Marín Juez, RubénCapilla Campos, EncarnaciónCarvalho-Simoes, FranciscoCamps Camprubí, MartaPlanas Vilarnau, Josep2021-03-192021-03-192014-06-18https://hdl.handle.net/2445/175394The insulin-responsive glucose transporter GLUT4 was first described in 1988 as a result of studies on the regulation of glucose metabolism by insulin [1]. Soon after the discovery of GLUT4, several groups cloned GLUT4 in the human [2], rat [3,4] and mouse [5]. Since its discovery, GLUT4 has received, together with GLUT1, more experimental attention than any other single membrane transport protein. Structurally, GLUT4 follows the predicted model for class I glucose transporters. GLUT4 has a high affinity for glucose, with a Km of approximately 5 mM [6], and also transports mannose, galactose, dehydroascorbic acid and glucosamine [7-10]. In mammals, GLUT4 is mainly expressed in cardiac and skeletal muscle, brown and white adipose tissue, and brain [6,11,12]. GLUT4 plays a pivotal role in whole body glucose homeostasis, mediating the uptake of glucose regulated by insulin [13,14]. GLUT4 is responsible for the reduction in the postprandial rise in plasma glucose levels [6]. Insulin acts by stimulating the translocation of specific GLUT4-containing vesicles from intracellular stores to the plasma membrane (PM) resulting in an immediate increase in glucose transport [6,15]. The disruption of GLUT4 expression has been extensively associated with pathologies of impaired glucose uptake and insulin resistance such as type 2 diabetes and obesity [13,16-18]...31 p.application/pdfengcc by (c) Marín Juez, Rubén et al., 2014http://creativecommons.org/licenses/by/3.0/es/GlucosaHomeòstasiPeixosGlucoseHomeostasisFishesinfo:eu-repo/semantics/bookPart281005info:eu-repo/semantics/openAccess