Dominant Role of the p110β Isoform of PI3K over p110α in Energy Homeostasis Regulation by POMC and AgRP Neurons
Year: 2009
Type: article
Abstract: PI3K signaling is thought to mediate leptin and insulin action in hypothalamic pro-opiomelanocortin (POMC) and agouti-related protein (AgRP) neurons, key regulators of energy homeostasis, through largely unknown mechanisms. We inactivated either p110alpha or p110beta PI3K catalytic subunits in these neurons and demonstrate a dominant role for the latter in energy homeostasis regulation. In POMC neurons, p110beta inactivation prevented insulin- and leptin-stimulated electrophysiological responses. POMCp110beta null mice exhibited central leptin resistance, increased adiposity, and diet-induced obesity. In contrast, the response to leptin was not blocked in p110alpha-deficient POMC neurons. Accordingly, POMCp110alpha null mice displayed minimal energy homeostasis abnormalities. Similarly, in AgRP neurons, p110beta had a more important role than p110alpha. AgRPp110alpha null mice displayed normal energy homeostasis regulation, whereas AgRPp110beta null mice were lean, with increased leptin sensitivity and resistance to diet-induced obesity. These results demonstrate distinct metabolic roles for the p110alpha and p110beta isoforms of PI3K in hypothalamic energy regulation.
Source: Cell Metabolism
Authors: Hind Al-Qassab, Mark A. Smith, Elaine E. Irvine, Julie Guillermet-Guibert, Marc Claret, Agharul I. Choudhury, Colin Selman, Kaisa Piipari, Melanie Clements, Steven Lingard, Keval Chandarana, Jimmy D. Bell, Gregory S. Barsh, Andrew J.H. Smith, Rachel L. Batterham, Michael L.J. Ashford, Bart Vanhaesebroeck, Dominic J. Withers
Language: English
Subfield: Endocrine and Autonomic Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $10,400
Funders: European Molecular Biology Organization, Queen Mary University of London, Ludwig Institute for Cancer Research, Wellcome Trust, Diabetes UK, European Commission, Fondation pour la Recherche Médicale, Directorate for Biological Sciences, Medical Research Council, Biotechnology and Biological Sciences Research Council
Awards: G1657047212, G8168914681
OpenAlex ID: W2143141103
