The Wnt Signaling Pathway Effector TCF7L2 Controls Gut and Brain Proglucagon Gene Expression and Glucose Homeostasis
- Weijuan Shao1,2,
- Dingyan Wang1,3,
- Yu-Ting Chiang1,4,
- Wilfred Ip1,2,
- Lingyun Zhu3,4,
- Fenghao Xu1,2,
- Joshua Columbus4,
- Denise D. Belsham1,2,4,
- David M. Irwin5,
- Haibo Zhang3,
- Xiaoyan Wen2,3,
- Qinghua Wang3,4 and
- Tianru Jin1,2,4,5⇓
- 1Division of Cell and Molecular Biology, Toronto General Research Institute, University Health Network, Toronto, Ontario, Canada
- 2Department of Medicine, University of Toronto, Toronto, Ontario, Canada
- 3Keenan Research Centre, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada
- 4Department of Physiology, University of Toronto, Toronto, Ontario, Canada
- 5Department of Laboratory Medicine and Pathobiology, Toronto Medical Discovery Tower, University Health Network, Toronto, Ontario, Canada
- Corresponding author: Tianru Jin, .
W.S. and D.W. contributed equally to this study.
The type 2 diabetes risk gene TCF7L2 is the effector of the Wnt signaling pathway. We found previously that in gut endocrine L-cell lines, TCF7L2 controls transcription of the proglucagon gene (gcg), which encodes the incretin hormone glucagon-like peptide-1 (GLP-1). Whereas peripheral GLP-1 stimulates insulin secretion, brain GLP-1 controls energy homeostasis through yet-to-be defined mechanisms. We aim to determine the metabolic effect of a functional knockdown of TCF7L2 by generating transgenic mice that express dominant-negative TCF7L2 (TCF7L2DN) specifically in gcg-expressing cells. The gcg-TCF7L2DN transgenic mice showed reduced gcg expression in their gut and brain, but not in pancreas. Defects in glucose homeostasis were observed in these mice, associated with attenuated plasma insulin levels in response to glucose challenge. The defect in glucose disposal was exacerbated with high-fat diet. Brain Wnt activity and feeding-mediated hypothalamic AMP-activated protein kinase (AMPK) repression in these mice were impaired. Peripheral injection of the cAMP-promoting agent forskolin increased brain β-cat Ser675 phosphorylation and brain gcg expression and restored feeding-mediated hypothalamic AMPK repression. We conclude that TCF7L2 and Wnt signaling control gut and brain gcg expression and glucose homeostasis and speculate that positive cross-talk between Wnt and GLP-1/cAMP signaling is an underlying mechanism for brain GLP-1 in exerting its metabolic functions.
This article contains Supplementary Data online at http://diabetes.diabetesjournals.org/lookup/suppl/doi:10.2337/db12-0365/-/DC1.
See accompanying commentary, p. 706.
- Received March 22, 2012.
- Accepted July 4, 2012.
- © 2013 by the American Diabetes Association.
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