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首页> 外文期刊>The Journal of Nutritional Biochemistry >Identification of regulatory mechanisms of intestinal folate transport in condition of folate deficiency
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Identification of regulatory mechanisms of intestinal folate transport in condition of folate deficiency

机译:叶酸缺乏时肠道叶酸运输调控机制的确定

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摘要

Folic acid is an essential micronutrient, deficiency of which can lead to disturbance in various metabolic processes of cell. Folate transport across intestine occurs via the involvement of specialized folate transporters viz, proton coupled folate transporter (PCFT) and reduced folate carrier (RFC), which express at the membrane surfaces. The current study was designed to identify the regulatory mechanisms underlying the effects of folate deficiency (FD) on folate transport in human intestinal cell line as well as in rats and to check the reversibility of such effects. Caco-2 cells were grown for five generations in control and FD medium. Following treatment, one subgroup of cells was shifted on folate sufficient medium and grown for three more generations. Similarly, rats were fed an FD diet for 3 and 5 months, and after 3 months of FD treatment, one group of rats were shifted on normal folate-containing diet. Increase in folate transport and expression of folate transporters were observed on FD treatment. However, when cells and rats were shifted to control conditions after treatment, transport and expression of these genes restored to the control level. FD was found to have no impact on promoter methylation of PCFT and RFC; however, messenger RNA stability of transporters was found to be decreased, suggesting some adaptive response. Overall, increased expression of transporters under FD conditions can be attributed to enhanced rate of transcription of folate transporters and also to the increased binding of specificity protein 1 transcription factor to the RFC promoter only. (C) 2015 Elsevier Inc. All rights reserved.
机译:叶酸是必需的微量营养素,其缺乏会导致细胞各种代谢过程的紊乱。通过专门的叶酸转运蛋白,即质子偶联的叶酸转运蛋白(PCFT)和还原的叶酸载体(RFC)的参与,可以在整个肠道内进行叶酸转运,它们在膜表面表达。当前的研究旨在确定潜在的叶酸缺乏(FD)对人肠道细胞和大鼠中叶酸转运的调节机制,并检查这种作用的可逆性。 Caco-2细胞在对照和FD培养基中生长五代。处理后,将一个亚组细胞转移到叶酸充足的培养基上,再生长三代。类似地,给大鼠喂食FD饮食3个月和5个月,在FD治疗3个月后,将一组大鼠转入含叶酸的正常饮食。在FD治疗中观察到叶酸转运和叶酸转运蛋白表达的增加。然而,当细胞和大鼠在治疗后转移至对照条件时,这些基因的转运和表达恢复至对照水平。发现FD对PCFT和RFC的启动子甲基化没有影响。然而,发现转运蛋白的信使RNA的稳定性降低了,表明有一定的适应性反应。总体而言,FD条件下转运蛋白表达的增加可归因于叶酸转运蛋白转录速度的提高,也可归因于特异性蛋白1转录因子仅与RFC启动子结合的增加。 (C)2015 Elsevier Inc.保留所有权利。

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