GLUT5
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
GLUT5 is a fructose transporter expressed on the apical border of enterocytes in the small intestine.[5] GLUT5 allows for fructose to be transported from the intestinal lumen into the enterocyte by facilitated diffusion due to fructose's high concentration in the intestinal lumen. GLUT5 is also expressed in skeletal muscle,[6] testis, kidney, fat tissue (adipocytes), and brain.[7]
Fructose malabsorption or Dietary Fructose Intolerance is a dietary disability of the small intestine, where the amount of fructose carrier in enterocytes is deficient.[8]
In humans the GLUT5 protein is encoded by the SLC2A5 gene.[9]
Regulation
Fructose uptake rate by GLUT5 is significantly reduced by diabetes mellitus, hypertension, obesity, fructose malabsorption, and inflammation. However, age-related changes in fructose intake capability are not explained by the rate of expression of GLUT5.[10][11][12] The absorption of fructose in the simultaneous presence of glucose is improved, while sorbitol is inhibitory.[13] Fructose absorption by GLUT5 can be investigated using intestinal organoids.[14][15]
Interactive pathway map
Click on genes, proteins and metabolites below to link to respective articles.[§ 1]
- The interactive pathway map can be edited at WikiPathways: "GlycolysisGluconeogenesis_WP534".
