首页> 美国卫生研究院文献>Journal of Clinical Biochemistry and Nutrition >Different sucrose-isomaltase response of Caco-2 cells to glucose and maltose suggests dietary maltose sensing
【2h】

Different sucrose-isomaltase response of Caco-2 cells to glucose and maltose suggests dietary maltose sensing

机译:Caco-2细胞对葡萄糖和麦芽糖的不同蔗糖-异麦芽糖酶反应提示饮食中麦芽糖感测

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Using the small intestine enterocyte Caco-2 cell model, sucrase-isomaltase (SI, the mucosal α-glucosidase complex) expression and modification were examined relative to exposure to different mono- and disaccharide glycemic carbohydrates. Caco-2/TC7 cells were grown on porous supports to post-confluence for complete differentiation, and dietary carbohydrate molecules of glucose, sucrose (disaccharide of glucose and fructose), maltose (disaccharide of two glucoses α-1,4 linked), and isomaltose (disaccharide of two glucoses α-1,6 linked) were used to treat the cells. qRT-PCR results showed that all the carbohydrate molecules induced the expression of the SI gene, though maltose (and isomaltose) showed an incremental increase in mRNA levels over time that glucose did not. Western blot analysis of the SI protein revealed that only maltose treatment induced a higher molecular weight band (Mw ~245 kDa), also at higher expression level, suggesting post-translational processing of SI, and more importantly a sensing of maltose. Further work is warranted regarding this putative sensing response as a potential control point for starch digestion and glucose generation in the small intestine.
机译:使用小肠肠细胞Caco-2细胞模型,相对于暴露于不同的单糖和二糖血糖碳水化合物,检查了蔗糖酶-异麦芽糖酶(SI,粘膜α-葡萄糖苷酶复合物)的表达和修饰。 Caco-2 / TC7细胞在多孔支持物上生长至汇合后完全分化,饮食中的碳水化合物糖分子包括葡萄糖,蔗糖(葡萄糖和果糖的二糖),麦芽糖(两个葡萄糖α-1,4的二糖相连)和异麦芽糖(两个葡萄糖α-1,6连接的二糖)用于处理细胞。 qRT-PCR结果显示,尽管麦芽糖(和异麦芽糖)随时间推移,mRNA水平随葡萄糖的升高而增加,但所有碳水化合物分子均诱导了SI基因的表达。对SI蛋白的蛋白质印迹分析表明,只有麦芽糖处理才能诱导更高的分子量带(Mw〜245 kDa),并且在更高的表达水平上也存在,这表明SI的翻译后加工过程,更重要的是对麦芽糖的检测。关于这种假定的感测响应作为小肠中淀粉消化和葡萄糖生成的潜在控制点,还需要做进一步的工作。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号