Rao J K, Letada P, Haverstick D M, Herman M M, Savory J
Department of Pathology, University of Virginia Health Sciences Center, Charlottesville 22908, USA.
Ann Clin Lab Sci. 1998 May-Jun;28(3):131-7.
The in situ detection of cells undergoing apoptosis is increasingly important in the analysis of injury and degeneration in the central nervous system. Limited information is presently available on the quantification of apoptosis in paraffin-embedded brain tissue sections, a technique which would be most useful in the evaluation of archival tissue for diagnostic and experimental purposes. In this report, optimized conditions for tissue digestion and permeabilization using Proteinase K and Triton X and a quantification method for apoptosis detection are described using brain sections from aluminum maltolate-treated aged and young rabbits as compared to untreated matched controls. This method provides optimal staining of apoptotic cells without the problem of tissue destruction, and should prove useful in evaluating the process of apoptosis in neurodegenerative disorders.
在中枢神经系统损伤与退变分析中,原位检测凋亡细胞愈发重要。目前关于石蜡包埋脑组织切片中凋亡定量的信息有限,而该技术在诊断和实验目的的存档组织评估中最为有用。在本报告中,描述了使用蛋白酶K和曲拉通X进行组织消化和通透化的优化条件,以及与未处理的匹配对照相比,使用麦芽酚铝处理的老年和幼年兔子的脑切片进行凋亡检测的定量方法。该方法能为凋亡细胞提供最佳染色,且不存在组织破坏问题,应可用于评估神经退行性疾病中的凋亡过程。