| First Author | Low MSY | Year | 2019 |
| Journal | Cell Rep | Volume | 29 |
| Issue | 9 | Pages | 2634-2645.e5 |
| PubMed ID | 31775034 | Mgi Jnum | J:297545 |
| Mgi Id | MGI:6472094 | Doi | 10.1016/j.celrep.2019.10.097 |
| Citation | Low MSY, et al. (2019) IRF4 Activity Is Required in Established Plasma Cells to Regulate Gene Transcription and Mitochondrial Homeostasis. Cell Rep 29(9):2634-2645.e5 |
| abstractText | The transcription factor interferon regulatory factor 4 (IRF4) is critical for the development, maintenance, and function of plasma cells. The mechanism by which IRF4 exerts its action in mature plasma cells has been elusive due to the death of all such cells upon IRF4 loss. While we identify apoptosis as a critical pathway for the death of plasma cells caused by IRF4 loss, we also determine that IRF4 did not regulate the intrinsic apoptotic pathway directly. By using an inducible IRF4 deletion system in the presence of the overexpression of anti-apoptotic BCL2, we identify genes whose expression is coordinated by IRF4 and that in turn specify plasma cell identity and mitochondrial homeostasis. |
