4.7 Article

Gpr158 mediates osteocalcin's regulation of cognition

Journal

JOURNAL OF EXPERIMENTAL MEDICINE
Volume 214, Issue 10, Pages 2859-2873

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20171320

Keywords

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Funding

  1. National Institute on Aging [2P01 AG032959-06A1]
  2. Columbia Aging Center
  3. National Institute of Diabetes and Digestive and Kidney Diseases [5T32DK007328-38]
  4. Fondation pour la Recherche Medicale [AJE20130928594]
  5. Career Development Award from the Human Frontier Scientific Program
  6. ATIP-AVE NIR Program of Institut National de la Sante et de la Recherche Medicale
  7. AGE MED Program of Institut National de la Sante et de la Recherche Medicale
  8. Philippe Foundation

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That osteocalcin (OCN) is necessary for hippocampal-dependent memory and to prevent anxiety-like behaviors raises novel questions. One question is to determine whether OCN is also sufficient to improve these behaviors in wild-type mice, when circulating levels of OCN decline as they do with age. Here we show that the presence of OCN is necessary for the beneficial influence of plasma from young mice when injected into older mice on memory and that peripheral delivery of OCN is sufficient to improve memory and decrease anxiety-like behaviors in 16-mo-old mice. A second question is to identify a receptor transducing OCN signal in neurons. Genetic, electrophysiological, molecular, and behavioral assays identify Gpr158, an orphan G protein-coupled receptor expressed in neurons of the CA3 region of the hippocampus, as transducing OCN's regulation of hippocampal-dependent memory in part through inositol 1,4,5-trisphosphate and brain-derived neurotrophic factor. These results indicate that exogenous OCN can improve hippocampal-dependent memory in mice and identify molecular tools to harness this pathway for therapeutic purposes.

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