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Functional characterisation of human SGLT-5 as a novel kidney-specific sodium-dependent sugar transporter

  作者 Grempler, R; Augustin, R; Froehner, S; Hildebrandt, T; Simon, E; Mark, M; Eickelmann, P  
  选自 期刊  FEBS Letters;  卷期  2012年586-3;  页码  248-253  
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[摘要]Sodium glucose cotransporters (SGLT) actively catalyse carbohydrate transport across cellular membranes. Six of the 12 known SGLT family members have the capacity to bind and/or transport monosaccharides (SGLT-1 to 6); of these, all but SGLT-5 have been characterised. Here we demonstrate that human SGLT-5 is exclusively expressed in the kidney. Four splice variants were detected and the most abundant SGLT-5-mRNA was functionally characterised. SGLT-5 mediates sodium-dependent [C-14]-alpha-methyl-D-glucose (AMG) transport that can be inhibited by mannose, fructose, glucose, and galactose. Uptake studies using demonstrated high capacity transport for mannose and fructose and, to a lesser extent, glucose, AMG, and galactose. SGLT-5 mediated mannose, fructose and AMG transport was weakly (mu M potency) inhibited by SGLT-2 inhibitors. In summary, we have characterised SGLT-5 as a kidney mannose transporter. Further studies are warranted to explore the physiological role of SGLT-5. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

 
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