Prewitt Amanda K, Wilson Melinda E
Department of Physiology, University of Kentucky College of Medicine, 800 Rose Street, Lexington, KY 40536, USA.
Brain Res. 2007 Feb 23;1134(1):62-9. doi: 10.1016/j.brainres.2006.11.069. Epub 2007 Jan 17.
Estrogen plays a critical role in brain development and is responsible for generating sex differences in cognition and emotion. Studies in rodent models have shown high levels of estrogen binding in non-reproductive areas of the brain during development, including the cortex and hippocampus, yet binding is diminished in the same areas of the adult brain. These binding studies demonstrated that estrogen receptors decline in the cortex during development but did not identify which of the two estrogen receptors was present. In the current study, we examined the expression of estrogen receptor alpha (ERalpha) and estrogen receptor beta (ERbeta) in the mouse cortex during the first month of life. Messenger RNA was isolated from cortical tissue taken from C57BL/6 mice on postnatal day (PND) 1, 4, 10, 18 and 25 and expression levels were determined by real-time PCR. ERalpha mRNA expression in the mouse cortex at PND 25 was significantly reduced as compared to PND 1 (p<0.01). ERbeta mRNA expression at PND 25 was significantly increased as compared to PND 1 (p<0.05). Although the increase in ERbeta mRNA was statistically significant, the ERbeta levels were extremely low in the isocortex compared to ERalpha mRNA levels, suggesting that ERalpha may play a more critical role in the developmental decrease of estradiol binding than ERbeta. Additionally, we measured ERalpha mRNA expression in organotypic explant cultures of cortex taken from PND 3 mice. Explants were maintained in vitro for 3 weeks. mRNA was isolated at several time points and ERalpha and ERbeta mRNA was measured by real-time RT-PCR. ERalpha and ERbeta mRNA levels reflected a similar pattern in vitro and in vivo, suggesting that signals outside the cortex are not needed for this developmental change. This study lays the groundwork for an understanding of the mechanisms of the developmental regulation of ERalpha mRNA.
雌激素在大脑发育中起着关键作用,并且是认知和情感方面性别差异产生的原因。对啮齿动物模型的研究表明,在发育过程中,大脑的非生殖区域(包括皮层和海马体)存在高水平的雌激素结合,但在成年大脑的相同区域,这种结合会减少。这些结合研究表明,发育过程中皮层中的雌激素受体数量会下降,但并未确定存在的是两种雌激素受体中的哪一种。在本研究中,我们检测了出生后第一个月小鼠皮层中雌激素受体α(ERα)和雌激素受体β(ERβ)的表达。从出生后第1天、第4天、第10天、第18天和第25天的C57BL/6小鼠的皮层组织中分离信使核糖核酸,并通过实时聚合酶链反应测定表达水平。与出生后第1天相比,出生后第25天小鼠皮层中的ERα信使核糖核酸表达显著降低(p<0.01)。与出生后第1天相比,出生后第25天的ERβ信使核糖核酸表达显著增加(p<0.05)。尽管ERβ信使核糖核酸的增加具有统计学意义,但与ERα信使核糖核酸水平相比,同型皮层中的ERβ水平极低,这表明与ERβ相比,ERα可能在雌二醇结合的发育性减少中发挥更关键的作用。此外,我们测量了出生后第3天小鼠皮层的器官型外植体培养物中ERα信使核糖核酸的表达。外植体在体外维持3周。在几个时间点分离信使核糖核酸,并通过实时逆转录聚合酶链反应测量ERα和ERβ信使核糖核酸。ERα和ERβ信使核糖核酸水平在体外和体内反映出相似的模式,这表明这种发育变化不需要皮层外的信号。本研究为理解ERα信使核糖核酸发育调控机制奠定了基础。