Nf1 regulates hematopoietic progenitor cell growth and Ras signaling in response to multiple cytokines

被引:124
作者
Zhang, YY
Vik, TA
Ryder, JW
Srour, EF
Jacks, T
Shannon, K
Clapp, DW
机构
[1] Indiana Univ, Sch Med, Dept Pediat, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46202 USA
[4] Indiana Univ, Sch Med, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[5] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
[6] MIT, Canc Res Ctr, Cambridge, MA 02139 USA
[7] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
关键词
neurofibromin; hematopoietic progenitor; cytokines; Ras; granulocyte/macrophage colony-stimulating factor;
D O I
10.1084/jem.187.11.1893
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neurofibromin, the protein encoded by the NF1 tumor-suppressor gene, negatively regulates the output of p21(ras) (Ras) proteins by accelerating the hydrolysis of active Ras-guanosine triphosphate to inactive Ras-guanosine diphosphate. Children with neurofibromatosis type 1 (NF1) are predisposed to juvenile chronic myelogenous leukemia (JCML) and other malignant myeloid disorders, and heterozygous Nf1 knockout mice spontaneously develop a myeloid disorder that resembles JCML. Both human and murine leukemias show loss of the normal allele. JCML cells and Nf1(-/-) hematopoietic cells isolated from fetal livers selectively form abnormally high numbers of colonies derived from,granulocyte-macrophage progenitors in cultures supplemented with low concentrations of granulocyte-macrophage colony stimulating factor (GMCSF). Taken together, these data suggest that neurofibromin is required to downregulate Ras activation in myeloid cells exposed to GM-CSF. We have investigated the growth and proliferation of purified populations of hematopoietic progenitor cells isolated from Nf1 knockout mice in response to the cytokines interleukin (IL)-3 and stem cell factor (SCF), as well as to GM-CSF. We found abnormal proliferation of both immature and lineage-restricted progenitor populations, and we observed increased synergy between SCF and either IL-3 or GM-CSF in Nf1(-/-) progenitors. Nf1(-/-) fetal livers also showed an absolute increase in the numbers of immature progenitors, We further demonstrate constitutive activation of the Ras-Raf-MAP (mitogen-activated protein) kinase signaling pathway in primary c-kit(+) Nf1(-/-) progenitors and hyperactivation of MAP kinase after growth factor stimulation. The results of these experiments in primary hematopoietic cells implicate Nf1 as playing a central role in regulating the proliferation and survival of primitive and lineage-restricted myeloid progenitors in response to multiple cytokines by modulating Ras output.
引用
收藏
页码:1893 / 1902
页数:10
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