Literature DB >> 26905426

Trehalose inhibits solute carrier 2A (SLC2A) proteins to induce autophagy and prevent hepatic steatosis.

Brian J DeBosch1, Monique R Heitmeier2, Allyson L Mayer2, Cassandra B Higgins2, Jan R Crowley3, Thomas E Kraft2, Maggie Chi4, Elizabeth P Newberry3, Zhouji Chen3, Brian N Finck3, Nicholas O Davidson3, Kevin E Yarasheski3, Paul W Hruz2, Kelle H Moley4.   

Abstract

Trehalose is a naturally occurring disaccharide that has gained attention for its ability to induce cellular autophagy and mitigate diseases related to pathological protein aggregation. Despite decades of ubiquitous use as a nutraceutical, preservative, and humectant, its mechanism of action remains elusive. We showed that trehalose inhibited members of the SLC2A (also known as GLUT) family of glucose transporters. Trehalose-mediated inhibition of glucose transport induced AMPK (adenosine 5'-monophosphate-activated protein kinase)-dependent autophagy and regression of hepatic steatosis in vivo and a reduction in the accumulation of lipid droplets in primary murine hepatocyte cultures. Our data indicated that trehalose triggers beneficial cellular autophagy by inhibiting glucose transport.
Copyright © 2016, American Association for the Advancement of Science.

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Year:  2016        PMID: 26905426      PMCID: PMC4816640          DOI: 10.1126/scisignal.aac5472

Source DB:  PubMed          Journal:  Sci Signal        ISSN: 1945-0877            Impact factor:   8.192


  36 in total

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  95 in total

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