Koay Debbie C, Nguyen Tr- Hung, Sartorelli Alan C
Department of Pharmacology and Developmental Therapeutics Program, Cancer Center, New Haven, CT 06520, USA.
Cell Signal. 2002 Mar;14(3):239-47. doi: 10.1016/s0898-6568(01)00237-6.
The granulocyte colony-stimulating factor receptor (G-CSFR) regulates the proliferation, differentiation and survival of neutrophilic progenitor cells. In these studies, we introduced mutant G-CSFRs with cytoplasmic domains truncated approximately every 30 amino acids from the C-terminus into interleukin-3 (IL-3)-dependent myeloid LGM-1 cells. The G-CSFR membrane proximal region containing the Box 2 homology sequence was determined to be critical for proliferative signaling, as well as for activation of Janus kinase (JAK2) and p44/42 mitogen-activated protein kinase (MAPK) following G-CSF stimulation. In the presence of increasing concentrations of JAK2 or p44/42 MAPK inhibitors, LGM-1 cells expressing the full-length G-CSFR exhibited a decreased capacity to proliferate in response to G-CSF. These results demonstrate that JAK2 and p44/42 MAPK activation is involved in proliferative signaling through the G-CSFR membrane proximal region containing the Box 2 homology sequence.
粒细胞集落刺激因子受体(G-CSFR)调节嗜中性祖细胞的增殖、分化和存活。在这些研究中,我们将细胞质结构域从C末端开始大约每隔30个氨基酸截断的突变型G-CSFR导入依赖白细胞介素-3(IL-3)的髓系LGM-1细胞中。含有Box 2同源序列的G-CSFR膜近端区域被确定对增殖信号传导至关重要,对G-CSF刺激后Janus激酶(JAK2)和p44/42丝裂原活化蛋白激酶(MAPK)的激活也至关重要。在JAK2或p44/42 MAPK抑制剂浓度增加的情况下,表达全长G-CSFR的LGM-1细胞对G-CSF作出反应的增殖能力下降。这些结果表明,JAK2和p44/42 MAPK的激活通过含有Box 2同源序列的G-CSFR膜近端区域参与增殖信号传导。