Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, Rome, Italy.
Cell Death Differ. 2011 Feb;18(2):371-80. doi: 10.1038/cdd.2010.110. Epub 2010 Sep 10.
Stem cell factor (SCF), the ligand for the c-kit receptor, is essential for the production of red blood cells during development and stress erythropoiesis. SCF promotes erythroblast proliferation and survival, while delaying erythroid differentiation through mechanisms that are largely unknown. In cultures of primary human differentiating erythroblasts, we found that SCF induces an increase in the expression of Notch2, a member of the Notch family implicated in the control of cell growth and differentiation. Functional inhibition of either Notch or its ligand Jagged1 inhibited the effects of SCF on erythroid cell expansion. SCF also induced the expression of Hes-1 and GATA-2, which may contribute to transduce Notch2 signals in response to SCF. Transduction of primary erythroid precursors with a dominant-negative Notch2 mutant inhibited both basal and SCF-mediated erythroblast expansion, and counteracted the effects of SCF on erythroblast differentiation. These findings provide a clue to understand the effects of increased proliferation and delayed differentiation elicited by SCF on the erythroid compartment and indicate Notch2 as a new player in the regulation of red cell differentiation.
干细胞因子 (SCF) 是 c-kit 受体的配体,对于发育过程中和应激状态下的红细胞生成至关重要。SCF 通过尚未完全明确的机制促进红系母细胞的增殖和存活,同时延迟其分化。在原代人红细胞分化培养中,我们发现 SCF 诱导 Notch2 表达增加, Notch2 是 Notch 家族的一个成员,与细胞生长和分化的控制有关。Notch 或其配体 Jagged1 的功能抑制均可抑制 SCF 对红细胞扩增的影响。SCF 还诱导 Hes-1 和 GATA-2 的表达,这可能有助于 Notch2 信号转导以响应 SCF。用显性负 Notch2 突变体转导原代红细胞前体可抑制基础和 SCF 介导的红系母细胞扩增,并抵消 SCF 对红系母细胞分化的影响。这些发现为理解 SCF 对红细胞系增殖增加和分化延迟的影响提供了线索,并表明 Notch2 是红细胞分化调控的新成员。