Title

Oestrogen receptor α localisation in the prefrontal cortex of three mammalian species

RIS ID

101081

Publication Details

Montague, D., Weickert, C. S., Tomaskovic-Crook, E., Rothmond, D. A., Kleinman, J. E. & Rubinow, D. R. (2008). Oestrogen receptor α localisation in the prefrontal cortex of three mammalian species. Journal of Neuroendocrinology, 20 (7), 893-903.

Abstract

Oestrogen modulates cognitive function and affective behaviours subserved by the prefrontal cortex (PFC). Identifying and localising oestrogen receptor (ER)α, in human PFC will contribute to our understanding of the molecular mechanism of oestrogen action in this region. Inferences about the site of action of oestrogen in human brain are derived largely from studies performed in nonhuman mammalian species; however, the congruence of findings across species has not been demonstrated. Furthermore, the laminar, cellular, and subcellular localisation of ERα in the cortex is debated. Therefore, we compared the distribution of ERα in human dorsolateral prefrontal cortex (DLPFC) with that of monkey DLPFC and rat medial PFC. Immunohistochemistry performed on frontal cortex from the three species demonstrated ERα positive cells throughout all layers of the PFC, in pyramidal and nonpyramidal neurones, with both nuclear and cytoplasmic immunoreactivity. Western blot analyses and preabsorption studies confirmed that the antibody used recognised ERα and not ERβ. A strong ERα immunoreactive band corresponding to the full-length ERα protein (65-67kDa) in the frontal cortex of all three species matched the size of the predominant immunoreactive band detected in breast cancer cell lines known to express ERα. Additionally, other ERα immunoreactive proteins of varying molecular weight in breast cancer cells, rat ovary and mammalian brain were detected, suggesting that ERα may exist in more than one form in the mammalian frontal cortex. The present study provides evidence that ERα protein exists in neurones in mammalian PFC and that ERα is anatomically well-positioned to directly mediate oestrogen action in these neurones.

Please refer to publisher version or contact your library.

Share

COinS
 

Link to publisher version (DOI)

http://dx.doi.org/10.1111/j.1365-2826.2008.01743.x