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- W2127014382 abstract "Upon binding and activating its cell-surface receptor, insulin triggers signaling cascades that regulate many cellular processes. Regarding glucose homeostasis, insulin suppresses hepatic glucose production and increases glucose transport into muscle and adipose tissues. At the cellular level, glucose uptake results from the insulin-stimulated translocation of the glucose transporter 4 (GLUT4) from intracellular storage sites to the plasma membrane. Although the signaling molecules that function proximal to the activated insulin receptor have been well characterized, it is not known how the distal insulin-signaling cascade interfaces with and mobilizes GLUT4-containing compartments. Recently, several candidate signaling molecules, including AS160, PIKfyve and synip, have been identified that might provide functional links between the insulin signaling cascade and GLUT4 compartments. Future work will focus on delineating the precise GLUT4 trafficking steps regulated by these molecules." @default.
- W2127014382 created "2016-06-24" @default.
- W2127014382 creator A5077728712 @default.
- W2127014382 creator A5091087458 @default.
- W2127014382 date "2006-04-01" @default.
- W2127014382 modified "2023-10-15" @default.
- W2127014382 title "Bridging the GAP between insulin signaling and GLUT4 translocation" @default.
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- W2127014382 doi "https://doi.org/10.1016/j.tibs.2006.02.007" @default.
- W2127014382 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16540333" @default.
- W2127014382 hasPublicationYear "2006" @default.
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