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Front Mol Neurosci. 2018 Feb 20;11:28. doi: 10.3389/fnmol.2018.00028. eCollection 2018.

Persistent Expression of Serotonin Receptor 5b Alters Breathing Behavior in Male MeCP2 Knockout Mice.

Frontiers in molecular neuroscience

Steffen Vogelgesang, Marcus Niebert, Anne M Bischoff, Swen Hülsmann, Till Manzke

Affiliations

  1. DFG-Research Center Nanoscale Microscopy and Molecular Physiology of the Brain (CNMPB), University of Göttingen, Göttingen, Germany.
  2. Institute of Neuro- and Sensory Physiology, University of Göttingen, Göttingen, Germany.
  3. Clinic for Anesthesiology, University Medical Göttingen, Göttingen, Germany.

PMID: 29515365 PMCID: PMC5826236 DOI: 10.3389/fnmol.2018.00028

Abstract

Mutations in the transcription factor methyl-CpG-binding protein 2 (MeCP2) cause the neurodevelopmental disorder Rett syndrome (RTT). Besides many other neurological problems, RTT patients show irregular breathing with recurrent apneas or breath-holdings. MeCP2-deficient mice, which recapitulate this breathing phenotype, show a dysregulated, persistent expression of G-protein-coupled serotonin receptor 5-ht

Keywords: 5-ht5b receptor; GPCR; MeCP2; Rett syndrome; breathing disturbances; cAMP regulation

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