Kim Hanki, Kim Bum Jun, Koh Seungyon, Cho Hyo Jin, Jin Xuelian, Kim Byung Gon, Choi Jun Young
Department of Brain Science, Ajou University School of Medicine, Suwon 16499, Korea; Department of Biomedical Sciences, Ajou University Graduate School of Medicine, Suwon 16499, Korea.
Department of Brain Science, Ajou University School of Medicine, Suwon 16499, Korea; Department of Biomedical Sciences, Ajou University Graduate School of Medicine, Suwon 16499, Korea; Department of Neurology, Ajou University School of Medicine, Suwon 16499, Korea.
STAR Protoc. 2024 Dec 20;5(4):103327. doi: 10.1016/j.xpro.2024.103327. Epub 2024 Sep 28.
The generation of an oligodendrocyte primary culture model encompassing the diverse stages of the lineage is essential for the in vitro research of oligodendrocyte physiology and pathophysiology. Here, we provide a protocol for generating oligodendrocytes from the neonatal rodent brain. We describe steps for isolating oligodendrocyte progenitor cells (OPCs) through differential centrifugation, their subsequent expansion, passaging, and differentiation. For complete details on the use and execution of this protocol, please refer to Kim et al..
建立一个涵盖少突胶质细胞谱系不同阶段的原代培养模型,对于少突胶质细胞生理学和病理生理学的体外研究至关重要。在此,我们提供了一种从新生啮齿动物大脑中生成少突胶质细胞的方案。我们描述了通过差速离心分离少突胶质前体细胞(OPCs)的步骤,以及它们随后的扩增、传代和分化过程。有关该方案使用和执行的完整详细信息,请参考Kim等人的研究。