Beta-cell specific Insr deletion promotes insulin hypersecretion and improves glucose tolerance prior to global insulin resistance

• DOI: 10.1038/s41467-022-28039-8
• Publication Date: 2022-02-08T11:05:07Z
• Authors: Søs Skovsø; Evgeniy Panzhinskiy; Jelena Kolic; Haoning Howard Cen; Derek A. Dionne; Xiao-Qing Dai; Rohit B. Sharma; Lynda Elghazi; Cara E. Ellis; Katharine Faulkner; Stephanie A. M. M...; Peter Overby; Nilou Noursadeghi; Daria Hutchinson; Xiaoke Hu; Hong Li; Honey Modi; Jennifer S. Wildi; J. Diego Botezelli; Hye Lim Noh; Sujin Suk; Brian Gablaski; Austin Bautista; Ryekjang Kim; Corentin Cras-Méneur; Stephane Flibotte; Sunita Sinha; Dan S. Luciani; Corey Nislow; Elizabeth J. Rideout; Eric N. Cytrynbaum; Jason K. Kim; Ernesto Bernal-Mi...; Laura C. Alonso; Patrick E. MacDonald; James D. Johnson
• Keywords: Male; 0301 basic medicine; 570; and Hormone Antagonists; Science; Datasets as Topic; Mice, Transgenic; 612; insulin hypersecretion; Diet, High-Fat; Article; 576; Gene Knockout Techniques; Mice; 03 medical and health sciences; Endocrinology; Sex Factors; insulin resistance; Hyperinsulinism; Insulin-Secreting Cells; Animals; Humans; Insulin; Gene Knock-In Techniques; RNA-Seq; 0303 health sciences; Diabetes; Q; Hormones; Receptor, Insulin; Cellular and Molecular Physiology; Disease Models, Animal; Glucose; Diabetes Mellitus, Type 2; physiology; hyperinsulinemia; Hormone Substitutes; Female; Insulin Resistance; Physiological Processes

AbstractInsulin receptor (Insr) protein is present at higher levels in pancreatic β-cells than in most other tissues, but the consequences of β-cell insulin resistance remain enigmatic. Here, we use an Ins1cre knock-in allele to delete Insr specifically in β-cells of both female and male mice. We compare experimental mice to Ins1cre-containing littermate controls at multiple ages and on multiple diets. RNA-seq of purified recombined β-cells reveals transcriptomic consequences of Insr loss, which differ between female and male mice. Action potential and calcium oscillation frequencies are increased in Insr knockout β-cells from female, but not male mice, whereas only male βInsrKO islets have reduced ATP-coupled oxygen consumption rate and reduced expression of genes involved in ATP synthesis. Female βInsrKO and βInsrHET mice exhibit elevated insulin release in ex vivo perifusion experiments, during hyperglycemic clamps, and following i.p. glucose challenge. Deletion of Insr does not alter β-cell area up to 9 months of age, nor does it impair hyperglycemia-induced proliferation. Based on our data, we adapt a mathematical model to include β-cell insulin resistance, which predicts that β-cell Insr knockout improves glucose tolerance depending on the degree of whole-body insulin resistance. Indeed, glucose tolerance is significantly improved in female βInsrKO and βInsrHET mice compared to controls at 9, 21 and 39 weeks, and also in insulin-sensitive 4-week old males. We observe no improved glucose tolerance in older male mice or in high fat diet-fed mice, corroborating the prediction that global insulin resistance obscures the effects of β-cell specific insulin resistance. The propensity for hyperinsulinemia is associated with mildly reduced fasting glucose and increased body weight. We further validate our main in vivo findings using an Ins1-CreERT transgenic line and find that male mice have improved glucose tolerance 4 weeks after tamoxifen-mediated Insr deletion. Collectively, our data show that β-cell insulin resistance in the form of reduced β-cell Insr contributes to hyperinsulinemia in the context of glucose stimulation, thereby improving glucose homeostasis in otherwise insulin sensitive sex, dietary and age contexts.