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Isolation and Differentiation of Stromal Vascular Cells to Beige/Brite Cells
Published on: March 28, 2013
Wnt10b inhibits development of white and brown adipose tissues
Kenneth A Longo1, Wendy S Wright, Sona Kang
1Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Abstract:
Wnt is a family of secreted signaling proteins that regulate diverse developmental processes. Activation of canonical Wnt signaling by Wnt10b inhibits differentiation of preadipocytes in vitro. To determine whether Wnt signaling blocks adipogenesis in vivo, we created transgenic mice in which Wnt10b is expressed from the FABP4 promoter. Expression of Wnt10b in adipose impairs development of this tissue throughout the body, with a decline of approximately 50% in total body fat and a reduction of approximately 60% in weight of epididymal and perirenal depots. FABP4-Wnt10b mice resist accumulation of adipose tissue when fed a high fat diet. Furthermore, transgenic mice are more glucose-tolerant and insulin-sensitive than wild type mice. Expression of Wnt10b from the FABP4 promoter also blocks development of brown adipose tissue. Interscapular tissue of FABP4-Wnt10b mice has the visual appearance of white adipose tissue but expresses neither brown (e.g. uncoupling protein 1) nor white adipocyte markers. Transgenic mice are unable to maintain a core body temperature when placed in a cold environment, providing further evidence that Wnt10b inhibits development of brown adipose tissue. Although food intake is not altered in FABP4-Wnt10b mice, oxygen consumption is decreased. Thus, FABP4-Wnt10b mice on a chow diet gain more weight than controls, largely because of an increase in weight of skin. In summary, inhibition by Wnt10b of white and brown adipose tissue development results in lean mice without lipodystrophic diabetes.
Insights
Wnt10b protein expression in adipose tissue blocks the development of both white and brown fat in mice. This results in leaner animals with improved glucose tolerance and insulin sensitivity, even on a high-fat diet.
Area of Science:
- Cell Biology
- Developmental Biology
- Metabolic Research
Background:
- Wnt signaling proteins regulate crucial developmental processes.
- Wnt10b activation of canonical Wnt signaling inhibits preadipocyte differentiation in vitro.
Purpose of the Study:
- To investigate if Wnt signaling blocks adipogenesis in vivo.
- To determine the effects of Wnt10b expression in adipose tissue on overall metabolism and fat development.
Main Methods:
- Created transgenic mice (FABP4-Wnt10b) expressing Wnt10b under the FABP4 promoter.
- Assessed body fat, tissue weights, response to high-fat diet, glucose tolerance, insulin sensitivity, and cold tolerance.
Main Results:
- FABP4-Wnt10b mice showed a ~50% decrease in total body fat and ~60% reduction in specific fat depots.
- Transgenic mice resisted high-fat diet-induced adiposity, exhibited improved glucose tolerance and insulin sensitivity.
- Development of both white and brown adipose tissue was inhibited, impacting thermoregulation and oxygen consumption.
Conclusions:
- Wnt10b expression in adipose tissue effectively inhibits both white and brown adipogenesis in vivo.
- FABP4-driven Wnt10b expression leads to lean mice with metabolic benefits, offering insights into fat development regulation.
- This study highlights Wnt10b as a key regulator of adipose tissue development and metabolic homeostasis.
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