Department of Pediatric Hematology/Oncology, Hannover Medical School, Hannover, Germany.
PLoS One. 2007 Mar 21;2(3):e306. doi: 10.1371/journal.pone.0000306.
Hematopoietic stem cell differentiation is specified by cytokines and transcription factors, but the mechanisms controlling instructive and permissive signalling networks are poorly understood. We provide evidence that CLP1-dependent IL7-receptor mediated B cell differentiation is critically controlled by the transcriptional repressor Gfi1. Gfi1-deficient progenitor B cells show global defects in IL7Ralpha-dependent signal cascades. Consequently, IL7-dependent trophic, proliferative and differentiation-inducing responses of progenitor B cells are perturbed. Gfi1 directly regulates expression levels of IL7Ralpha and indirectly controls STAT5 signalling via expression of SOCS3. Thus, Gfi1 selectively specifies IL7-dependent development of B cells from CLP1 progenitors, providing clues to the transcriptional networks integrating cytokine signals and lymphoid differentiation.
造血干细胞的分化由细胞因子和转录因子决定,但控制指令性和许可性信号网络的机制还了解甚少。我们提供的证据表明,CLP1 依赖性的 IL7 受体介导的 B 细胞分化受到转录抑制因子 Gfi1 的严格控制。缺乏 Gfi1 的祖细胞 B 细胞在 IL7Ralpha 依赖性信号级联中表现出全局性缺陷。因此,IL7 依赖性的祖细胞的营养、增殖和诱导分化反应受到干扰。Gfi1 直接调节 IL7Ralpha 的表达水平,并通过表达 SOCS3 间接控制 STAT5 信号。因此,Gfi1 选择性地规定了 CLP1 祖细胞中 IL7 依赖性 B 细胞的发育,为整合细胞因子信号和淋巴样分化的转录网络提供了线索。