| First Author | Kallies A | Year | 2011 |
| Journal | Blood | Volume | 117 |
| Issue | 6 | Pages | 1869-79 |
| PubMed ID | 21131593 | Mgi Jnum | J:169573 |
| Mgi Id | MGI:4941294 | Doi | 10.1182/blood-2010-08-303123 |
| Citation | Kallies A, et al. (2011) A role for Blimp1 in the transcriptional network controlling natural killer cell maturation. Blood 117(6):1869-79 |
| abstractText | Natural killer (NK) cells are innate lymphocytes capable of immediate effector functions including cytokine production and cytotoxicity. Compared with B and T cells, the factors that control the peripheral maturation of NK cells are poorly understood. We show that Blimp1, a transcriptional repressor required for the differentiation of plasma cells and short-lived effector T cells, is expressed by NK cells throughout their development. Interleukin 15 (IL-15) is required for the early induction of Blimp1 in NK cells, with expression increasing in the most mature subsets of mouse and human NK cells. We show that Blimp1 is required for NK-cell maturation and homeostasis and for regulating their proliferative potential. It is also essential for high granzyme B expression, but not for most cytokine production and cytotoxicity. Surprisingly, interferon regulatory factor 4 (IRF4) and B-cell lymphoma 6 (Bcl6), 2 transcription factors crucial for the regulation of Blimp1 in B and T cells, are largely dispensable for Blimp1 expression in NK cells. T-bet deficiency, however, leads to attenuated Blimp1 expression. We have identified NK cells as the first hematopoietic cell type in which the IRF4-Blimp1-Bcl6 regulatory axis is not in operation, highlighting the distinct nature of the NK-cell gene-regulatory network. |
