Author
Listed:
- John C. Clapham
(Departments of Vascular Biology)
- Jonathan R. S. Arch
(Departments of Vascular Biology)
- Helen Chapman
(Departments of Vascular Biology)
- Andrea Haynes
(Departments of Vascular Biology)
- Carolyn Lister
(Departments of Vascular Biology)
- Gary B. T. Moore
(Departments of Vascular Biology)
- Valerie Piercy
(Departments of Vascular Biology)
- Sabrina A. Carter
(Departments of Vascular Biology)
- Ines Lehner
(Departments of Vascular Biology)
- Stephen A. Smith
(Departments of Vascular Biology)
- Lee J. Beeley
(Bioinformatics
Pfizer Ltd)
- Robert J. Godden
(Molecular Biology)
- Nicole Herrity
(Gene Expression Sciences)
- Mark Skehel
(Bioanalytical Sciences)
- K. Kumar Changani
(Departments of Safety Assessment)
- Paul D. Hockings
(Departments of Safety Assessment)
- David G. Reid
(Departments of Safety Assessment)
- Sarah M. Squires
(Departments of Safety Assessment)
- Jonathan Hatcher
(Neurobehavioiural Research)
- Brenda Trail
(Neurobehavioiural Research)
- Judy Latcham
(Laboratory Animal Sciences)
- Sohaila Rastan
(SmithKline Beecham Pharmaceuticals)
- Alexander J. Harper
(Neurobehavioiural Research)
- Susana Cadenas
(University of Cambridge
MRC-Dunn Human Nutrition Unit)
- Julie A. Buckingham
(University of Cambridge
MRC-Dunn Human Nutrition Unit)
- Martin D. Brand
(University of Cambridge
MRC-Dunn Human Nutrition Unit)
- Alejandro Abuin
(SmithKline Beecham Pharmaceuticals
Lexicon Genetics)
Abstract
Uncoupling protein-3 (UCP-3) is a recently identified member of the mitochondrial transporter superfamily1,2 that is expressed predominantly in skeletal muscle1,2. However, its close relative UCP-1 is expressed exclusively in brown adipose tissue, a tissue whose main function is fat combustion and thermogenesis. Studies on the expression of UCP-3 in animals and humans in different physiological situations support a role for UCP-3 in energy balance and lipid metabolism3,4. However, direct evidence for these roles is lacking. Here we describe the creation of transgenic mice that overexpress human UCP-3 in skeletal muscle. These mice are hyperphagic but weigh less than their wild-type littermates. Magnetic resonance imaging shows a striking reduction in adipose tissue mass. The mice also exhibit lower fasting plasma glucose and insulin levels and an increased glucose clearance rate. This provides evidence that skeletal muscle UCP-3 has the potential to influence metabolic rate and glucose homeostasis in the whole animal.
Suggested Citation
John C. Clapham & Jonathan R. S. Arch & Helen Chapman & Andrea Haynes & Carolyn Lister & Gary B. T. Moore & Valerie Piercy & Sabrina A. Carter & Ines Lehner & Stephen A. Smith & Lee J. Beeley & Robert, 2000.
"Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean,"
Nature, Nature, vol. 406(6794), pages 415-418, July.
Handle:
RePEc:nat:nature:v:406:y:2000:i:6794:d:10.1038_35019082
DOI: 10.1038/35019082
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