生物化学与生物物理进展
生物化學與生物物理進展
생물화학여생물물리진전
PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS
2009年
11期
1423-1428
,共6页
刘宇明%彭智%邓唯唯%石太平%马大龙
劉宇明%彭智%鄧唯唯%石太平%馬大龍
류우명%팽지%산유유%석태평%마대룡
细胞水平筛选%TMEM9B%核因子κB(NF-κB)%细胞凋亡
細胞水平篩選%TMEM9B%覈因子κB(NF-κB)%細胞凋亡
세포수평사선%TMEM9B%핵인자κB(NF-κB)%세포조망
cell-based screening%TMEM9B%NF-κB%cell apoptosis
核因子κB(NF-κB)是细胞内重要的转录因子,其介导的细胞信号转导通路在细胞凋亡中的作用是国内外研究的热点.为了筛选NF-κB通路相关新基因,建立了基于细胞水平的报告基因高通量筛选模型.利用双荧光素酶报告系统检测报告基因荧光索酶活性,通过对构建的439个人类未知功能基因的筛选,获得了一批激活NF-κB信号通路的功能基因,其中基因TMEM9B可以明显激活NF-κB通路.进一步实验显示TME9B激活NF-κB通路呈明显剂量依赖性,Western blot及EMSA实验证实,TMEM9B能够促进胞质内NF-κB的抑制分子IκBα的降解,并促使NF-κB由胞质向胞核转移,同时流式细胞术实验发现TMEM9B可引起293T和HeLa细胞的凋亡.总之,所建立的基于细胞水平的NF-κB通路筛选模型稳定高效,筛选并验证TMEM9B可明显激活NF-κB信号转导通路,并从而引起细胞凋亡.
覈因子κB(NF-κB)是細胞內重要的轉錄因子,其介導的細胞信號轉導通路在細胞凋亡中的作用是國內外研究的熱點.為瞭篩選NF-κB通路相關新基因,建立瞭基于細胞水平的報告基因高通量篩選模型.利用雙熒光素酶報告繫統檢測報告基因熒光索酶活性,通過對構建的439箇人類未知功能基因的篩選,穫得瞭一批激活NF-κB信號通路的功能基因,其中基因TMEM9B可以明顯激活NF-κB通路.進一步實驗顯示TME9B激活NF-κB通路呈明顯劑量依賴性,Western blot及EMSA實驗證實,TMEM9B能夠促進胞質內NF-κB的抑製分子IκBα的降解,併促使NF-κB由胞質嚮胞覈轉移,同時流式細胞術實驗髮現TMEM9B可引起293T和HeLa細胞的凋亡.總之,所建立的基于細胞水平的NF-κB通路篩選模型穩定高效,篩選併驗證TMEM9B可明顯激活NF-κB信號轉導通路,併從而引起細胞凋亡.
핵인자κB(NF-κB)시세포내중요적전록인자,기개도적세포신호전도통로재세포조망중적작용시국내외연구적열점.위료사선NF-κB통로상관신기인,건립료기우세포수평적보고기인고통량사선모형.이용쌍형광소매보고계통검측보고기인형광색매활성,통과대구건적439개인류미지공능기인적사선,획득료일비격활NF-κB신호통로적공능기인,기중기인TMEM9B가이명현격활NF-κB통로.진일보실험현시TME9B격활NF-κB통로정명현제량의뢰성,Western blot급EMSA실험증실,TMEM9B능구촉진포질내NF-κB적억제분자IκBα적강해,병촉사NF-κB유포질향포핵전이,동시류식세포술실험발현TMEM9B가인기293T화HeLa세포적조망.총지,소건립적기우세포수평적NF-κB통로사선모형은정고효,사선병험증TMEM9B가명현격활NF-κB신호전도통로,병종이인기세포조망.
Nuclear factor κB (NF-κB) is an important cellular transcription factor. The important role of NF-κB-mediated cell signal transduction pathway in apoptosis is a hot topic at home and abroad. In order to discover new regulators in NF-κB signaling pathway, a high-throughput cell-based screening model based on dual luciferase reporters system was established, a number of genes that can activate NF-κB signal pathway were obtained by screening of 439 novel function genes. Among them, TMEM9B can obviously activate NF-κB signaling pathway. Further experiments showed that TMEM9B activated NF-κB signaling pathway in a dose-dependent pattern. Western blotting and EMSA experiments confirmed that TMEM9B can promote the degradation of IκBα (a cytoplasm inhibitor of NF-κB), and cause NF-κB shift from the cytoplasm to nucleus. At the same time, flow cytometry result demonstrated TMEM9B can induce apoptosis in HEK293T and HeLa cells. In short, a stable and effective screening system for NF-κB has been established, through which TMEM9B was identified to be able to significantly activate NF-κB signal transduction pathway and thus cause cells apoptosis.