Institute of Human Genetics, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Center for Molecular Medicine Cologne (CMMC), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Methods Mol Biol. 2024;2754:507-519. doi: 10.1007/978-1-0716-3629-9_29.
Primary murine neurons are a well-established tool for investigating Tau in the context of neuronal development and neurodegeneration. However, culturing primary neurons is usually time-consuming and requires multiple feeding steps, media exchanges, proprietary media supplements, and/or preparation of complex media. Here, we describe (i) a relatively cheap and easy cell culture procedure for the cultivation of forebrain neurons from embryonic mice (E13.5) based on a commercially available neuronal supplement (NS21), (ii) a protocol for the cultivation of hippocampal and cortical neurons from postnatal (P0-P3) animals, and (iii) basic fixation and immunofluorescence techniques for the staining of neuronal markers and endogenous Tau. We demonstrate a staining technique, which minimizes antibody consumption and allows for fast and convenient processing of samples for immunofluorescence microscopy of endogenous Tau in primary neurons. We also provide a protocol that enables cryopreservation of fixed cells for years without measurable loss of Tau signal. In sum, we provide reliable protocols enabling microscopy-based studies of Tau in primary murine neurons.
原代鼠神经元是研究神经元发育和神经退行性变过程中 Tau 的一种成熟工具。然而,培养原代神经元通常很耗时,需要进行多次喂养步骤、培养基更换、使用专有培养基补充剂和/或制备复杂的培养基。在这里,我们描述了一种相对廉价且简单的细胞培养方法,用于培养来自胚胎期(E13.5)小鼠的前脑神经元(i),该方法基于一种市售的神经元补充剂(NS21);(ii)一种从出生后(P0-P3)动物培养海马和皮质神经元的方案;(iii)用于神经元标志物和内源性 Tau 染色的基本固定和免疫荧光技术。我们展示了一种染色技术,该技术最大限度地减少了抗体的消耗,并允许快速方便地处理样品,以便对原代神经元中的内源性 Tau 进行免疫荧光显微镜检查。我们还提供了一种方案,可实现固定细胞的冷冻保存,多年后 Tau 信号无明显损失。总之,我们提供了可靠的方案,可用于在原代鼠神经元中进行基于显微镜的 Tau 研究。