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作 者:宋早文 张裕丰 方金勇[1] 郭一孚[1] 刘越丹 徐玲玲[1] 赵铁军[1] SONG Zaowen;ZHANG Yufeng;FANG Jinyong;GUO Yifu;LIU Yuedan;XU Lingling;ZHAO Tiejun(College of Chemdstry and Life Scieces,Zhejiang Normal,University,Jinhua 321004,China)
机构地区:[1]浙江师范大学化学与生命科学学院,浙江金华321004
出 处:《浙江师范大学学报(自然科学版)》2018年第2期194-200,共7页Journal of Zhejiang Normal University:Natural Sciences
基 金:国家自然科学基金资助项目(31470262;31200128);浙江省科技厅公益技术应用研究计划项目(2015C33149);浙江省教育厅一般科研项目(Y201738673);国家级大学生创新创业训练计划(201710345011)
摘 要:成人T细胞白血病(Adult T-cell leukemia,ATL)是与人类T淋巴细胞白血病1型病毒(Human T-cell leukemia virus type 1,HTLV-1)感染密切相关的恶性淋巴细胞白血病.HTLV-1反义编码的HBZ(HTLV-1 b ZIP factor)蛋白在ATL发生过程中扮演极为重要的角色.为了寻找治疗成人T细胞白血病的方法,设计了能与HBZ蛋白形成二聚体,从而封闭HBZ蛋白功能的靶向多肽R8-HBAP.通过免疫共沉淀实验,发现R8-HBAP可以有效抑制HBZ蛋白与下游靶蛋白c-Jun的结合,报告基因实验显示,R8-HBAP能阻遏HBZ蛋白对AP-1信号通路的调控作用.MTT和流式细胞术实验发现,R8-HBAP能抑制ATL细胞的恶性增殖并促进细胞凋亡.因此,靶向多肽R8-HBAP通过阻遏HBZ蛋白的功能从而抑制白血病细胞的恶性增殖,为R8-HBAP的开发利用及成人T细胞白血病的治疗提供一定的实验依据.Adult T-cell leukemia { ATL) was a peripheral T-cell neoplasm associated with irrfection by Human T-cell leukemia vfi'us type 1 ( HTLV-1 ). The HTLV-1 bZIP fzctor ( HBZ ), which was encoded by minus strand of provirus, was thought to play a central role in the development of ATL. In order to find out the treat- ment of ATL, it was successfully designed and selected several HBZ specific inhibitory targeting peptides (R8-HBAP). In immunoprecipitation assay, R8-HBAP could specifically associated with HBZ and therefore inhibited the interaction between HBZ and c-Jun. Reporter assay showed that R8-HBAP could overcome the repression of the AP-1 signaling by HBZ. MTT assay and flow cytometry revealed that R8-HBAP suppressed the proliferation of ATL cells and induced the apoptosis of ATL cells. In summary, R8-HBAP inhibited the proliferation of ATL cells by repressing the function of HBZ protein, and it would provide experimental basis for the further application of R8-HBAP and the treatment of adult T-cell leukemia.
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