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作 者:霍寅萍[1] 储著朗[1] 余科科[1] 郑红[1] 瞿成奎[1] 汪思应[1]
机构地区:[1]安徽医科大学病理生理学教研室,合肥230032
出 处:《安徽医科大学学报》2010年第5期593-596,共4页Acta Universitatis Medicinalis Anhui
基 金:国家自然科学基金(编号:30873046)
摘 要:目的研究SHP-2酪氨酸磷酸酶激活突变的肥大细胞对白细胞素3(IL3)呈高增殖敏感性的机制。方法从野生型(WT组)、SHP-2杂合突变型(SHP-2D61G/+)小鼠骨髓中获取髓系细胞,运用细胞集落形成实验观察髓系细胞集落形成能力,用不同剂量的IL30、0.2、2.0、10.0ng/ml)诱导比较两组髓系细胞形成集落数的差异。从髓系细胞中分离培养出肥大细胞,MTS法观察肥大细胞在IL3诱导下的细胞增殖性,Westernblot比较肥大细胞中Erk、Akt的表达及磷酸化水平,免疫共沉淀和Westernblot检测肥大细胞中SHP-2与Gab2结合能力。结果 SHP-2D61G/+组比WT组的髓系细胞集落形成能力增强;IL3诱导下的肥大细胞在SHP-2D61G/+组显示了更高的增殖活性;SHP-2D61G/+组肥大细胞中Erk和Akt的磷酸化水平较WT组明显升高;SHP-2D61G/+杂合突变后与Gab2结合能力增高。结论 SHP-2D61G/+的肥大细胞对IL3呈高增殖敏感性,其分子机制可能与SHP-2D61G/+与Gab2的结合能力增强,从而进一步参与对IL3介导的Ras-Erk、PI3K-Akt信号通路的正调控作用有关。Objective To study the mechanism of the mast cell of activating mutant SHP-2 tyrosine phosphatase shows high proliferation sensitivity to IL3. Methods Myeloid cells were obtained from marrow of WT and SHP-2D61G/ + mutant mice. The colony-forming assay( CFA) was used to observe the colony-forming ability of myeloid cells,and compared the colony-forming ability of two kinds of myeloid cells under different doses of IL3( 0,0. 2, 2. 0,10. 0 ng/ml) . Mast cells were isolated and cultured from myeloid cells,and MTS assay was used to observe different proliferation of mast cells to IL3 . Western bolt was applied to exam the expression and phosphorylation of Erk and Art in the mast cells,and immunoprecipitation were used to exam the binding capacity of SHP-2 with Gab-2. Results The colony-forming ability of bone marrow cells increased and the proliferative of bone marrow-derived mast cells to IL3 were more obviously in the SHP-2D61G/ + than in the WT. The phosphorylation level of Erk and Akt was higher in the SHP-2D61G/ + than in the WT. The binding capacity of SHP-2D61G/ + with Gab2 improved obviously. Conclusion The bone marrow-derived mast cells shows the high sensitivity to IL3 in the SHP-2D61G/ + . The molecular mechanism may be associated with SHP-2D61G/ + promotes the binding ability of Gab2,and further participates in the IL3-mediated Ras-Erk,PI3K-Akt signaling pathways.
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