首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Arrestin2 expression selectively increases during neural differentiation.
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Arrestin2 expression selectively increases during neural differentiation.

机译:在神经分化过程中,arrestin2表达选择性增加。

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摘要

Arrestins and G protein-coupled receptor kinases (GRKs) are key players in homologous desensitization of G protein-coupled receptors. Two non-visual arrestins, arrestin2 and 3, and five GRKs (GRK2, 3, 4, 5 and 6) are involved in desensitization of many receptors. Here, we demonstrate a steady increase in arrestin2 expression during prenatal development. The density of arrestin2 mRNA is higher in differentiated areas as compared with proliferative zones, whereas arrestin3 mRNA shows the opposite distribution. At embryonic day 14, concentrations of arrestin proteins are similar (32-34 nM). Later in development, arrestin2 expression rises, leading to a fourfold excess of arrestin2 over arrestin3 at birth (48 vs. 11 ng/mg protein or 102 vs. 25 nM). Among GRKs, only GRK5 increased with embryonic age from 124 nm at E14 to 359 nM at birth. Similarly, in vitro differentiation of cultured precursor cells, neurospheres, leads to a significant up-regulation of arrestin2 resulting in > 20-fold excess of arrestin2 (160 vs. 7 nM). GRK5 is the only subtype increased with neurosphere differentiation, although the change is only about twofold. The data demonstrate selective increases in the expression of arrestin2 associated with neural development and suggest specific yet unappreciated roles for arrestin2 in neural differentiation.
机译:Arrestins和G蛋白偶联受体激酶(GRKs)是G蛋白偶联受体同源脱敏的关键因素。两种非视觉抑制蛋白,restarin2和3,以及五个GRK(GRK2、3、4、5和6)与许多受体的脱敏有关。在这里,我们证明了产前发育过程中restarin2表达的稳定增加。与增生区相比,分化区域内的restarin2 mRNA密度更高,而restinin3 mRNA显示相反的分布。在胚胎第14天,抑制素蛋白的浓度相似(32-34 nM)。在后来的发展中,抑制素2的表达增加,导致其在出生时比抑制素3高出四倍(48 vs. 11 ng / mg蛋白或102 vs. 25 nM)。在GRK中,只有GRK5随着胚胎年龄的增加而从E14的124 nm增加到出生时的359 nM。类似地,培养的前体细胞神经球的体外分化会导致restarin2显着上调,导致restin2过量> 20倍(160 vs. 7 nM)。 GRK5是唯一随着神经球分化而增加的亚型,尽管变化仅约两倍。数据表明与神经发育相关的抑制蛋白2的表达选择性增加,并表明抑制蛋白2在神经分化中的特定但尚未意识到的作用。

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