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核黄素转运蛋白2的人类直系同源物的功能特性及其大鼠直系同源物在小肠中的核黄素反应性表达表明其参与核黄素吸收。

Functional characteristics of the human ortholog of riboflavin transporter 2 and riboflavin-responsive expression of its rat ortholog in the small intestine indicate its involvement in riboflavin absorption.

作者信息

Fujimura Misaki, Yamamoto Syunsuke, Murata Tomoaki, Yasujima Tomoya, Inoue Katsuhisa, Ohta Kin-ya, Yuasa Hiroaki

机构信息

Department of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan.

出版信息

J Nutr. 2010 Oct;140(10):1722-7. doi: 10.3945/jn.110.128330. Epub 2010 Aug 19.

Abstract

Riboflavin transporter (RFT) 2 has recently been identified as a transporter that may be, mainly based on the functional characteristics of its rat ortholog (rRFT2), involved in the intestinal absorption of riboflavin. The present study was conducted to further examine such a possible role of RFT2, focusing on the functional characteristics of its human ortholog (hRFT2) and the response of rRFT2 expression in the small intestine to deprivation of dietary riboflavin. When transiently expressed in human embryonic kidney 293 cells, hRFT2 could transport riboflavin efficiently in a pH-sensitive manner, favoring acidic pH and without requiring Na(+). Riboflavin transport by hRFT2 was saturable with a Michaelis constant of 0.77 μmol/L at pH 6.0, and inhibited by some riboflavin derivatives, such as lumiflavin. It was also inhibited, to a lesser extent, by some cationic compounds, such as ethidium. Thus, hRFT2 was suggested to, together with a finding that its mRNA is highly expressed in the small intestine, have characteristics as an intestinal RFT. Furthermore, feeding rats a riboflavin-deficient diet caused an upregulation of the expression of rRFT2 mRNA in the small intestine, presumably as an adaptive response to enhance riboflavin absorption, which would involve rRFT2, and its apically localized characteristic was suggested by the observation of rRFT2 tagged with green fluorescent protein stably expressed in polarized Madin-Darby canine kidney II cells. All these results combined indicate that RFT2 is a transporter involved in the epithelial uptake of riboflavin in the small intestine for its nutritional utilization.

摘要

最近,核黄素转运蛋白(RFT)2被确定为一种转运蛋白,主要基于其大鼠同源物(rRFT2)的功能特性,它可能参与核黄素的肠道吸收。本研究旨在进一步探讨RFT2的这种可能作用,重点关注其人类同源物(hRFT2)的功能特性以及小肠中rRFT2表达对膳食核黄素缺乏的反应。当在人胚肾293细胞中瞬时表达时,hRFT2能够以pH敏感的方式高效转运核黄素,偏好酸性pH且不需要Na(+)。hRFT2介导的核黄素转运具有饱和性,在pH 6.0时米氏常数为0.77 μmol/L,并受到一些核黄素衍生物(如黄素)的抑制。它也受到一些阳离子化合物(如溴化乙锭)的较小程度抑制。因此,鉴于hRFT2的mRNA在小肠中高度表达这一发现,提示hRFT2具有肠道RFT的特征。此外,给大鼠喂食核黄素缺乏饮食会导致小肠中rRFT2 mRNA表达上调,推测这是一种增强核黄素吸收的适应性反应,其中涉及rRFT2,并且在极化的Madin-Darby犬肾II细胞中稳定表达的绿色荧光蛋白标记的rRFT2的观察结果提示了其顶端定位特征。所有这些结果综合表明,RFT2是一种参与小肠上皮摄取核黄素以供营养利用的转运蛋白。

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