INDUCTION OF THE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR (CSF) RECEPTOR BY GRANULOCYTE CSF INCREASES THE DIFFERENTIATIVE OPTIONS OF A MURINE HEMATOPOIETIC PROGENITOR-CELL

被引:52
|
作者
KREIDER, BL
PHILLIPS, PD
PRYSTOWSKY, MB
SHIRSAT, N
PIERCE, JH
TUSHINSKI, R
ROVERA, G
机构
[1] WISTAR INST,36 & SPRUCE,PHILADELPHIA,PA 19104
[2] HOSP UNIV PENN,DEPT PATHOL,PHILADELPHIA,PA 19104
[3] NCI,CELLULAR & MOLEC BIOL LAB,BETHESDA,MD 20892
[4] IMMUNEX CORP,SEATTLE,WA 98101
关键词
D O I
10.1128/MCB.10.9.4846
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
32DCl3(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 32DCl3(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.
引用
收藏
页码:4846 / 4853
页数:8
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