PI3Kγ ablation does not promote diabetes in db/db mice, but improves insulin sensitivity and reduces pancreatic β‐cell apoptosis. Issue 1 (13th September 2017)

• Record Type: Journal Article
• Authors: Breasson, Ludovic; Sardi, Claudia; Becattini, Barbara; Zani, Fabio; Solinas, Giovanni
• Is Part Of: FASEB journal. Volume 32:Issue 1(2018)
• Page Start: 319
• Page End: 329
• Publication Date: 2017-09-13
• Subjects: phosphoinositide 3‐kinase -- macrophage activation -- neutrophils; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201700372RR
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract : PI3Kγ has emerged as a promising target for the treatment of obesity and insulin resistance; however, previous studies have indicated that PI3Kγ activity in pancreatic β cells is required for normal insulin secretion in response to glucose. Hence, a possible deterioration of insulin secretion capacity in patients who are predisposed to the failure of pancreatic β‐cell function is a major concern for the pharmacologic inhibition of PI3Kγ. To address this issue, we investigated the effects of PI3Kγ ablation in db/db diabetic mice, a genetic model of obesity‐driven β‐cell failure and diabetes. Mice that lacked PI3Kγ were backcrossed into db/+ mice C57BL/KS (>10 generations) to obtain db/db‐PI3Kγ‐/‐ mice. db/db‐PI3Kγ‐/‐ mice and control db/db mice were phenotyped for glucose homeostasis, insulin sensitivity, insulin secretion, steatosis, metabolic inflammation, pancreatic islet morphometry, islet cellular composition, and inflammation. Pancreatic p‐cell apoptosis and proliferation were also evaluated. db/db‐PI3K γ‐/‐ mice and control db/db mice developed similar body weight, steatosis, glycemia, and insulin levels after a glucose load; however, db/db‐PI3Kγ‐/‐ mice displayed improved insulin tolerance, higher levels of fasting serum insulin, and lower pancreatic insulin content. In db/db‐PI3Kγ‐/‐ mice, the number of adipose tissue macrophages was similar to control, but displayed reduced adipose tissue neutrophils and M2‐polarized adipose tissue gene expression. Finally, db/db‐PI3K γ‐/‐ mice have more pancreatic β cells and larger islets than db/db mice, despite displaying similar islet inflammation. This phenotype could be explained by reduced β‐cell apoptosis in db/db‐PI3K γ‐/‐ mice compared with control db/db mice. Our results are consistent with the concept that the beneficial action of PI3Kγ ablation in obesity‐driven glucose intolerance is largely a result of its leptin‐dependent effects on adiposity and, to a lesser extent, the promotion of adipose tissue neutrophil recruitment and M1 polarization of gene expression. Of importance, our data challenge the concept that PI3Kγ is required for insulin secretion in response to glucose in vivo, and indicate that PI3Kγ ablation protects db/db mice from β‐cell apoptosis and improves fasting insulin levels. We conclude that PI3Kγ inhibition in obese patients who are predisposed to β‐cell failure is not expected to produce adverse effects on insulin secretion.—Breasson, L., Sardi, C., Becattini, B., Zani, F., Solinas, G. PI3Kγ ablation does not promote diabetes in db/db mice, but improves insulin sensitivity and reduces pancreatic β‐cell apoptosis. FASEB J. 32, 319‐329 (2018). www.fasebj.org