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一种培养形态保持良好的大鼠下丘脑室管膜细胞的简单策略。

A simple strategy for culturing morphologically-conserved rat hypothalamic tanycytes.

机构信息

Laboratory of Neurophysiology of the Multidisciplinary Institute of Cell Biology [IMBICE, dependent of the Argentine Research Council (CONICET) and Scientific Research Commission, Province of Buenos Aires (CIC-PBA)], Calle 526 entre 10 y 11, PO Box 403, La Plata, 1900, Buenos Aires, Argentina.

Cell Culture Facility of the Multidisciplinary Institute of Cell Biology [IMBICE, dependent of the Argentine Research Council (CONICET) and Scientific Research Commission, Province of Buenos Aires (CIC-PBA)], La Plata, Buenos Aires, Argentina.

出版信息

Cell Tissue Res. 2017 Aug;369(2):369-380. doi: 10.1007/s00441-017-2608-x. Epub 2017 Apr 17.

Abstract

Hypothalamic tanycytes are specialized bipolar ependymal cells that line the floor of the third ventricle. Given their strategic location, tanycytes are believed to play several key functions including being a selective barrier and controlling the amount of hypothalamic-derived factors reaching the anterior pituitary. The in vitro culture of these cells has proved to be difficult. Here, we report an improved method for the generation of primary cultures of rat hypothalamic tanycytes. Ependymal cultures were derived from tissue dissected out of the median eminence region of 10-day-old rats and cultured in a chemically defined medium containing DMEM:F12, serum albumin, insulin, transferrin and the antibiotic gentamycin. After 7 days in vitro, ∼30% of the cultured cells exhibited morphological features of tanycytes as observed by phase contrast or scanning electron microscopy. Tanycyte-like cells were strongly immuno-reactive for vimentin and dopamine-cAMP-regulated phospho-protein (DARPP-32) and weakly immune-reactive for glial fibrillary acidic protein. Tanycyte-like cells displayed a stable negative resting plasma membrane potential and failed to show spiking properties in response to current injections. When exposed to fluorescent beads in the culture medium, tanycyte-like cells exhibited a robust endocytosis. Thus, the present method effectively yields cultures containing tanycyte-like cells that resemble in vivo tanycytes in terms of morphologic features and molecular markers as well as electrical and endocytic activity. To our knowledge, this is the first protocol that allows the culturing of tanycyte-like cells that can be individually identified and that conserve the morphology of tanycytes in their natural physiological environment.

摘要

下丘脑的室管膜下细胞(tanycyte)是一种特化的双极室管膜细胞,排列在第三脑室的底部。鉴于其所处的战略位置,tanycyte 被认为发挥着几种关键功能,包括作为选择性屏障和控制到达垂体前叶的下丘脑衍生因子的数量。这些细胞的体外培养已被证明具有一定难度。在这里,我们报告了一种改进的大鼠下丘脑 tanycyte 原代培养方法。室管膜培养物是从 10 天大的大鼠的正中隆起区域分离出来的组织中获得的,并在含有 DMEM:F12、血清白蛋白、胰岛素、转铁蛋白和抗生素庆大霉素的化学定义培养基中培养。在体外培养 7 天后,约 30%的培养细胞表现出 tanycyte 的形态特征,可通过相差或扫描电子显微镜观察到。tanycyte 样细胞强烈免疫反应性地表达波形蛋白和多巴胺-cAMP 调节的磷酸蛋白(DARPP-32),并弱免疫反应性地表达神经胶质纤维酸性蛋白。tanycyte 样细胞显示出稳定的负静息质膜电位,并且在对电流注入的反应中不表现出尖峰特性。当暴露于培养基中的荧光珠时,tanycyte 样细胞表现出强大的内吞作用。因此,本方法有效地产生了含有 tanycyte 样细胞的培养物,这些细胞在形态特征、分子标志物以及电生理和内吞活性方面与体内 tanycyte 相似。据我们所知,这是第一个允许培养可单独鉴定且保留 tanycyte 天然生理环境形态的 tanycyte 样细胞的方案。

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