Kreider B L, Phillips P D, Prystowsky M B, Shirsat N, Pierce J H, Tushinski R, Rovera G
Wistar Institute, Philadelphia, Pennsylvania 19104.
Mol Cell Biol. 1990 Sep;10(9):4846-53. doi: 10.1128/mcb.10.9.4846-4853.1990.
32DC13(G) is an interleukin-3-dependent murine hematopoietic precursor cell line which differentiates into neutrophilic granulocytes upon exposure to granulocyte colony-stimulating factor (G-CSF) but ceases to proliferate and dies when exposed to granulocyte-macrophage (GM)-CSF. Surface receptors for GM-CSF are undetectable on 32DC13(G) cells but can be induced by priming the cells with G-CSF. Exposure of the G-CSF-primed cells to GM-CSF then results in the generation of monocytes as well as granulocytes. The acquired competence to respond to GM-CSF remains irreversibly encoded in the primed cells, although the GM-CSF receptor can be down regulated by interleukin-3. This phenomenon suggests a mechanism by which hematopoietic precursors may obtain additional receptors, thereby increasing their differentiative potential.
32DC13(G)是一种依赖白细胞介素-3的小鼠造血前体细胞系,在暴露于粒细胞集落刺激因子(G-CSF)时可分化为嗜中性粒细胞,但在暴露于粒细胞-巨噬细胞(GM)-CSF时停止增殖并死亡。GM-CSF的表面受体在32DC13(G)细胞上无法检测到,但可以通过用G-CSF预处理细胞来诱导。将经G-CSF预处理的细胞暴露于GM-CSF会导致单核细胞以及粒细胞的生成。尽管GM-CSF受体可被白细胞介素-3下调,但对GM-CSF产生反应的获得性能力仍不可逆地编码在预处理细胞中。这一现象提示了一种造血前体可能获得额外受体从而增加其分化潜能的机制。