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国家重点基础研究发展计划(2009CB521706)

作品数:4 被引量:21H指数:2
相关作者:韩骅项捷秦鸿雁尹郸丹刘强更多>>
相关机构:第四军医大学第四军医大学唐都医院更多>>
发文基金:国家重点基础研究发展计划国家自然科学基金广东省自然科学基金更多>>
相关领域:生物学自动化与计算机技术医药卫生更多>>

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PAQR膜蛋白家族研究进展被引量:2
2012年
孕激素和脂联素分子受体家族(PAQRs)是一类不同于G蛋白耦联受体家族的7次跨膜蛋白家族,目前发现该家族在人类具有11个成员。这类蛋白的结构类似于细菌的溶血素蛋白III,跨膜区域完全由一个高度保守的PFAM-UPF0073结构域构成。对该家族成员的生理功能研究发现,PAQR1,PAQR2具有维持代谢稳态和参与炎症反应的作用。PAQR5,PAQR7,PAQR8对于精子顶体反应,卵细胞的成熟和细胞凋亡有着重要的调节作用。随着对该家族成员分子的深入研究,一方面将更新对其现有生理病理过程的认识,另一方面将更加明确该类蛋白介导的信号转导通路,为相关疾病的治疗提供新的靶点和新的策略。
项捷秦鸿雁韩骅
关键词:脂联素受体
miR-124 suppresses multiple steps of breast cancer metastasis by targeting a cohort of pro-metastatic genes in vitro被引量:6
2011年
Metastasis is a multistep process involving modification of morphology to suit migration, reduction of tumor cell adhesion to the extracellular matrix, increase of cell mobility, tumor cell resistance to anoikis, and other steps. MicroRNAs are well-suited to regulate tumor metastasis due to their capacity to repress numerous target genes in a coordinated manner, thereby enabling their intervention at multiple steps of the invasion-metastasis cascade. In this study, we identified a microRNA exemplifying these attributes, miR-124, whose expression was reduced in aggressive MDA-MB-231 and SK-3rd breast cancer cells. Down-regulation of miR-124 expression in highly aggressive breast cancer cells contributed in part to DNA hypermethylation around the promoters of the three genes encoding miR-124. Ectopic expression of miR-124 in MDA-MB-231 cells suppressed metastasis-related traits including formation of spindle-like morphology, migratory capacity, adhesion to fibronectin, and anoikis. These findings indicate that miR-124 suppresses multiple steps of metastasis by diverse mechanisms in breast cancer cells and suggest a potential application of miR-124 in breast cancer treatment.
Xiao-Bin LvYu JiaoYanwei QingHaiyan HuXiuying CuiTianxin LinErwei SongFengyan Yu
关键词:纤维连接蛋白
人H-Ras12V突变蛋白表达载体的构建及表达
2009年
目的:构建研究H-Ras12V突变蛋白的表达载体,并在体外进行表达和检测.方法:从细胞中分离提取RNA,通过RT-PCR扩增获得人的正常H-RascDNA,测序鉴定.通过PCR介导的定向突变的方法,在其第12位氨基酸处引入一个错义突变G→V,连入测序载体进行鉴定.应用DNA重组技术,将获得的H-Ras12VcDNA插入真核表达载体pEGFP-C2,使用限制性酶切反应鉴定.通过脂质体将重组质粒转染入Hela细胞,使用Western Blot对其融合蛋白进行检测.结果:经过XhoI和BamHI的双酶切以及测序鉴定证实成功构建了pEGFP-H-Ras12V融合蛋白表达载体,克隆基因与GenBank登陆结果一致并成功实现其第12位氨基酸G→V的突变.WesternBlot证实融合蛋白特异性表达,并在转染的细胞系中观察到绿色荧光蛋白的表达.结论:成功构建了pEG-FP-H-Ras12V融合蛋白的表达载体,并在体外鉴定EGFP-H-Ras12V融合蛋白的表达.
胡昳旸梁亮尹郸丹刘强韩骅
关键词:融合蛋白
The Notch signaling pathway in retinal dysplasia and retina vascular homeostasis被引量:13
2010年
The retina is one of the most essential elements of vision pathway in vertebrate. The dysplasia of retina cause congenital blindness or vision disability in individuals, and the misbalance in adult retinal vascular homeostasis leads to neo adults, such as diabetic retinopathy or age-related macular degeneration. Many developmental signaling pathways are involved in the process of retinal development and vascular homeostasis. Among them, Notch signaling pathway has long been studied, and Notch signaling-interfered mouse models show both neural retina dysplasia and vascular abnormality. In this review, we discuss the roles of Notch signaling in the maintenance of retinal progenitor cells, specification of retinal neurons and glial cells, and the sustaining of retina vascular homeostasis, especially from the aspects of conditional knockout mouse models. The potential of Notch signal manipulation may provide a powerful cell fate- and neovascularization-controUing tool that could have important applications in treatment of retinal diseases.
Minhua ZhengZifeng ZhangXingcheng ZhaoYuqiang DingHua Han
关键词:NEOVASCULARIZATION
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