University of Calgary, Hotchkiss Brain Institute, Calgary Cumming School of Medicine, Department of Clinical Neurosciences, 3330 Hospital Drive N.W. HRIC 1B37A, Calgary, AB, T2N 4N1, Canada.
J Neurosci Methods. 2021 Aug 1;360:109226. doi: 10.1016/j.jneumeth.2021.109226. Epub 2021 May 27.
Label-free methods for quantifying myelination can reduce expense, time, and variability in results when examining tissue white matter pathology.
We sought to determine whether the optical birefringent properties of myelin could be exploited to determine myelination status of white matter in tissue sections. Sections of forebrains of mice (normal, and treated with cuprizone to cause demyelination) were examined by birefringence using a birefringence imaging system (Thorlabs LCC7201), and results compared with sections stained using Luxol Fast Blue.
Quantitative birefringence analysis of myelin was not only reliable in detecting demyelination, but also showed abnormalities that preceded myelin loss in cuprizone-treated mice.
Subtle myelin pathology visible with electron microscopy but not with conventional histopathological staining was readily detected with birefringence microscopy.
Birefringence imaging provides a rapid, label-free method of analyzing the myelin content and nanostructural status in longitudinal white matter structures, being sensitive to subtle myelin changes that precede overt pathological damage.
用于量化髓鞘的无标记方法可以减少在检查组织白质病理学时的费用、时间和结果变异性。
我们试图确定髓鞘的光学双折射特性是否可以被利用来确定组织切片中白质的髓鞘状态。使用双折射成像系统(Thorlabs LCC7201)对正常和用铜蓝蛋白处理以引起脱髓鞘的小鼠大脑前脑切片进行双折射检查,并将结果与使用卢戈氏快速蓝染色的切片进行比较。
髓鞘的定量双折射分析不仅可靠地检测到脱髓鞘,而且还显示出在铜蓝蛋白处理的小鼠中髓鞘丢失之前存在的异常。
用电子显微镜可见但用常规组织病理学染色不可见的细微髓鞘病理学,用双折射显微镜很容易检测到。
双折射成像提供了一种快速、无标记的方法来分析纵向白质结构中的髓鞘含量和纳米结构状态,对先前明显病理损伤的细微髓鞘变化敏感。