Astrocytic Insulin Signaling Couples Brain Glucose Uptake with Nutrient Availability

نویسندگان

  • Cristina García-Cáceres
  • Carmelo Quarta
  • Luis Varela
  • Yuanqing Gao
  • Tim Gruber
  • Beata Legutko
  • Martin Jastroch
  • Pia Johansson
  • Jovica Ninkovic
  • Chun-Xia Yi
  • Ophelia Le Thuc
  • Klara Szigeti-Buck
  • Weikang Cai
  • Carola W. Meyer
  • Paul T. Pfluger
  • Ana M. Fernandez
  • Serge Luquet
  • Stephen C. Woods
  • Ignacio Torres-Alemán
  • C. Ronald Kahn
  • Magdalena Götz
  • Tamas L. Horvath
  • Matthias H. Tschöp
چکیده

We report that astrocytic insulin signaling co-regulates hypothalamic glucose sensing and systemic glucose metabolism. Postnatal ablation of insulin receptors (IRs) in glial fibrillary acidic protein (GFAP)-expressing cells affects hypothalamic astrocyte morphology, mitochondrial function, and circuit connectivity. Accordingly, astrocytic IR ablation reduces glucose-induced activation of hypothalamic pro-opio-melanocortin (POMC) neurons and impairs physiological responses to changes in glucose availability. Hypothalamus-specific knockout of astrocytic IRs, as well as postnatal ablation by targeting glutamate aspartate transporter (GLAST)-expressing cells, replicates such alterations. A normal response to altering directly CNS glucose levels in mice lacking astrocytic IRs indicates a role in glucose transport across the blood-brain barrier (BBB). This was confirmed in vivo in GFAP-IR KO mice by using positron emission tomography and glucose monitoring in cerebral spinal fluid. We conclude that insulin signaling in hypothalamic astrocytes co-controls CNS glucose sensing and systemic glucose metabolism via regulation of glucose uptake across the BBB.

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عنوان ژورنال:
  • Cell

دوره 166  شماره 

صفحات  -

تاریخ انتشار 2016