Journal
PLOS ONE
Volume 8, Issue 5, Pages -Publisher
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0062012
Keywords
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Categories
Funding
- National Institutes of Health (NIH) [DK006181, NIH DK00618146S1, DK07296]
- NIH Washington University Diabetes Research Center Morphology and Metabolic Analysis Core [DK20579]
- American Diabetes Association Grant [7-04-MN-32]
- BarnesJewish Hospital Foundation [7401-00]
- National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
- Juvenile Diabetes Research Foundation International (JDRFI) [JDRF-31-2008-382]
- MSDC
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Major bottlenecks in the expansion of human beta-cell mass are limited proliferation, loss of beta-cell phenotype, and increased apoptosis. In our previous studies, activation of Wnt and mTOR signaling significantly enhanced human beta-cell proliferation. However, isolated human islets displayed insulin signaling pathway resistance, due in part to chronic activation of mTOR/S6K1 signaling that results in negative feedback of the insulin signaling pathway and a loss of Akt phosphorylation and insulin content. We evaluated the effects of a new generation insulin sensitizer, MSDC-0160, on restoring insulin/IGF-1 sensitivity and insulin content in human beta-cells. This novel TZD has low affinity for binding and activation of PPARc and has insulin-sensitizing effects in mouse models of diabetes and ability to lower glucose in Phase 2 clinical trials. MSDC-0160 treatment of human islets increased AMPK activity and reduced mTOR activity. This was associated with the restoration of IGF-1-induced phosphorylation of Akt, GSK-3, and increased protein expression of Pdx1. Furthermore, MSDC-0160 in combination with IGF-1 and 8 mM glucose increased b-cell specific gene expression of insulin, pdx1, nkx6.1, and nkx2.2, and maintained insulin content without altering glucose-stimulated insulin secretion. Human islets were unable to simultaneously promote DNA synthesis and maintain the beta-cell phenotype. Lithium-induced GSK-3 inhibition that promotes DNA synthesis blocked the ability of MSDC-0160 to maintain the beta-cell phenotype. Conversely, MSDC-0160 prevented an increase in DNA synthesis by blocking beta-catenin nuclear translocation. Due to the counteracting pathways involved in these processes, we employed a sequential ex vivo strategy to first induce human islet DNA synthesis, followed by MSDC-0160 to promote the beta-cell phenotype and insulin content. This new generation PPARc sparing insulin sensitizer may provide an initial tool for relieving inherent human islet insulin signaling pathway resistance that is necessary to preserve the beta-cell phenotype during b-cell expansion for the treatment of diabetes.
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