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Improved insulin sensitivity associated with reduced mitochondrial complex IV assembly and activity


Author: Sathyaseelan S. Deepa*,†, Daniel Pulliam*,†, Shauna Hill*,†, Yun Shi*, Michael E. Walsh*,†, Adam Salmon*,¡ì, Lauren Sloane*, Ning Zhang‡, Massimo Zeviani¡¬, Carlo Viscomi¡¬, Nicolas Musi‡¡ì, Holly Van Remmen*,†¡ì,1
1. *Barshop Institute for Longevity and Aging Studies, †Department of Cellular and Structural Biology, and ‡Diabetes Division, University of Texas Health Science Center, San Antonio, Texas, USA;
2. ¡ìGeriatric Research, Education, and Clinical Center, South Texas Veterans Health Care System, San Antonio, Texas, USA;
3. ¡¬Unit of Molecular Neurogenetics, Foundation Istituto Neurologico Carlo Besta¨CIstituto Di Ricovero e Cura a Carattere Scientifico, Milan, Italy

¡¾Abstract¡¿
Mice lacking Surf1, a complex IV assembly protein, have ∼50-70% reduction in cytochrome c oxidase activity in all tissues yet a paradoxical increase in lifespan. Here we report that Surf1−/− mice have lower body (15%) and fat (20%) mass, in association with reduced lipid storage, smaller adipocytes, and elevated indicators of fatty acid oxidation in white adipose tissue (WAT) compared with control mice. The respiratory quotient in the Surf1−/− mice was significantly lower than in the control animals (0.83¨C0.93 vs. 0.90¨C0.98), consistent with enhanced fat utilization in Surf1−/− mice. Elevated fat utilization was associated with increased insulin sensitivity measured as insulin-stimulated glucose uptake, as well as an increase in insulin receptor levels (∼2-fold) and glucose transporter type 4 (GLUT4; ∼1.3-fold) levels in WAT in the Surf1−/− mice. The expression of peroxisome proliferator-activated receptor ¦Ã-coactivator 1-¦Á (PGC-1¦Á) mRNA and protein was up-regulated by 2.5- and 1.9-fold, respectively, in WAT from Surf1−/− mice, and the expression of PGC-1¦Á target genes and markers of mitochondrial biogenesis was elevated. Together, these findings point to a novel and unexpected link between reduced mitochondrial complex IV activity, enhanced insulin sensitivity, and increased mitochondrial biogenesis that may contribute to the increased longevity in the Surf1−/− mice.¡ªDeepa, S. S., Pulliam, D., Hill, S., Shi, Y., Walsh, M. E., Salmon, A., Sloane, L., Zhang, N., Zeviani, M., Viscomi, C., Musi, N., Van Remmen, H. Improved insulin sensitivity associated with reduced mitochondrial complex IV assembly and activity.

http://www.fasebj.org/content/early/2012/12/13/fj.12-221879

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