Meierhoff G, Dehmel U, Gruss H J, Rosnet O, Birnbaum D, Quentmeier H, Dirks W, Drexler H G
German Collection of Microorganisms and Cell Cultures, Braunschweig.
Leukemia. 1995 Aug;9(8):1368-72.
The FLT3 gene encodes a receptor tyrosine kinase that is closely related to two well-known receptors, KIT and FMS, that regulate with their respective ligands, stem cell factor (SCF) and macrophage colony-stimulating factor (M-CSF), proliferation and differentiation of hematopoietic cells. The ligand for FLT3, FL, is active in both soluble and membrane-bound forms. We examined expression of FL and FLT3 mRNA in a panel of some 110 continuous human leukemia-lymphoma cell lines from all major hematopoietic cell lineages by Northern blot analysis. FLT3 mRNA is expressed primarily in pre-B cell lines, myeloid and monocytic cell lines whereas FL mRNA was detected in most cell lines from all cell lineages. Analysis of FLT3 receptor protein expression examined with a specific anti-FLT3 monoclonal antibody and flow cytometry in 17 cell lines confirmed the results obtained at the mRNA level. Forty of 110 cell lines displayed both receptor and ligand mRNA suggesting a possible autocrine or intracrine stimulation. In normal hematopoietic cells expression of FLT3 was reported to be associated with CD34 positivity, a cell surface marker of immature and precursor cells. No correlation between FLT3 and CD34 expression was found in the cell lines analyzed. These studies served to illustrate further the importance of the FL-FLT3 ligand-receptor system in the regulation of hematopoietic cells.
FLT3基因编码一种受体酪氨酸激酶,它与两种著名的受体KIT和FMS密切相关,这两种受体分别通过其各自的配体干细胞因子(SCF)和巨噬细胞集落刺激因子(M-CSF)来调节造血细胞的增殖和分化。FLT3的配体FL,以可溶性和膜结合形式均具有活性。我们通过Northern印迹分析检测了约110种来自所有主要造血细胞谱系的连续人白血病-淋巴瘤细胞系中FL和FLT3 mRNA的表达。FLT3 mRNA主要在pre-B细胞系、髓系和单核细胞系中表达,而FL mRNA在所有细胞谱系的大多数细胞系中均有检测到。用特异性抗FLT3单克隆抗体和流式细胞术对17种细胞系进行FLT3受体蛋白表达分析,证实了在mRNA水平获得的结果。110种细胞系中有40种同时显示受体和配体mRNA,提示可能存在自分泌或细胞内刺激。据报道,在正常造血细胞中,FLT3的表达与CD34阳性相关,CD34是未成熟和前体细胞的一种细胞表面标志物。在所分析的细胞系中未发现FLT3与CD34表达之间存在相关性。这些研究进一步说明了FL-FLT3配体-受体系统在造血细胞调节中的重要性。