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首页> 外文期刊>Biological trace element research >Activation of the EIF2 alpha/ATF4 and ATF6 Pathways in DU-145 Cells by Boric Acid at the Concentration Reported in Men at the US Mean Boron Intake
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Activation of the EIF2 alpha/ATF4 and ATF6 Pathways in DU-145 Cells by Boric Acid at the Concentration Reported in Men at the US Mean Boron Intake

机译:在美国的男性浓度下,硼酸在Du-145细胞中激活eif2α/ ATF4和ATF6途径的浓度为硼摄入量

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摘要

Fruits, nuts, legumes, and vegetables are rich sources of boron (B), an essential plant nutrient with chemopreventive properties. Blood boric acid (BA) levels reflect recent B intake, and men at the US mean intake have a reported non-fasting level of 10 mu M. Treatment of DU-145 prostate cancer cells with physiological concentrations of BA inhibits cell proliferation without causing apoptosis and activates eukaryotic initiation factor 2 (eIF2 alpha). EIF2 alpha induces cell differentiation and protects cells by redirecting gene expression to manage endoplasmic reticulum stress. Our objective was to determine the temporal expression of endoplasmic reticulum (ER) stress-activated genes in DU-145 prostate cells treated with 10 mu M BA. Immunoblots showed post-treatment increases in eIF2 alpha protein at 30 min and ATF4 and ATF6 proteins at 1 h and 30 min, respectively. The increase in ATF4 was accompanied by an increase in the expression of its downstream genes growth arrest and DNA damage-induced protein 34 (GADD34) and homocysteine-induced ER protein (Herp), but a decrease in GADD153/CCAAT/enhancer-binding protein homologous protein (CHOP), a pro-apoptotic gene. The increase in ATF6 was accompanied by an increase in expression of its downstream genes GRP78/BiP, calreticulin, Grp94, and EDEM. BA did not activate IRE1 or induce cleavage of XBP1 mRNA, a target of IRE1. Low boron status has been associated with increased cancer risk, low bone mineralization, and retinal degeneration. ATF4 and BiP/GRP78 function in osteogenesis and bone remodeling, calreticulin is required for tumor suppressor p53 function and mineralization of teeth, and BiP/GRP78 and EDEM prevent the aggregation of misfolded opsins which leads to retinal degeneration. The identification of BA-activated genes that regulate its phenotypic effects provides a molecular underpinning for boron nutrition and biology.
机译:水果,坚果,豆类和蔬菜是硼(b)的丰富来源,该植物营养素具有化学预防性质。血硼酸(BA)水平反映了最近的B摄入,美国的男性意味着报告的非禁食水平为10亩M.治疗Du-145前列腺癌细胞,BA的生理浓度抑制细胞增殖而不会引起细胞凋亡并激活真核启动因子2(EIF2 alpha)。 EIF2α通过重定向基因表达来诱导细胞分化并保护细胞来管理内质网胁迫。我们的目的是确定用10μmba处理的DU-145前列腺细胞中内质网(ER)应激活化基因的时间表达。免疫印迹显示出在eIF2α蛋白的后处理在30分钟和ATF4和ATF6蛋白分别在1小时和30分钟内增加。 ATF4的增加伴随着其下游基因生长骤停血和DNA损伤诱导的蛋白34(GADD34)和同型半胱氨酸诱导的ER蛋白(HERP)的表达增加,但GADD153 / CCAAT /增强子结合蛋白的降低同源蛋白(Chec),促凋亡基因。 ATF6的增加伴随着其下游基因GRP78 / BIP,Calreticulin,GRP94和EDEM表达的增加。 BA未激活IRE1或诱导XBP1 mRNA的切割,IS1的靶标。低硼状况与癌症风险,低骨矿化和视网膜变性增加有关。 ATF4和BIP / GRP78功能在骨发生和骨重塑中,肿瘤抑制剂P53功能和牙齿矿化需要钙霉素,并且BIP / GRP78和EDEM防止错误折叠的OPSIN的聚集,导致视网膜变性。鉴定调节其表型效应的BA活化基因提供了硼营养和生物学的分子支撑。

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