Abstract
Oestrogen receptors (ERs) are important for sexual differentiation of the brain. Previous studies in rats have reported that the locus coeruleus (LC), a catecholaminergic nucleus in the brain stem, is sexually dimorphic such that females have more neurones than males. We hypothesised that ERs may be important for sexual differentiation of this nucleus in mice. Because previous studies reported conflicting results regarding ER protein expression in the mouse LC, we evaluated ERα and ERβ gene expression by in situ hybridisation and the real-time reverse transcription-polymerase chain reaction. We demonstrated that both ERα and ERβ mRNAs are present in tyrosine hydroxylase-immunoreactive (TH-ir) cells in the male LC. In the female LC, ERα mRNA is present at levels similar to males, whereas ERβ mRNA expression is significantly lower than in males. Similar to rats, male mice have fewer TH-ir cells in the LC than females at 60 days after birth, but the difference is absent at 120 days after birth when females exhibit a similar reduction in TH-ir cells. The transient sex difference is ERβ-dependent because is it absent in ERβ knockout mice, and is due to regulation of TH expression and not from death of TH-ir cells. Testicular hormones produced at adolescence are necessary for the regulation of TH expression in the male LC because orchidectomy of pre-pubertal males prevented the decrease in TH-ir cells, whereas treatment of gonadectomised males with testosterone or its metabolite, 5α-androstan-3β,17β-diol, restored the intact male phenotype. Overall, these studies indicate that ERβ is important in regulating TH expression in the mouse LC.
| Original language | English |
|---|---|
| Pages (from-to) | 1155-1164 |
| Number of pages | 10 |
| Journal | Journal of Neuroendocrinology |
| Volume | 20 |
| Issue number | 10 |
| DOIs | |
| State | Published - Sep 16 2008 |
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Keywords
- Locus coeruleus
- Mouse
- Oestrogen receptor β
- Tyrosine hydroxylase
ASJC Scopus subject areas
- Endocrinology
- Neuroscience(all)
Cite this
Oestrogen receptor β contributes to the transient sex difference in tyrosine hydroxylase expression in the mouse locus coeruleus. / Pendergast, J. S.; Tuesta, L. M.; Bethea, John R.
In: Journal of Neuroendocrinology, Vol. 20, No. 10, 16.09.2008, p. 1155-1164.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Oestrogen receptor β contributes to the transient sex difference in tyrosine hydroxylase expression in the mouse locus coeruleus
AU - Pendergast, J. S.
AU - Tuesta, L. M.
AU - Bethea, John R.
PY - 2008/9/16
Y1 - 2008/9/16
N2 - Oestrogen receptors (ERs) are important for sexual differentiation of the brain. Previous studies in rats have reported that the locus coeruleus (LC), a catecholaminergic nucleus in the brain stem, is sexually dimorphic such that females have more neurones than males. We hypothesised that ERs may be important for sexual differentiation of this nucleus in mice. Because previous studies reported conflicting results regarding ER protein expression in the mouse LC, we evaluated ERα and ERβ gene expression by in situ hybridisation and the real-time reverse transcription-polymerase chain reaction. We demonstrated that both ERα and ERβ mRNAs are present in tyrosine hydroxylase-immunoreactive (TH-ir) cells in the male LC. In the female LC, ERα mRNA is present at levels similar to males, whereas ERβ mRNA expression is significantly lower than in males. Similar to rats, male mice have fewer TH-ir cells in the LC than females at 60 days after birth, but the difference is absent at 120 days after birth when females exhibit a similar reduction in TH-ir cells. The transient sex difference is ERβ-dependent because is it absent in ERβ knockout mice, and is due to regulation of TH expression and not from death of TH-ir cells. Testicular hormones produced at adolescence are necessary for the regulation of TH expression in the male LC because orchidectomy of pre-pubertal males prevented the decrease in TH-ir cells, whereas treatment of gonadectomised males with testosterone or its metabolite, 5α-androstan-3β,17β-diol, restored the intact male phenotype. Overall, these studies indicate that ERβ is important in regulating TH expression in the mouse LC.
AB - Oestrogen receptors (ERs) are important for sexual differentiation of the brain. Previous studies in rats have reported that the locus coeruleus (LC), a catecholaminergic nucleus in the brain stem, is sexually dimorphic such that females have more neurones than males. We hypothesised that ERs may be important for sexual differentiation of this nucleus in mice. Because previous studies reported conflicting results regarding ER protein expression in the mouse LC, we evaluated ERα and ERβ gene expression by in situ hybridisation and the real-time reverse transcription-polymerase chain reaction. We demonstrated that both ERα and ERβ mRNAs are present in tyrosine hydroxylase-immunoreactive (TH-ir) cells in the male LC. In the female LC, ERα mRNA is present at levels similar to males, whereas ERβ mRNA expression is significantly lower than in males. Similar to rats, male mice have fewer TH-ir cells in the LC than females at 60 days after birth, but the difference is absent at 120 days after birth when females exhibit a similar reduction in TH-ir cells. The transient sex difference is ERβ-dependent because is it absent in ERβ knockout mice, and is due to regulation of TH expression and not from death of TH-ir cells. Testicular hormones produced at adolescence are necessary for the regulation of TH expression in the male LC because orchidectomy of pre-pubertal males prevented the decrease in TH-ir cells, whereas treatment of gonadectomised males with testosterone or its metabolite, 5α-androstan-3β,17β-diol, restored the intact male phenotype. Overall, these studies indicate that ERβ is important in regulating TH expression in the mouse LC.
KW - Locus coeruleus
KW - Mouse
KW - Oestrogen receptor β
KW - Tyrosine hydroxylase
UR - http://www.scopus.com/inward/record.url?scp=51449109103&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=51449109103&partnerID=8YFLogxK
U2 - 10.1111/j.1365-2826.2008.01776.x
DO - 10.1111/j.1365-2826.2008.01776.x
M3 - Article
C2 - 18680559
AN - SCOPUS:51449109103
VL - 20
SP - 1155
EP - 1164
JO - Journal of Neuroendocrinology
JF - Journal of Neuroendocrinology
SN - 0953-8194
IS - 10
ER -