能分化为神经内分泌细胞的小鼠胎儿下丘脑神经干细胞(AC1)的建立。

Neurogenesis (Austin, Tex.) Pub Date : 2014-07-28 eCollection Date: 2014-01-01 DOI:10.4161/neur.29950
Anna Cariboni, Luciano Conti, Valentina Andrè, Davide Aprile, Jacopo Zasso, Roberto Maggi
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引用次数: 6

摘要

本研究描述了胚胎小鼠下丘脑神经干细胞的生成和稳定细胞系的特征。这些细胞(AC1)在确定的无血清培养基中作为贴壁培养物生长,表达神经源性放射状胶质细胞和下丘脑前体的典型标志物。AC1细胞经长时间扩增后,可在体外有效诱导分化为神经元和星形胶质细胞,并开始表达一些激素神经肽,如TRH、CRH、POMC等。基于AC1细胞在体外稳定扩增和形成神经内分泌谱系的能力,这些细胞可能为阐明下丘脑发育和神经内分泌神经元特异性分化的机制提供了新的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Establishment of a radial glia-like mouse fetal hypothalamic neural stem cell line (AC1) able to differentiate into neuroendocrine cells.

Establishment of a radial glia-like mouse fetal hypothalamic neural stem cell line (AC1) able to differentiate into neuroendocrine cells.

Establishment of a radial glia-like mouse fetal hypothalamic neural stem cell line (AC1) able to differentiate into neuroendocrine cells.

Establishment of a radial glia-like mouse fetal hypothalamic neural stem cell line (AC1) able to differentiate into neuroendocrine cells.

The present study describes the generation and the characterization of a stable cell line of neural stem cells derived from embryonic mouse hypothalamus. These cells (AC1) grow as an adherent culture in defined serum-free medium and express typical markers of neurogenic radial glia and of hypothalamic precursors. After prolonged expansion, AC1 cells may be efficiently induced to differentiate into neurons and astroglial cells in vitro and start to express some hormonal neuropeptides, like TRH, CRH, and POMC. Based on the capabilities of AC1 cells to be stably expanded and to develop neuroendocrine lineages in vitro, these cells might represent a novel tool to elucidate the mechanisms involved in the development of the hypothalamus and in the specific differentiation of neuroendocrine neurons.

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