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Distribution of estrogen receptor β containing cells in the brains of bacterial artificial chromosome transgenic mice.

Teresa A Milner | Louisa I Thompson | Gang Wang | Justin A Kievits | Eugene Martin | Ping Zhou | Bruce S McEwen | Donald W Pfaff | Elizabeth M Waters
Brain research | 2010

In the brain, estrogen receptor beta (ERbeta) plays important roles in autonomic functions, stress reactivity and learning and memory processes. However, understanding the function of ERbeta has been restricted by the limited availability of specific antisera, by difficulties discriminating the discrete localization of ERbeta-immunoreactivity (ir) at the light microscopic level in many brain regions and the identification of ERbeta-containing neurons in neurophysiological and molecular studies. Here, we demonstrate that a Esr2 bacterial artificial chromosome (BAC) transgenic mouse line that expresses ERbeta identified by enhanced green fluorescent protein (EGFP) overcomes these shortcomings. Throughout the brain, ERbeta-EGFP was detected in the nuclei and cytoplasm of cells, the majority of which resembled neurons. EGFP often extended into dendritic processes and could be identified either natively or following intensification of EGFP using immunolabeling. The distribution of ERbeta-EGFP cells in brain closely corresponded to that reported for ERbeta protein and mRNA. In particular, ERbeta-EGFP cells were found in autonomic brain regions (i.e., hypothalamic paraventricular nucleus, rostral ventrolateral medulla and nucleus of the solitary tract), in regions associated with anxiety and stress behaviors (i.e., bed nucleus of the stria terminalis, amygdala, periaqueductal gray, raphe and parabrachial nuclei) and in regions involved in learning and memory processes (i.e., basal forebrain, cerebral cortex and hippocampus). Additionally, dual label light and electron microscopic studies in select brain areas demonstrate that cell containing ERbeta-EGFP colocalize with both nuclear and extranuclear ERbeta-immunoreactivity. These findings support the utility of Esr2 BAC transgenic reporter mice for future studies understanding the role of ERbeta in CNS function.

Pubmed ID: 20599828

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Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: HD0751
  • Agency: NINDS NIH HHS, United States
    Id: NS007080
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA008259
  • Agency: NIA NIH HHS, United States
    Id: P01 AG016765
  • Agency: NIMH NIH HHS, United States
    Id: MH38273
  • Agency: NIA NIH HHS, United States
    Id: AG016765
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD005751-29
  • Agency: NIDA NIH HHS, United States
    Id: DA08259
  • Agency: NHLBI NIH HHS, United States
    Id: HL18974
  • Agency: NHLBI NIH HHS, United States
    Id: HL096571
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS007080
  • Agency: NIA NIH HHS, United States
    Id: P01 AG016765-100001
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS007080-42
  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL018974
  • Agency: NIDDK NIH HHS, United States
    Id: T32 DK007313-32
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL098351
  • Agency: NIDDK NIH HHS, United States
    Id: T32 DK007313
  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL018974-309002
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS007080-43
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH038273-23S1
  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL096571-026274
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD005751
  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL096571
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH038273
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA008259-18
  • Agency: NIDDK NIH HHS, United States
    Id: DK07313

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Gene Expression Nervous System Atlas (tool)

RRID:SCR_002721

Gene expression data and maps of mouse central nervous system. Gene expression atlas of developing adult central nervous system in mouse, using in situ hybridization and transgenic mouse techniques. Collection of pictorial gene expression maps of brain and spinal cord of mouse. Provides tools to catalog, map, and electrophysiologically record individual cells. Application of Cre recombinase technologies allows for cell-specific gene manipulation. Transgenic mice created by this project are available to scientific community.

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