Ozarkar Siddhi S, Patel Ridthi K R, Vulli Tasmai, Friar Carlee A, Burette Alain C, Philpot Benjamin D
Neuroscience Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Front Neuroanat. 2025 Mar 6;19:1535745. doi: 10.3389/fnana.2025.1535745. eCollection 2025.
Healthy brain development hinges on proper myelination, with disruption contributing to a wide array of neurological disorders. Immunohistochemical analysis of myelin basic protein (MBP) is a fundamental technique for investigating myelination and related disorders. However, despite decades of MBP research, detailed accounts of normal MBP progression in the developing mouse brain have been lacking. This study aims to address this gap by providing a detailed spatiotemporal account of MBP distribution across 13 developmental ages from postnatal day 2 to 60. We used an optimized immunohistochemistry protocol to overcome the challenges of myelin's unique lipid-rich composition, enabling more consistent staining across diverse brain structures and developmental stages, offering a robust baseline for typical myelination patterns, and enabling comparisons with pathological models. To support and potentially accelerate research into myelination disorders, we have made >1,400 high-resolution micrographs accessible online under the Creative Commons license.
健康的大脑发育取决于适当的髓鞘形成,髓鞘形成中断会导致多种神经系统疾病。髓鞘碱性蛋白(MBP)的免疫组织化学分析是研究髓鞘形成及相关疾病的一项基本技术。然而,尽管对MBP进行了数十年的研究,但仍缺乏关于发育中小鼠大脑中正常MBP进程的详细描述。本研究旨在通过提供从出生后第2天到60天的13个发育阶段MBP分布的详细时空描述来填补这一空白。我们使用了优化的免疫组织化学方案来克服髓鞘独特的富含脂质成分带来的挑战,从而在不同的脑结构和发育阶段实现更一致的染色,为典型的髓鞘形成模式提供了坚实的基线,并能够与病理模型进行比较。为了支持并可能加速对髓鞘形成障碍的研究,我们已根据知识共享许可在网上提供了1400多张高分辨率显微照片。