首页> 美国卫生研究院文献>Springer Open Choice >Activation of the EIF2α/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 EIF2α/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:硼酸在美国平均硼摄入量中男性报告的浓度下激活DU-145细胞中EIF2α/ ATF4和ATF6途径的活化

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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 μM. Treatment of DU-145 prostate cancer cells with physiological concentrations of BA inhibits cell proliferation without causing apoptosis and activates eukaryotic initiation factor 2 (eIF2α). EIF2α 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 μM BA. Immunoblots showed post-treatment increases in eIF2α 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.Electronic supplementary materialThe online version of this article (doi:10.1007/s12011-016-0824-y) contains supplementary material, which is available to authorized users.
机译:水果,坚果,豆类和蔬菜是硼(B)的丰富来源,硼是一种具有化学预防特性的重要植物营养素。血硼酸(BA)水平反映了近期的B摄入量,据美国平均摄入量的男性非空腹水平据报道为10μM。用生理浓度的BA处理DU-145前列腺癌细胞可抑制细胞增殖而不会引起凋亡,并激活真核起始因子2(eIF2α)。 EIF2α通过重定向基因表达以控制内质网应激来诱导细胞分化并保护细胞。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)应激激活基因的时间表达。免疫印迹显示,处理后30分钟的eIF2α蛋白和1小时和30分钟的ATF4和ATF6蛋白分别增加。 ATF4的增加伴随其下游基因生长停滞和DNA损伤诱导的蛋白34(GADD34)和高半胱氨酸诱导的ER蛋白(Herp)的表达增加,但GADD153 / CCAAT /增强子结合蛋白减少同源蛋白(CHOP),一种促凋亡基因。 ATF6的增加伴随其下游基因GRP78 / BiP,钙网蛋白,Grp94和EDEM表达的增加。 BA不会激活IRE1或诱导IRE1的靶标XBP1 mRNA裂解。硼水平低与癌症风险增加,骨矿化低和视网膜变性有关。 ATF4和BiP / GRP78在成骨和骨重塑中起作用,钙网蛋白是抑癌p53功能和牙齿矿化所必需的,而BiP / GRP78和EDEM可以防止视蛋白错误折叠的聚集,从而导致视网膜变性。鉴定调节其表型效应的BA激活基因为硼营养和生物学提供了分子基础。电子补充材料本文的在线版本(doi:10.1007 / s12011-016-0824-y)包含补充材料给授权用户。

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