The role of soluble growth factors in inducing transient growth and clonal extinction of stroma cell dependent erythroblastic leukemia cells

被引:17
作者
Itoh, K
Friel, J
Laker, C
Zeller, W
Just, U
Bittner, S
Nibbs, RJB
Harrison, PR
Nishikawa, SI
Mori, KJ
Ostertag, W
机构
[1] UNIV HAMBURG, HEINRICH PETTE INST EXPT VIROL & IMMUNOL, D-20251 HAMBURG, GERMANY
[2] UNIV HAMBURG, KRANKENHAUS EPPENDORF, MED CLIN 2, DEPT HEMATOL & ONCOL, D-2000 HAMBURG, GERMANY
[3] BEATSON INST CANC RES, CANC RES CAMPAIGN, BEATSON LABS, GLASGOW G61 1BD, LANARK, SCOTLAND
[4] KYOTO UNIV, FAC MED, DEPT CLIN MOL BIOL, KYOTO, JAPAN
[5] NIIGATA UNIV, FAC SCI, DEPT BIOL, NIIGATA 95021, JAPAN
基金
英国医学研究理事会;
关键词
apoptosis; clonal extinction; erythropoiesis; stem cell factor; stroma cells;
D O I
10.1038/sj.leu.2400787
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A coculture system of a murine erythroblastic leukemia cell line (ELM-D) with its supportive stromal cell line (MS-5) was established. Long-term growth of ELM-D cells is strictly stroma cell dependent. Interaction between stem cell factor (SCF) and its receptor, c-kit, was demonstrated to be important for stroma cell-dependent growth by anti c-kit neutralizing monoclonal antibody (mAb) inhibition experiments. Significantly, soluble growth factors such as granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-3 (IL-3) or SCF of MS-5 stromal cells (MS-5 CM) could replace the requirement of stroma cells for a considerable period. However, ELM-D cells maintained in these growth factors underwent clonal extinction after 3-6 weeks unless contact with stroma was re-established. Furthermore, IL-3 or GM-CSF acted in a dominant manner in inducing cell death in the presence of stroma cells. Cells showing clonal extinction undergo programmed cell death and do not differentiate. These altered growth properties of ELM-D cells exposed to soluble growth factors or to stroma cells appear to be analogous to those described for T or B cells primed by antigen presenting cells and then grown in growth factors.
引用
收藏
页码:1753 / 1761
页数:9
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