Miyamoto K, Tatsumi S, Morimoto A, Minami H, Yamamoto H, Sone K, Taketani Y, Nakabou Y, Oka T, Takeda E
Department of Nutrition, School of Medicine, University of Tokushima, Japan.
Biochem J. 1994 Nov 1;303 ( Pt 3)(Pt 3):877-83. doi: 10.1042/bj3030877.
Recent studies suggest that the jejunal/kidney-type facilitative glucose transporter (GLUT5) functions as a high-affinity D-fructose transporter. However, its precise role in the small intestine is not clear. In an attempt to identify the fructose transporter in the small intestine, we measured fructose uptake in Xenopus oocytes expressing jejunal mRNA from five species (rat, mouse, rabbit, hamster and guinea-pig). Only jejunal mRNA from the rabbit significantly increased fructose uptake. We also cloned a rabbit GLUT5 cDNA from a jejunal library The predicted amino acid sequence of the 487-residue rabbit GLUT5 showed 72.3 and 67.1% identity with human and rat GLUT5 respectively. Northern-blot analysis revealed GLUT5 transcripts in rabbit duodenum, jejunum and, to a lesser extent, kidney. After separation of rabbit jejunal mRNA on a sucrose density gradient, the fractions that conferred D-fructose transport activity in oocytes also hybridized with rabbit GLUT5 cDNA. Hybrid depletion of jejunal mRNA with a GLUT5 antisense oligonucleotide markedly inhibited the mRNA-induced fructose uptake in oocytes. Immunoblot analysis indicated that GLUT5 (49 kDa) is located in the brush-border membrane of rabbit intestinal epithelial cells. Xenopus oocytes injected with rabbit GLUT5 cRNA exhibited fructose uptake activity with a Km of 11 mM for D-fructose. D-Fructose transport by GLUT5 was significantly inhibited by D-glucose and D-galactose. D-Fructose uptake in brush-border membrane vesicles shows a Km similar to that of GLUT5, but was not inhibited by D-glucose or D-galactose. Finally, cytochalasin B photolabelled a 49 kDa protein in rabbit brush-border-membrane preparations that was immunoprecipitated by antibodies to GLUT5. Our results suggest that GLUT5 functions as a fructose transporter in rabbit small intestine. However, biochemical properties of fructose transport in Xenopus oocytes injected with GLUT5 cRNA differed from those in rabbit jejunal vesicles.
近期研究表明,空肠/肾型易化葡萄糖转运体(GLUT5)作为一种高亲和力的D-果糖转运体发挥作用。然而,其在小肠中的精确作用尚不清楚。为了鉴定小肠中的果糖转运体,我们检测了表达来自五个物种(大鼠、小鼠、兔子、仓鼠和豚鼠)空肠mRNA的非洲爪蟾卵母细胞对果糖的摄取情况。只有来自兔子的空肠mRNA显著增加了果糖摄取。我们还从空肠文库中克隆了兔GLUT5 cDNA。预测的由487个氨基酸残基组成的兔GLUT5的氨基酸序列与人类和大鼠GLUT5的同一性分别为72.3%和67.1%。Northern印迹分析显示兔十二指肠、空肠以及程度较轻的肾脏中有GLUT5转录本。在蔗糖密度梯度上分离兔空肠mRNA后,赋予卵母细胞D-果糖转运活性的组分也与兔GLUT5 cDNA杂交。用GLUT5反义寡核苷酸对空肠mRNA进行杂交去除,显著抑制了mRNA诱导的卵母细胞对果糖的摄取。免疫印迹分析表明,GLUT5(49 kDa)位于兔肠上皮细胞的刷状缘膜中。注射了兔GLUT5 cRNA的非洲爪蟾卵母细胞表现出果糖摄取活性,对D-果糖的Km值为11 mM。GLUT5介导的D-果糖转运受到D-葡萄糖和D-半乳糖的显著抑制。刷状缘膜囊泡中D-果糖的摄取显示出与GLUT5相似的Km值,但不受D-葡萄糖或D-半乳糖的抑制。最后,细胞松弛素B对兔刷状缘膜制剂中的一种49 kDa蛋白质进行光标记,该蛋白质可被抗GLUT5抗体免疫沉淀。我们的结果表明,GLUT5在兔小肠中作为果糖转运体发挥作用。然而,注射了GLUT5 cRNA的非洲爪蟾卵母细胞中果糖转运的生化特性与兔空肠囊泡中的不同。