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Molecular and Cellular Biology, June 2006, p. 4268-4276, Vol. 26, No. 11
0270-7306/06/$08.00+0 doi:10.1128/MCB.00081-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Institute of Physiology,1 Center for Integrative Genomics,2 Department of Pharmacology and Toxicology, University of Lausanne, Lausanne, Switzerland,3 Swiss Institute for Experimental Cancer Research, Epalinges, Switzerland,4 Department of Medicine, University of Lausanne Medical School, Lausanne, Switzerland5
Received 13 January 2006/ Accepted 3 March 2006
GLUT8 is a glucose transporter isoform expressed at high levels in testis; at intermediate levels in the brain, including the hippocampus; and at lower levels in the heart and several other tissues. GLUT8 is located in an intracellular compartment and does not appear to translocate to the cell surface, except in blastocysts, where insulin has been reported to induce its surface expression. Here, we generated mice with inactivation of the glut8 gene. We showed that expression of GLUT8 was not required for normal embryonic development and that glut8/ mice had normal postnatal development, glucose homeostasis, and response to mild stress. Adult glut8/ mice showed increased proliferation of hippocampal cells but no defect in memory acquisition and retention. Absence of GLUT8 from the heart did not alter heart size and morphology but led to an increase in P-wave duration, which was not associated with abnormal Nav1.5 Na+ channel or connexin expression. Thus, absence of GLUT8 expression in the mouse caused complex but mild physiological alterations.
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