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MNAR mRNA在小鼠大脑中的发育表达。

Developmental expression of MNAR mRNA in the mouse brain.

作者信息

Pawlak Justyna, Beyer Cordian

机构信息

Anatomisches Institut, Universität Tübingen, Osterbergstrasse 3, 72074, Tübingen, Germany.

出版信息

Cell Tissue Res. 2005 Jun;320(3):545-9. doi: 10.1007/s00441-005-1090-z. Epub 2005 Apr 22.

Abstract

During the development of the central nervous system, estrogen influences cellular differentiation and determines the functional connectivity of distinct neural networks. Estrogens generally act through nuclear estrogen receptors (ERs). Recent research has additionally revealed rapid estrogen effects requiring the binding of estrogen to membrane/cytoplasmic ERs and the activation of intracellular signaling systems such as the Src/MAPK cascade. The scaffold protein MNAR/PELP1 appears to be the designated functional mediator of such non-genomic estrogen effects between non-nuclear ERs and Src/MAPKs. In this study, we demonstrate the expression and differential regulation of MNAR mRNA in the developing male and female mouse brain by quantitative polymerase chain reaction. In the midbrain and hypothalamus, a gradual decline in MNAR mRNA levels has been observed prenatally with the highest values at embryonic day 15 and lowest at postnatal day 15. In the cortex, mRNA levels do not fluctuate until postnatal day 7 but decrease thereafter. No differences in MNAR expression between sexes have been detected. Analysis of neuronal and astroglia-enriched cell cultures has revealed the presence of MNAR in both cell types.

摘要

在中枢神经系统发育过程中,雌激素影响细胞分化并决定不同神经网络的功能连接。雌激素通常通过核雌激素受体(ERs)发挥作用。最近的研究还揭示了雌激素的快速效应,这需要雌激素与膜/细胞质ERs结合并激活细胞内信号系统,如Src/丝裂原活化蛋白激酶(MAPK)级联反应。支架蛋白MNAR/PELP1似乎是这种非基因组雌激素效应在非核ERs和Src/MAPKs之间的指定功能介质。在本研究中,我们通过定量聚合酶链反应证明了MNAR mRNA在发育中的雄性和雌性小鼠大脑中的表达及差异调节。在中脑和下丘脑,产前观察到MNAR mRNA水平逐渐下降,在胚胎第15天最高,出生后第15天最低。在皮质中,mRNA水平直到出生后第7天才波动,但此后下降。未检测到两性之间MNAR表达的差异。对富含神经元和星形胶质细胞的细胞培养物的分析表明,两种细胞类型中均存在MNAR。

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