Journal
DIABETES
Volume 64, Issue 11, Pages 3829-3838Publisher
AMER DIABETES ASSOC
DOI: 10.2337/db15-0465
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Funding
- U.S. Department of Veterans Affairs [1BX000990-01A1]
- JDRF [3-2010-563]
- National Cancer Institute (Integrated Biological Systems Training in Oncology Training Grant) [5T32 CA119925]
- National Institute of Diabetes and Digestive and Kidney Diseases [DK-97392]
- National Institutes of Health (NIH) [DK-20593]
- NIH [DK-20593, CA-68485, DK-58404, DK-59637, EY-08126]
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Type 2 diabetes incidence increases with age, while beta-cell replication declines. The transcription factor FoxM1 is required for beta-cell replication in various situations, and its expression declines with age. We hypothesized that increased FoxM1 activity in aged beta-cells would rejuvenate proliferation. Induction of an activated form of FoxM1 was sufficient to increase beta-cell mass and proliferation in 12-month-old male mice after just 2 weeks. Unexpectedly, at 2 months of age, induction of activated FoxM1 in male mice improved glucose homeostasis with unchanged beta-cell mass. Cells expressing activated FoxM1 demonstrated enhanced glucose-stimulated Ca2+ influx, which resulted in improved glucose tolerance through enhanced beta-cell function. Conversely, our laboratory has previously demonstrated that mice lacking FoxM1 in the pancreas display glucose intolerance or diabetes with only a 60% reduction in beta-cell mass, suggesting that the loss of FoxM1 is detrimental to beta-cell function. Ex vivo insulin secretion was therefore examined in size-matched islets from young mice lacking FoxM1 in beta-cells. Foxm1-deficient islets indeed displayed reduced insulin secretion. Our studies reveal that activated FoxM1 increases beta-cell replication while simultaneously enhancing insulin secretion and improving glucose homeostasis, making FoxM1 an attractive therapeutic target for diabetes.
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