间质细胞
干细胞因子
生物
基质
造血
细胞生物学
促红细胞生成素
干细胞
生长因子
祖细胞
骨髓
癌症研究
免疫学
受体
内分泌学
生物化学
免疫组织化学
作者
Jim O’Prey,Nicholas R. Leslie,Katsukiko Itoh,Wolfram Ostertag,Chris Bartholomew,Paul R. Harrison
出处
期刊:Blood
[Elsevier BV]
日期:1998-03-01
卷期号:91 (5): 1548-1555
被引量:14
标识
DOI:10.1182/blood.v91.5.1548.1548_1548_1555
摘要
Defining how the stromal requirements of hematopoietic progenitors change during leukemia progression is an important topic that is not well understood at present. The murine ELM erythroleukemia is an interesting model because the erythroid progenitors retain dependence on bone marrow-derived stromal cells for long-term growth in vitro, and they also undergo erythroid differentiation in the presence of erythropoietin (EPO) and interleukin-3 (IL-3). In this report, we have shown using neutralizing antibodies that stem cell factor (SCF), insulin-like growth factor (IGF)-1, and integrin signaling pathways are all involved. We then determined whether ELM cells can be maintained long-term without stroma in various combinations of growth factors produced by stroma cells or growth factors for which ELM cells have receptors. This showed that ELM cells could be maintained with high efficiency in SCF alone; furthermore, the cells remained absolutely SCF-dependent and did not become more tumorigenic than cells maintained on stroma. In contrast, ELM cells underwent clonal extinction when serially cloned in IGF1; any cells that survived long-term growth in IGF-1 were found to be IGF1-independent. One important difference between maintaining ELM cells on stroma and growth in SCF is that stroma reversibly inhibits their differentiation in response to EPO and IL-3, whereas SCF does not.
科研通智能强力驱动
Strongly Powered by AbleSci AI