幽門螺桿菌CagA通過(guò)B-Raf和JNK2調(diào)節(jié)原癌蛋白CIP2A表達(dá)及其細(xì)胞生物學(xué)作用研究
發(fā)布時(shí)間:2018-08-17 08:33
【摘要】:目的了解幽門螺桿菌CagA上調(diào)CIP2A表達(dá)的分子機(jī)制。方法培養(yǎng)AGS細(xì)胞和GES-1細(xì)胞,一部分細(xì)胞分別轉(zhuǎn)染CagA陽(yáng)性質(zhì)粒WT-cagA和陰性對(duì)照質(zhì)粒pcDNA3.1;另一部分細(xì)胞用B-Raf和JNK2信號(hào)抑制劑作用,然后分別轉(zhuǎn)染質(zhì)粒WT-cagA和質(zhì)粒pcDNA3.1,Western blot檢測(cè)CIP2A表達(dá),細(xì)胞克隆形成試驗(yàn)檢測(cè)細(xì)胞增殖能力,細(xì)胞遷移試驗(yàn)檢測(cè)細(xì)胞遷移能力結(jié)果 AGS細(xì)胞和GES-1細(xì)胞轉(zhuǎn)染CagA陽(yáng)性質(zhì)粒WT-cagA后CIP2A表達(dá)量增多;細(xì)胞經(jīng)B-Raf和JNK2的信號(hào)抑制劑作用后轉(zhuǎn)染CagA陽(yáng)性質(zhì)粒WT-cagA,其CIP2A表達(dá)量比僅轉(zhuǎn)染質(zhì)粒WT-cagA的細(xì)胞表達(dá)量少,細(xì)胞的克隆數(shù)減少,細(xì)胞遷移能力降低。結(jié)論幽門螺桿菌CagA進(jìn)入細(xì)胞通過(guò)B-Raf和JNK2及其參與的信號(hào)途徑調(diào)節(jié)原癌蛋白CIP2A的表達(dá),進(jìn)而影響細(xì)胞的克隆形成能力和遷移能力。
[Abstract]:Objective to investigate the molecular mechanism of CagA upregulation of CIP2A expression in Helicobacter pylori. Methods AGS cells and GES-1 cells were cultured, some of them were transfected with CagA positive plasmid WT-cagA and the other were transfected with B-Raf and JNK2 signal inhibitors, and then transfected with WT-cagA and pcDNA3.1 Western blot to detect the expression of CIP2A. The ability of cell proliferation was detected by cell clone formation assay, and the expression of CIP2A was increased after transfection of CagA positive plasmid WT-cagA into AGS cells and GES-1 cells by cell migration assay. After transfection of WT-cagA into CagA positive plasmid WT-cagA by signal inhibitor of B-Raf and JNK2, the expression of CIP2A was less than that of only transfected plasmid WT-cagA, the number of cell clones was decreased, and the ability of cell migration was decreased. Conclusion Helicobacter pylori CagA enters the cells and regulates the expression of proto-oncoprotein CIP2A through B-Raf, JNK2 and its signal pathway, which affects the ability of cell clone formation and migration.
【作者單位】: 鄭州大學(xué)第一附屬醫(yī)院麻醉科;泰山醫(yī)學(xué)院病原生物學(xué)教研室;泰山醫(yī)學(xué)院附屬醫(yī)院檢驗(yàn)科;泰山醫(yī)學(xué)院公共衛(wèi)生學(xué)院;山東省泰山療養(yǎng)院內(nèi)科;泰山醫(yī)學(xué)院第二臨床醫(yī)學(xué)院;
【基金】:國(guó)家自然科學(xué)基金項(xiàng)目(No.81602455) 山東省自然科學(xué)基金項(xiàng)目(No.ZR2013HM033,ZR2013HL057,ZR2013HL060) 泰山醫(yī)學(xué)院重大科研專項(xiàng)(No.2014GCC10) 泰安市科研課題(No.2015NS2098,2016NS1074,2016NS1089)
【分類號(hào)】:R735.2
本文編號(hào):2187060
[Abstract]:Objective to investigate the molecular mechanism of CagA upregulation of CIP2A expression in Helicobacter pylori. Methods AGS cells and GES-1 cells were cultured, some of them were transfected with CagA positive plasmid WT-cagA and the other were transfected with B-Raf and JNK2 signal inhibitors, and then transfected with WT-cagA and pcDNA3.1 Western blot to detect the expression of CIP2A. The ability of cell proliferation was detected by cell clone formation assay, and the expression of CIP2A was increased after transfection of CagA positive plasmid WT-cagA into AGS cells and GES-1 cells by cell migration assay. After transfection of WT-cagA into CagA positive plasmid WT-cagA by signal inhibitor of B-Raf and JNK2, the expression of CIP2A was less than that of only transfected plasmid WT-cagA, the number of cell clones was decreased, and the ability of cell migration was decreased. Conclusion Helicobacter pylori CagA enters the cells and regulates the expression of proto-oncoprotein CIP2A through B-Raf, JNK2 and its signal pathway, which affects the ability of cell clone formation and migration.
【作者單位】: 鄭州大學(xué)第一附屬醫(yī)院麻醉科;泰山醫(yī)學(xué)院病原生物學(xué)教研室;泰山醫(yī)學(xué)院附屬醫(yī)院檢驗(yàn)科;泰山醫(yī)學(xué)院公共衛(wèi)生學(xué)院;山東省泰山療養(yǎng)院內(nèi)科;泰山醫(yī)學(xué)院第二臨床醫(yī)學(xué)院;
【基金】:國(guó)家自然科學(xué)基金項(xiàng)目(No.81602455) 山東省自然科學(xué)基金項(xiàng)目(No.ZR2013HM033,ZR2013HL057,ZR2013HL060) 泰山醫(yī)學(xué)院重大科研專項(xiàng)(No.2014GCC10) 泰安市科研課題(No.2015NS2098,2016NS1074,2016NS1089)
【分類號(hào)】:R735.2
【相似文獻(xiàn)】
相關(guān)期刊論文 前2條
1 王石松;;CIP2A在慢性粒細(xì)胞白血病中的表達(dá)及意義[J];中國(guó)醫(yī)學(xué)創(chuàng)新;2013年09期
2 吳丹丹;王彩花;;CagA與胃MALT淋巴瘤的相關(guān)性及發(fā)病機(jī)制的研究進(jìn)展[J];國(guó)際消化病雜志;2008年03期
相關(guān)博士學(xué)位論文 前1條
1 趙磊;維生素B12代謝基因多態(tài)與胃癌的相關(guān)性研究[D];蘭州大學(xué);2017年
相關(guān)碩士學(xué)位論文 前4條
1 張莉羚;lncRNA AC006050.3在胃癌組織中上調(diào)的表達(dá)及臨床病理分析[D];蘭州大學(xué);2017年
2 林傳真;中性粒細(xì)胞與淋巴細(xì)胞的比值與胃癌患者預(yù)后的關(guān)系[D];福建醫(yī)科大學(xué);2017年
3 趙丹蕊;EB病毒相關(guān)胃癌中RASSF1A基因甲基化狀態(tài)和表達(dá)的研究[D];青島大學(xué);2017年
4 郭魯偉;FGGY在胃癌中作用的初步探討[D];鄭州大學(xué);2017年
,本文編號(hào):2187060
本文鏈接:http://sikaile.net/yixuelunwen/zlx/2187060.html
最近更新
教材專著