| First Author | Becattini B | Year | 2024 |
| Journal | Cell Rep | Volume | 43 |
| Issue | 5 | Pages | 114132 |
| PubMed ID | 38656871 | Mgi Jnum | J:350955 |
| Mgi Id | MGI:7658773 | Doi | 10.1016/j.celrep.2024.114132 |
| Citation | Becattini B, et al. (2024) Adipocyte PI3K links adipostasis with baseline insulin secretion at fasting through an adipoincretin effect. Cell Rep 43(5):114132 |
| abstractText | Insulin-PI3K signaling controls insulin secretion. Understanding this feedback mechanism is crucial for comprehending how insulin functions. However, the role of adipocyte insulin-PI3K signaling in controlling insulin secretion in vivo remains unclear. Using adipocyte-specific PI3Kalpha knockout mice (PI3Kalpha(AdQ)) and a panel of isoform-selective PI3K inhibitors, we show that PI3Kalpha and PI3Kbeta activities are functionally redundant in adipocyte insulin signaling. PI3Kbeta-selective inhibitors have no effect on adipocyte AKT phosphorylation in control mice but blunt it in adipocytes of PI3Kalpha(AdQ) mice, demonstrating adipocyte-selective pharmacological PI3K inhibition in the latter. Acute adipocyte-selective PI3K inhibition increases serum free fatty acid (FFA) and potently induces insulin secretion. We name this phenomenon the adipoincretin effect. The adipoincretin effect operates in fasted mice with increasing FFA and decreasing glycemia, indicating that it is not primarily a control system for blood glucose. This feedback control system defines the rates of adipose tissue lipolysis and chiefly controls basal insulin secretion during fasting. |
