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991.
992.
Lan Yang Yiming Ma Wenxiao Han Weiwei Li Liang Cui Xinhua Zhao Yantao Tian Zhixiang Zhou Wengong Wang Hongying Wang 《The Journal of biological chemistry》2015,290(44):26627-26637
Proteinase activated-receptor 2 (PAR2) participates in cancer metastasis promoted by serine proteinases. The current study aimed to test the molecular mechanism by which PAR2 promotes cancer cell migration. In different cancer cells, activation of PAR2 by activating peptide (PAR2-AP) dramatically increased cell migration, whereas knock down of PAR2 inhibited cellular motility. The PAR2 activation also repressed miR-125b expression while miR-125b mimic successfully blocked PAR2-induced cell migration. Moreover, Grb associated-binding protein 2 (Gab2) was identified as a novel target gene of miR-125b and it mediated PAR2-induced cell migration. The correlation of PAR2 with miR-125b and Gab2 was further supported by the findings obtained from human colorectal carcinoma specimens. Remarkably, knock down of NOP2/Sun domain family, member 2 (NSun2), a RNA methyltransferase, blocked the reduction in miR-125b induced by PAR2. Furthermore, PAR2 activation increased the level of N6-methyladenosine (m6A)-containing pre-miR-125b in NSun2-dependent manner. Taken together, our results demonstrated that miR-125b mediates PAR2-induced cancer cell migration by targeting Gab2 and that NSun2-dependent RNA methylation contributes to the down-regulation of miR-125b by PAR2 signaling. These findings suggest a novel epigenetic mechanism by which microenvironment regulates cancer cell migration by altering miRNA expression. 相似文献
993.
Supercapacitors: A Layered‐Nanospace‐Confinement Strategy for the Synthesis of Two‐Dimensional Porous Carbon Nanosheets for High‐Rate Performance Supercapacitors (Adv. Energy Mater. 7/2015) 下载免费PDF全文
994.
Lithium Batteries: Highly Nitridated Graphene–Li2S Cathodes with Stable Modulated Cycles (Adv. Energy Mater. 23/2015) 下载免费PDF全文
995.
Li‐Fei Bai Hua Zhao Cheng‐Yi Tang Yan‐Jun Pang Rong‐Wu Yang Xiao‐Ming Wang Gui‐Hua Lu Yong‐Hua Yang 《Chirality》2015,27(3):274-280
In this study, a shikonin ester derivative, compound 3g , was selected to evaluate its anticancer activities and we found that compound 3g exhibited better antitubulin activities against the human HepG2 cell line with an IC50 value of 1.097 μM. Furthermore, the inhibition of tubulin polymerization results indicated that compound 3g demonstrated the most potent antitubulin activity (IC50 = 13.88), which was compared with shikonin and colchicine as positive controls (IC50 = 25.28 μM and 22.56 μM), respectively. Compound 3g was simulated to have good binding site with tubulin and arrested the cell cycle at G2/M phase, which also induces apoptosis in HepG2 cells, in which P53 and members of Bcl‐2 protein family were both involved in the progress of apoptosis revealed by western blot. Confocal microscopy observations revealed compound 3g targeted tubulin and altered its polymerization by interfering with microtubule organization. Based on these results, compound 3g functions as a potent anticancer agent targeting tubulin. Chirality 27:274–280, 2015.. © 2015 Wiley Periodicals, Inc. 相似文献
996.
997.
998.
气候假说对内蒙古草原群落物种多样性格局的解释 总被引:1,自引:0,他引:1
物种丰富度的地理格局是宏观生态学和生物地理学的中心议题之一。本文基于内蒙古草原192个野外样地的调查数据, 结合各样地年平均气温、年降水量等9个气候因子, 探讨内蒙古草原物种丰富度格局及其主导因素, 以确定气候假说在该区的适用性。结果表明: (1)内蒙古草原物种丰富度经度格局显著, 呈现沿经度升高而增加的趋势, 同时由于经纬度的共线性, 也呈现出沿纬度升高而增加的趋势。(2)方差分解显示, 能量单独解释率为2.7%, 水分单独解释率为11.4%, 水分和能量共同解释率为46.3%, 未解释部分为39.6%, 可见能量与水分的共同作用在物种丰富度格局形成中占主导地位, 支持水热动态假说。这说明水热动态假说适用于解释内蒙古草原物种丰富度 格局。 相似文献
999.
Fibroblast growth factor (FGF) has been known to regulate the proliferation and differentiation of a variety of cell types via interaction with a specific FGF receptor on the cell surface. In the present study, Fgf8 cDNA of Mexican axolotl, Ambystoma mexicanum, was expressed in Escherichia coli as an MBP-FGF8 fusion protein. The cell proliferation activity of the recombinant FGF8 (rFGF8) was measured by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazoliumbromide (MTT) assay. The addition of rFGF8 to the culture medium enhanced proliferation of BALB/c 3T3 and BHK21 cells about 1.4--1.5 fold. To analyze the binding activity of rFGF8 to the cell surface, cell surface enzyme linked immunosorbent assay was developed. Comparison of the structure of basic FGF with the computer-simulated structure of FGF8 suggested that Tyr-58, Glu-132, Tyr-139, and Leu-179 might be the potential receptor binding sites. Amino acid substitution muteins of FGF8 were constructed by PCR-derived directed mutagenesis and the muteins were overexpressed in E. coli. The rFGF8 muteins were purified and their binding activities were analyzed. Substitution of Tyr-58 or Glu-132 or Leu-179 of the FGF8 with alanine reduced the binding affinity, while substitution of Tyr-139 with alanine did not alter the binding affinity. These results imply that Tyr-58, Glu-132, and Leu-179 of FGF8 might be involved in its binding to the cell surface. 相似文献
1000.
幽门螺杆菌HspA融合蛋白口服疫苗的构建 总被引:6,自引:0,他引:6
构建表达幽门螺杆菌的保护性抗原分热休克蛋白A亚单位(HspA)和霍乱毒素B亚单位(CtxB)的重组融合蛋白的生物工程菌株,以此制备幽门螺杆菌的口服疫苗。用PCR方法扩增hspA和ctxB两个目的的基因片段,将它们分别克隆至pSK(+)质粒上,然后插入含T7启动子ET-22b(+)的表达载体中,构建嗓基因的表达质量pET-hct,转化E.coliBL21(DE3),经IPTG诱导表达融合蛋白HCT。经测序,hspA-ctxB(hct)融合基因片段由726bp组成,可以编码242个氨基酸残基的多肽。经SDS-PAGE和免疫印迹分析检测发现,融合基因表达的蛋白质相对分子质量约为30kD。融合蛋白经镍离子柱纯化、复性后,和HspA共同标记同位素^125I,然后给小鼠灌胃,结果观察到HCT组小鼠血清中的^125I的放射量要明显高于HspA组(P<0.001),且吸收峰值时间明显提前。融合蛋白中的CtxB可明显促进小鼠对HspA的吸收,HCT融合蛋白可以作为预防和治疗幽门螺杆菌感染的侯选口服疫苗。 相似文献