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室旁核前部腹侧中CREB磷酸化的激素调节

Hormonal regulation of CREB phosphorylation in the anteroventral periventricular nucleus.

作者信息

Gu G, Rojo A A, Zee M C, Yu J, Simerly R B

机构信息

Division of Neuroscience, Oregon Regional Primate Research Center, Beaverton, 97006, USA.

出版信息

J Neurosci. 1996 May 1;16(9):3035-44. doi: 10.1523/JNEUROSCI.16-09-03035.1996.

Abstract

The anteroventral periventricular nucleus (AVPV) is a nodal point in neural circuits regulating secretion of gonadotropin and contains sexually dimorphic populations of hormonally regulated dopamine-, dynorphin-, and enkephalin-containing neurons. Because the tyrosine hydroxylase (TH), prodynorphin (PDYN), and proenkephalin (PENK) genes contain cAMP response elements that control their expression in their promoters, we used histochemical methods to determine whether ovarian steroids alter expression of the cAMP response element-binding protein (CREB) in the AVPV. Because the ability of CREB to activate transcription depends on phosphorylation at Ser133, we also evaluated the effects of acute steroid treatment on levels of phosphorylated CREB (pCREB) in AVPV neurons by using an antibody that differentiates between CREB and pCREB. Treatment of ovariectomized rats with estradiol treatments caused a significant induction in the number of pCREB-immunoreactive nuclei within 30 min that was maintained for at least 4 hr, but did not alter CREB immunostaining in the AVPV. Pretreatment with the estrogen antagonist Nafoxidine blocked this induction. In contrast, acute administration of progesterone to estrogen-primed animals suppressed and then increased pCREB staining in the ASVPV at 30 and 60 min, respectively; no significant differences between experimental and control animals were apparent by 2 hr after progesterone treatment. Double-labeling experiments showed that pCREB was colocalized with PDYN, PENK, or TH mRNA in the AVPV, suggesting that pCREB may mediate the effect of steroid hormones on gene expression in these neurons.

摘要

室周前腹侧核(AVPV)是调节促性腺激素分泌的神经回路中的一个节点,包含激素调节的多巴胺能、强啡肽能和脑啡肽能神经元的性别二态性群体。由于酪氨酸羟化酶(TH)、前强啡肽原(PDYN)和前脑啡肽原(PENK)基因在其启动子中含有控制其表达的cAMP反应元件,我们使用组织化学方法来确定卵巢类固醇是否会改变AVPV中cAMP反应元件结合蛋白(CREB)的表达。由于CREB激活转录的能力取决于丝氨酸133处的磷酸化,我们还使用一种能区分CREB和磷酸化CREB的抗体,评估了急性类固醇处理对AVPV神经元中磷酸化CREB(pCREB)水平的影响。用雌二醇处理去卵巢大鼠,在30分钟内导致pCREB免疫反应性细胞核数量显著增加,并持续至少4小时,但未改变AVPV中的CREB免疫染色。用雌激素拮抗剂那法唑酮预处理可阻断这种增加。相反,对用雌激素预处理的动物急性给予孕酮,分别在30分钟和60分钟时抑制并随后增加了ASVPV中的pCREB染色;孕酮处理后2小时,实验动物和对照动物之间没有明显差异。双重标记实验表明,pCREB与AVPV中的PDYN、PENK或TH mRNA共定位,表明pCREB可能介导类固醇激素对这些神经元基因表达的影响。

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本文引用的文献

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Estimation of nuclear population from microtome sections.从切片估计核数量。
Anat Rec. 1946 Feb;94:239-47. doi: 10.1002/ar.1090940210.
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