro-B cells expressing Dmu protein (Dmu selection). However, the signaling pathways responsible for these events remain poorly defined. Here we show complete arrest of B cell development at the pre-B cell transition in BASH/CD19 double mutant mice, indicating partial redundancy of the two B cell-specific adaptors. Allelic exclusion remained intact in the double mutant mice, whereas Dmu selection was abolished in BASH mutant mice. Thus, distinct signals are required for these events. In addition, both mutant mice succumbed to pre-B cell leukemia, indicating that BASH and CD19 contribute to tumor suppression. |
