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作 者:刘歆荣[1] 周柔丽[1] 张青云 张页[1] 邵根泽[1] 金月英[1] 张莎[1] 林明[1] 芮静安[3] 叶大雄[3]
机构地区:[1]北京大学基础医学院细胞生物学与遗传学系,北京100083 [2]北京大学临床肿瘤学院 [3]北京协和医院
出 处:《北京大学学报(医学版)》2003年第4期340-347,共8页Journal of Peking University:Health Sciences
基 金:教育部教育振兴行动计划特殊专项 ("九八五"工程 );北京市"2 48重大创新工程"科技计划项目资助~~
摘 要:目的 :鉴定由肝细胞癌 (HCC)相关新基因LAPTM 4B编码的蛋白质并研究其生物学特性。方法 :以Westernblot、免疫组化及双向电泳鉴定新基因的表达产物 ;以免疫共沉淀等方法研究分子间的相互作用。结果 :LAPTM4B基因编码相对分子质量分别为 35× 10 3 和 2 4× 10 3 、等电点分别为 9.0 7和 4 .6 5的两种异型分子。它们在肝癌组织及肝癌细胞系的表达显著上调 ,而相对分子质量为 35× 10 3 者尤为明显 ,并与细胞分化程度相关。LAPTM4B蛋白可与整合素α 6亚单位及表皮生长因子 (EGF)受体形成信号复合物。结论 :LAPTM4B 35蛋白在人肝癌组织及细胞系过表达 ,并可能通过与细胞表面的整合素受体及EGF受体形成复合物而参与细胞外基质成分所启动的信号转导。Objective: To identify and characterize the novel proteins encoded by a HCC associated novel gene, LAPTM4B (lysosomeassociated protein transmembrane 4 beta). Methods: The novel proteins was identified by Western blot,immunohistochemistry and 2D electrophoresis; the molecular interactions were studied by co immunoprecipitation. Results: LAPTM4B encoded two isoforms of proteins with molecular weight 35×10 3 and 24×10 3 and pI 9.07 and 4.65, respectively. The expression levels of LAPTM4B proteins in HCC tissues and cell lines were upregulated and related to differentiation, and most dramatically raised for 35×10 3 one. It was demonstrated that LAPTM4B-integrin α6 and LAPTM4B-EGFR signaling complexes were formed when BEL 7402 cells were seeded on laminin substrate. Conclusion: The LAPTM4B 35 protein is overexpressed in human HCC tissues and cell lines and may involve in signal transduction triggered by extracellular matrix via interaction with integrin α6 and EGFR on cell surface.
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