Cargando…

BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice

Exposure to exercise or to environmental enrichment increases the generation of new neurons in the adult hippocampus and promotes certain kinds of learning and memory. While the precise role of neurogenesis in cognition has been debated intensely, comparatively few studies have addressed the mechani...

Descripción completa

Detalles Bibliográficos
Autores principales: Gobeske, Kevin T., Das, Sunit, Bonaguidi, Michael A., Weiss, Craig, Radulovic, Jelena, Disterhoft, John F., Kessler, John A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759555/
https://www.ncbi.nlm.nih.gov/pubmed/19841742
http://dx.doi.org/10.1371/journal.pone.0007506
_version_ 1782172684273057792
author Gobeske, Kevin T.
Das, Sunit
Bonaguidi, Michael A.
Weiss, Craig
Radulovic, Jelena
Disterhoft, John F.
Kessler, John A.
author_facet Gobeske, Kevin T.
Das, Sunit
Bonaguidi, Michael A.
Weiss, Craig
Radulovic, Jelena
Disterhoft, John F.
Kessler, John A.
author_sort Gobeske, Kevin T.
collection PubMed
description Exposure to exercise or to environmental enrichment increases the generation of new neurons in the adult hippocampus and promotes certain kinds of learning and memory. While the precise role of neurogenesis in cognition has been debated intensely, comparatively few studies have addressed the mechanisms linking environmental exposures to cellular and behavioral outcomes. Here we show that bone morphogenetic protein (BMP) signaling mediates the effects of exercise on neurogenesis and cognition in the adult hippocampus. Elective exercise reduces levels of hippocampal BMP signaling before and during its promotion of neurogenesis and learning. Transgenic mice with decreased BMP signaling or wild type mice infused with a BMP inhibitor both exhibit remarkable gains in hippocampal cognitive performance and neurogenesis, mirroring the effects of exercise. Conversely, transgenic mice with increased BMP signaling have diminished hippocampal neurogenesis and impaired cognition. Exercise exposure does not rescue these deficits, suggesting that reduced BMP signaling is required for environmental effects on neurogenesis and learning. Together, these observations show that BMP signaling is a fundamental mechanism linking environmental exposure with changes in cognitive function and cellular properties in the hippocampus.
format Text
id pubmed-2759555
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-27595552009-10-20 BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice Gobeske, Kevin T. Das, Sunit Bonaguidi, Michael A. Weiss, Craig Radulovic, Jelena Disterhoft, John F. Kessler, John A. PLoS One Research Article Exposure to exercise or to environmental enrichment increases the generation of new neurons in the adult hippocampus and promotes certain kinds of learning and memory. While the precise role of neurogenesis in cognition has been debated intensely, comparatively few studies have addressed the mechanisms linking environmental exposures to cellular and behavioral outcomes. Here we show that bone morphogenetic protein (BMP) signaling mediates the effects of exercise on neurogenesis and cognition in the adult hippocampus. Elective exercise reduces levels of hippocampal BMP signaling before and during its promotion of neurogenesis and learning. Transgenic mice with decreased BMP signaling or wild type mice infused with a BMP inhibitor both exhibit remarkable gains in hippocampal cognitive performance and neurogenesis, mirroring the effects of exercise. Conversely, transgenic mice with increased BMP signaling have diminished hippocampal neurogenesis and impaired cognition. Exercise exposure does not rescue these deficits, suggesting that reduced BMP signaling is required for environmental effects on neurogenesis and learning. Together, these observations show that BMP signaling is a fundamental mechanism linking environmental exposure with changes in cognitive function and cellular properties in the hippocampus. Public Library of Science 2009-10-20 /pmc/articles/PMC2759555/ /pubmed/19841742 http://dx.doi.org/10.1371/journal.pone.0007506 Text en Gobeske et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gobeske, Kevin T.
Das, Sunit
Bonaguidi, Michael A.
Weiss, Craig
Radulovic, Jelena
Disterhoft, John F.
Kessler, John A.
BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice
title BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice
title_full BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice
title_fullStr BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice
title_full_unstemmed BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice
title_short BMP Signaling Mediates Effects of Exercise on Hippocampal Neurogenesis and Cognition in Mice
title_sort bmp signaling mediates effects of exercise on hippocampal neurogenesis and cognition in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759555/
https://www.ncbi.nlm.nih.gov/pubmed/19841742
http://dx.doi.org/10.1371/journal.pone.0007506
work_keys_str_mv AT gobeskekevint bmpsignalingmediateseffectsofexerciseonhippocampalneurogenesisandcognitioninmice
AT dassunit bmpsignalingmediateseffectsofexerciseonhippocampalneurogenesisandcognitioninmice
AT bonaguidimichaela bmpsignalingmediateseffectsofexerciseonhippocampalneurogenesisandcognitioninmice
AT weisscraig bmpsignalingmediateseffectsofexerciseonhippocampalneurogenesisandcognitioninmice
AT radulovicjelena bmpsignalingmediateseffectsofexerciseonhippocampalneurogenesisandcognitioninmice
AT disterhoftjohnf bmpsignalingmediateseffectsofexerciseonhippocampalneurogenesisandcognitioninmice
AT kesslerjohna bmpsignalingmediateseffectsofexerciseonhippocampalneurogenesisandcognitioninmice