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新生大鼠脑的增殖区表达表皮生长因子受体信使核糖核酸。

Proliferative zones of postnatal rat brain express epidermal growth factor receptor mRNA.

作者信息

Seroogy K B, Gall C M, Lee D C, Kornblum H I

机构信息

Department of Anatomy and Neurobiology, University of Kentucky College of Medicine, Lexington 40536-0084, USA.

出版信息

Brain Res. 1995 Jan 23;670(1):157-64. doi: 10.1016/0006-8993(94)01300-7.

DOI:10.1016/0006-8993(94)01300-7
PMID:7719717
Abstract

Two ligands for the epidermal growth factor receptor (EGF-R), EGF and transforming growth factor-alpha (TGF alpha), have recently been shown to influence the proliferation, differentiation or survival of diverse populations of fetal and neonatal neuronal and glial cells in culture. These findings suggest that EGF, TGF alpha, or another EGF-R ligand play a role in the regulation of similar cellular developmental events in vivo. In the present study, in situ hybridization with an 35S-labeled cRNA probe was used to determine if mRNA for EGF-R is expressed in two principal germinal zones of the postnatal rat brain, the forebrain ventricular/subventricular zone and the cerebellar external granule layer. Cells labeled with the EGF-R cRNA were distributed throughout the subventricular zone, particularly in the dorsolateral aspect, from birth to adulthood, although the numbers of labeled cells as well as the density of hybridization diminished during development. In the developing cerebellum, virtually all cells in the external granule layer were densely labeled with the EGF-R cRNA, as were numerous perikarya throughout the molecular layer. EGF-R mRNA was also transiently expressed at lower levels by neurons of the internal granule layer and deep cerebellar nuclei. By adulthood, cerebellar expression of EGF-R mRNA was not detected. These results demonstrate prominent expression of EGF-R mRNA within germinal zones of the developing brain and indicate a role for EGF, TGF alpha, or another member of the EGF-related family in regulating the activities of neuronal and glial progenitor cells in vivo.

摘要

表皮生长因子受体(EGF-R)的两种配体,即表皮生长因子(EGF)和转化生长因子-α(TGFα),最近已被证明可影响培养中的胎儿和新生儿神经元及神经胶质细胞不同群体的增殖、分化或存活。这些发现表明,EGF、TGFα或另一种EGF-R配体在体内类似细胞发育事件的调节中发挥作用。在本研究中,使用35S标记的cRNA探针进行原位杂交,以确定EGF-R的mRNA是否在出生后大鼠脑的两个主要生发区,即前脑室下区/室管膜下区和小脑外颗粒层中表达。从出生到成年,用EGF-R cRNA标记的细胞分布在整个室管膜下区,特别是在背外侧,尽管标记细胞的数量以及杂交密度在发育过程中有所减少。在发育中的小脑中,几乎所有外颗粒层中的细胞都被EGF-R cRNA密集标记,整个分子层中的许多核周体也是如此。内颗粒层和小脑深部核团的神经元也短暂地以较低水平表达EGF-R mRNA。到成年时未检测到小脑EGF-R mRNA的表达。这些结果证明了EGF-R mRNA在发育中脑的生发区内显著表达,并表明EGF、TGFα或EGF相关家族的另一个成员在体内调节神经元和神经胶质祖细胞的活动中发挥作用。

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