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Sex Hormones Regulate SHANK Expression.
Berkel, Simone; Eltokhi, Ahmed; Fröhlich, Henning; Porras-Gonzalez, Diana; Rafiullah, Rafiullah; Sprengel, Rolf; Rappold, Gudrun A.
Affiliation
  • Berkel S; Department of Human Molecular Genetics, Institute of Human Genetics, Ruprecht-Karls-University, Heidelberg, Germany.
  • Eltokhi A; Department of Human Molecular Genetics, Institute of Human Genetics, Ruprecht-Karls-University, Heidelberg, Germany.
  • Fröhlich H; Research Group of the Max Planck Institute for Medical Research at the Institute of Anatomy and Cell Biology, Ruprecht-Karls-University, Heidelberg, Germany.
  • Porras-Gonzalez D; Department of Human Molecular Genetics, Institute of Human Genetics, Ruprecht-Karls-University, Heidelberg, Germany.
  • Rafiullah R; Department of Human Molecular Genetics, Institute of Human Genetics, Ruprecht-Karls-University, Heidelberg, Germany.
  • Sprengel R; Department of Human Molecular Genetics, Institute of Human Genetics, Ruprecht-Karls-University, Heidelberg, Germany.
  • Rappold GA; Research Group of the Max Planck Institute for Medical Research at the Institute of Anatomy and Cell Biology, Ruprecht-Karls-University, Heidelberg, Germany.
Front Mol Neurosci ; 11: 337, 2018.
Article in En | MEDLINE | ID: mdl-30319350
Autism spectrum disorders (ASD) have a higher prevalence in male individuals compared to females, with a ratio of affected boys compared to girls of 4:1 for ASD and 11:1 for Asperger syndrome. Mutations in the SHANK genes (comprising SHANK1, SHANK2 and SHANK3) coding for postsynaptic scaffolding proteins have been tightly associated with ASD. As early brain development is strongly influenced by sex hormones, we investigated the effect of dihydrotestosterone (DHT) and 17ß-estradiol on SHANK expression in a human neuroblastoma cell model. Both sex hormones had a significant impact on the expression of all three SHANK genes, which could be effectively blocked by androgen and estrogen receptor antagonists. In neuron-specific androgen receptor knock-out mice (Ar NesCre), we found a nominal significant reduction of all Shank genes at postnatal day 7.5 in the cortex. In the developing cortex of wild-type (WT) CD1 mice, a sex-differential protein expression was identified for all Shanks at embryonic day 17.5 and postnatal day 7.5 with significantly higher protein levels in male compared to female mice. Together, we could show that SHANK expression is influenced by sex hormones leading to a sex-differential expression, thus providing novel insights into the sex bias in ASD.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Front Mol Neurosci Year: 2018 Document type: Article Affiliation country: Germany Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Front Mol Neurosci Year: 2018 Document type: Article Affiliation country: Germany Country of publication: Switzerland