Suppr超能文献

发育过程中神经细胞中Id1、Id2和Id3基因的表达。

Id1, Id2, and Id3 gene expression in neural cells during development.

作者信息

Tzeng S F, de Vellis J

机构信息

Department of Neurobiology, Mental Retardation Research Center, Neuropsychiatric Institute, UCLA School of Medicine, Los Angeles, California, USA.

出版信息

Glia. 1998 Dec;24(4):372-81. doi: 10.1002/(sici)1098-1136(199812)24:4<372::aid-glia2>3.0.co;2-b.

Abstract

Id1, Id2, and Id3 mRNA are expressed mainly in the proliferating ependymal cell zone of the mouse brain during embryogenesis. In this study, the expression pattern and cell phenotypes of the Id family mRNA were examined in postnatal and adult rat brain. The expression of Idl and Id3 mRNA in rat brain was observed in the cortex layer 1, corpus callosum, ventricular/subventricular zone (VZ/ SVZ), and the CA1-4 layers of the hippocampus at postnatal day 1 (P1) through P14, whereby it declined at 2 months. In general, the developmental pattern of Idl mRNA coincided with the pattern observed for Id3 mRNA. Similar to Id1 and Id3, Id2 mRNA was highly expressed in the corpus callosum, VZ/SVZ, and the hippocampus. Examination of Id2 mRNA revealed high levels in the cortex and caudate putamen at P1 through P14, whereas a decline was observed in its expression in the adult cortex. In P5 rat cerebellum, all Id mRNA examined were found in the internal granular cell layers; however, at this time point, only Id2 mRNA expression was detected in the differentiating zone of the external granular cell layers, preferentially localizing to adult Purkinje cells. Furthermore, only Id2 mRNA expression in brain was observed in NF+ neurons at P5. Examination of S100alpha+ and GFAP+ astrocytes, revealed the presence of all three mRNAs, whereas the expression of Id2 and Id3 mRNA was absent in 04+ immature oligodendrocytes. These data suggest that the spatial and temporal kinetic patterns during development, as well as cellular specificity, of the Id gene family may play a critical role in neural precursor cell proliferation and cell divergence.

摘要

Id1、Id2和Id3信使核糖核酸在胚胎发育期间主要表达于小鼠脑的增殖室管膜细胞区。在本研究中,对出生后及成年大鼠脑内Id家族信使核糖核酸的表达模式和细胞表型进行了检测。出生后第1天(P1)至P14期间,在大鼠脑的皮质第1层、胼胝体、脑室/室下区(VZ/SVZ)以及海马的CA1-4层观察到Id1和Id3信使核糖核酸的表达,在2个月时表达下降。总体而言,Id1信使核糖核酸的发育模式与Id3信使核糖核酸的模式一致。与Id1和Id3相似,Id2信使核糖核酸在胼胝体、VZ/SVZ和海马中高表达。对Id2信使核糖核酸的检测显示,在P1至P14期间皮质和尾状壳核中水平较高,而在成年皮质中其表达下降。在P5大鼠小脑中,所有检测的Id信使核糖核酸均存在于内颗粒细胞层;然而,在这个时间点,仅在外部颗粒细胞层的分化区检测到Id2信使核糖核酸的表达,且优先定位于成年浦肯野细胞。此外,在P5时仅在NF+神经元中观察到脑内Id2信使核糖核酸的表达。对S100α+和GFAP+星形胶质细胞的检测显示,所有三种信使核糖核酸均存在,而在O4+未成熟少突胶质细胞中不存在Id2和Id3信使核糖核酸的表达。这些数据表明,Id基因家族在发育过程中的时空动力学模式以及细胞特异性可能在神经前体细胞增殖和细胞分化中起关键作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验