Laboratory of Molecular Cell Biology, College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, SK, Canada.
Neuroscience Research Cluster, University of Saskatchewan, Saskatoon, SK, Canada.
Cell Mol Neurobiol. 2018 Jan;38(1):317-328. doi: 10.1007/s10571-017-0529-6. Epub 2017 Aug 9.
Experimental models of multiple sclerosis (MS) have significantly advanced our understanding of pathophysiology and therapeutic interventions. Although in vivo rodent models are considered to most closely represent the complex cellular and molecular disease states of the human central nervous system (CNS), these can be costly to maintain and require long timelines. Organotypic slice cultures maintain the cytotypic organization observed in the intact CNS, yet provide many of the experimental advantages of in vitro cell culture models. Cerebellar organotypic cultures have proven useful for studying myelination and remyelination, but this model has only been established using early postnatal tissue. This young brain tissue allows for neuro development ex vivo to mimic the 'mature' CNS; however, there are many differences between postnatal and adult organotypic cultures. This may be particularly relevant to MS, as a major barrier to myelin regeneration is age. This paper describes a modified protocol to study demyelination and remyelination in adult cerebellar tissue, which has been used to demonstrate neuroprotection with omega-3 fatty acids. Thus, adult cerebellar organotypic cultures provide a novel ex vivo platform for screening potential therapies in myelin degeneration and repair.
实验性多发性硬化症 (MS) 模型极大地促进了我们对病理生理学和治疗干预的理解。尽管体内啮齿动物模型被认为最能代表人类中枢神经系统 (CNS) 的复杂细胞和分子疾病状态,但这些模型维持成本高,需要很长的时间。器官型切片培养保持了完整 CNS 中观察到的细胞表型组织,但提供了许多体外细胞培养模型的实验优势。小脑器官型培养已被证明可用于研究髓鞘形成和再髓鞘化,但这种模型仅使用早期产后组织建立。这种年轻的脑组织允许体外神经发育来模拟“成熟”的 CNS;然而,产后和成年器官型培养之间存在许多差异。这在多发性硬化症中可能特别重要,因为髓鞘再生的一个主要障碍是年龄。本文描述了一种改良的方案,用于研究成年小脑组织中的脱髓鞘和再髓鞘化,该方案已被用于证明 ω-3 脂肪酸的神经保护作用。因此,成年小脑器官型培养为筛选髓鞘退化和修复的潜在治疗方法提供了一个新的体外平台。