小鼠出生后视网膜发育过程中 G 蛋白偶联雌激素受体的表达

Wendy L. Piñon-Teal, Judith Mosinger Ogilvie
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引用次数: 0

摘要

雌激素已成为视网膜中的一种多层面信号分子,在神经发育和成人神经保护中发挥着重要作用。它与两种类型的受体相互作用:经典的雌激素受体(ER)α 和β,以及 G 蛋白偶联雌激素受体(Gper)。Gper 在结构、定位和信号传导方面与传统雌激素受体不同。我们应用 qRT-PCR 技术测定了 P0-P21 期野生型小鼠视网膜中 Gper 转录本的表达。在出生后的发育过程中,Gper的表达量增加了6倍,在P14达到高峰。Gper的相对总表达量在视网膜发育过程中出现了显著下降,但不同形式的蛋白质在变化时间上出现了差异。Gper免疫反应可见于视网膜神经节细胞(RGC)的整个发育过程,也可见于早期水平细胞位置的体节。总之,我们的研究阐明了Gper在小鼠视网膜发育过程中的空间和时间表达模式,为进一步研究Gper在视网膜发育和退化过程中的作用奠定了重要基础。
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G protein-coupled estrogen receptor expression in postnatal developing mouse retina
Estrogen has emerged as a multifaceted signaling molecule in the retina, playing an important role in neural development and providing neuroprotection in adults. It interacts with two receptor types: classical estrogen receptors (ERs) alpha and beta, and G protein-coupled estrogen receptor (Gper). Gper differs from classical ERs in structure, localization, and signaling. Here we provide the first report of the temporal and spatial properties of Gper transcript and protein expression in the developing and mature mouse retina.We applied qRT-PCR to determine Gper transcript expression in wild type mouse retina from P0-P21. Immunohistochemistry and Western blot were used to determine Gper protein expression and localization at the same time points.Gper expression showed a 6-fold increase during postnatal development, peaking at P14. Relative total Gper expression exhibited a significant decrease during retinal development, although variations emerged in the timing of changes among different forms of the protein. Gper immunoreactivity was seen in retinal ganglion cells (RGCs) throughout development and also in somas in the position of horizontal cells at early time points. Immunoreactivity was observed in the cytoplasm and Golgi at all time points, in the nucleus at early time points, and in RGC axons as the retina matured.In conclusion, our study illuminates the spatial and temporal expression patterns of Gper in the developing mouse retina and provides a vital foundation for further investigations into the role of Gper in retinal development and degeneration.
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