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作 者:张宁[1] 胡志毅[1] 殷国勇[1] 范卫民[1] 陶松年[1] 王道新[1] 董天华[2]
机构地区:[1]南京医科大学第一附属医院骨科,210029 [2]苏州大学附属第一医院骨科
出 处:《中华创伤骨科杂志》2006年第9期846-851,共6页Chinese Journal of Orthopaedic Trauma
基 金:南京医科大学第一附属医院引进人才基金(599NA0502)
摘 要:目的探索G蛋白耦联受体激酶结合蛋白1(GITI)在成骨细胞迁移中的作用,并分析其机理。方法通过Western blot方法检测GIT1蛋白在鼠的成骨细胞内的表达;用免疫荧光染色方法确定:在血小板衍生生长因子(PDGF)不刺激和刺激的条件下,GIT1和细胞外调节激酶1/2(ERK1/2)在成骨细胞内的位置;用共同免疫沉淀的方法测定GIT1和ERK1/2相互结合,并且用免疫荧光双染的方法确定这两种蛋白相互结合的位置;用包含GIT1-RNA发夹结构的腺病毒感染成骨细胞后,用免疫荧光染色方法确定磷酸化ERK1/2(pERK1/2)在成骨细胞内的位置,用划痕愈合法检测在PDGF刺激下的迁移能力。结果在成骨细胞内,PDGF刺激导致了GIT1和ERK1/2的相互结合,并且这种结合发生在成骨细胞的局部粘附内。包含GIT1-RNA发夹结构的腺病毒明显抑制了pERK1/2招募至成骨细胞局部粘附内以及PDGF所刺激的成骨细胞的迁移。结论在PDGF刺激下,GIT1招募pERK1/2至成骨细胞的局部粘附内,从而促进成骨细胞的迁移。Objective To study the function and mechanism of GIT1 (G protein coupled receptor kinase interacting protein 1) in osteoblast migration. Methods GIT1 and ERK1/2 (Extracellular Signal-regulated kinase 1/2) were detected in mice primary osteoblasts. The localizations of GIT1 and ERK1/2 were determined by immunofluorescence stain with or without PDGF (platelet-derived growth factor) stimulation. The association of GIT1 and ERK1/2 was analyzed by co-immunoprecipitation and western blot. After stimulation, the co-localization of GIT1 and pERK1/2 in osteoblasts was detected by double-immunofluorescence stain. The pERK1/2 localization was detected by immunofluorescence stain after GIT1 RNAh adenovirns infection of osteoblasts. The role of this association was determined by wound healing assay. Results The co-immunoprecipitation results showed that GIT1 interacted with ERK1/2 in osteoblasts induced by PDGF and this association occurred in focal adhesions. GIT1 RNAh adenovirus significantly inhibited the pERK1/2 translocation to focal adhesions and osteoblast migration induced by PDGF. Conclusion GIT1 associates with ERK1/2 in osteoblasts, which is required for pERK1/2 translocation to focal adhesions and osteoblast migration.
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