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Spatiotemporal Mapping of the Oxytocin Receptor at Single-Cell Resolution in the Postnatally Developing Mouse Brain.
Li, Hao; Li, Ying; Wang, Ting; Li, Shen; Liu, Heli; Ning, Shuyi; Shen, Wei; Zhao, Zhe; Wu, Haitao.
Affiliation
  • Li H; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
  • Li Y; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
  • Wang T; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
  • Li S; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
  • Liu H; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
  • Ning S; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
  • Shen W; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
  • Zhao Z; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
  • Wu H; Department of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China. wuht@bmi.ac.cn.
Neurosci Bull ; 2024 Sep 15.
Article in En | MEDLINE | ID: mdl-39277552
ABSTRACT
The oxytocin receptor (OXTR) has garnered increasing attention for its role in regulating both mature behaviors and brain development. It has been established that OXTR mediates a range of effects that are region-specific or period-specific. However, the current studies of OXTR expression patterns in mice only provide limited help due to limitations in resolution. Therefore, our objective was to generate a comprehensive, high-resolution spatiotemporal expression map of Oxtr mRNA across the entire developing mouse brain. We applied RNAscope in situ hybridization to investigate the spatiotemporal expression pattern of Oxtr in the brains of male mice at six distinct postnatal developmental stages (P7, P14, P21, P28, P42, P56). We provide detailed descriptions of Oxtr expression patterns in key brain regions, including the cortex, basal forebrain, hippocampus, and amygdaloid complex, with a focus on the precise localization of Oxtr+ cells and the variance of expression between different neurons. Furthermore, we identified some neuronal populations with high Oxtr expression levels that have been little studied, including glutamatergic neurons in the ventral dentate gyrus, Vgat+Oxtr+ cells in the basal forebrain, and GABAergic neurons in layers 4/5 of the cortex. Our study provides a novel perspective for understanding the distribution of Oxtr and encourages further investigations into its functions.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Neurosci Bull Journal subject: NEUROLOGIA Year: 2024 Document type: Article Affiliation country: China Country of publication: Singapore

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Neurosci Bull Journal subject: NEUROLOGIA Year: 2024 Document type: Article Affiliation country: China Country of publication: Singapore