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Signaling through the M(3) muscarinic receptor favors bone mass accrual by decreasing sympathetic activity.


ABSTRACT: Bone remodeling is regulated by various neuronal inputs, including sympathetic tone, which is known to inhibit bone mass accrual. This aspect of sympathetic nervous system function raises the prospect that the other arm of the autonomic nervous system, the parasympathetic nervous system, may also affect bone remodeling. Here, we use various mutant mouse strains, each lacking one of the muscarinic receptors that mediate parasympathetic activity, to show that the parasympathetic nervous system acting through the M(3) muscarinic receptor is a positive regulator of bone mass accrual, increasing bone formation and decreasing bone resorption. Gene expression studies, cell-specific gene deletion experiments, and analysis of compound mutant mice showed that the parasympathetic nervous system favors bone mass accrual by acting centrally and by decreasing the sympathetic tone. By showing that both arms of the autonomic nervous system affect bone remodeling, this study further underscores the importance of neuronal regulation of bone.

SUBMITTER: Shi Y 

PROVIDER: S-EPMC2832931 | biostudies-literature | 2010 Mar

REPOSITORIES: biostudies-literature

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Signaling through the M(3) muscarinic receptor favors bone mass accrual by decreasing sympathetic activity.

Shi Yu Y   Oury Franck F   Yadav Vijay K VK   Wess Jürgen J   Liu X Sherry XS   Guo X Edward XE   Murshed Monzur M   Karsenty Gerard G  

Cell metabolism 20100301 3


Bone remodeling is regulated by various neuronal inputs, including sympathetic tone, which is known to inhibit bone mass accrual. This aspect of sympathetic nervous system function raises the prospect that the other arm of the autonomic nervous system, the parasympathetic nervous system, may also affect bone remodeling. Here, we use various mutant mouse strains, each lacking one of the muscarinic receptors that mediate parasympathetic activity, to show that the parasympathetic nervous system act  ...[more]

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