Imaging Frontier Center, Organization for Research Advancement, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba, 278-8510, Japan.
Department of Biological Sciences, Graduate School of Science, Osaka University, Machikaneyama-cho 1-1, Toyonaka, Osaka, 560-0043, Japan.
Commun Biol. 2022 Jan 10;5(1):12. doi: 10.1038/s42003-021-02955-9.
Tissue clearing methods are increasingly essential for the microscopic observation of internal tissues of thick biological organs. We previously developed TOMEI, a clearing method for plant tissues; however, it could not entirely remove chlorophylls nor reduce the fluorescent signal of fluorescent proteins. Here, we developed an improved TOMEI method (iTOMEI) to overcome these limitations. First, a caprylyl sulfobetaine was determined to efficiently remove chlorophylls from Arabidopsis thaliana seedlings without GFP quenching. Next, a weak alkaline solution restored GFP fluorescence, which was mainly lost during fixation, and an iohexol solution with a high refractive index increased sample transparency. These procedures were integrated to form iTOMEI. iTOMEI enables the detection of much brighter fluorescence than previous methods in tissues of A. thaliana, Oryza sativa, and Marchantia polymorpha. Moreover, a mouse brain was also efficiently cleared by the iTOMEI-Brain method within 48 h, and strong fluorescent signals were detected in the cleared brain.
组织透明化方法对于观察厚生物器官内部组织的微观结构变得越来越重要。我们之前开发了一种用于植物组织的透明化方法(TOMEI),但它不能完全去除叶绿素,也不能降低荧光蛋白的荧光信号。在这里,我们开发了一种改进的 TOMEI 方法(iTOMEI)来克服这些限制。首先,确定了辛基磺基甜菜碱能够有效地从拟南芥幼苗中去除叶绿素,而不会猝灭 GFP。接下来,弱碱性溶液恢复了 GFP 荧光,该荧光在固定过程中主要丢失,高折射率的碘海醇溶液增加了样品的透明度。这些步骤被整合形成 iTOMEI。iTOMEI 使得在拟南芥、水稻和地钱的组织中能够检测到比以前的方法更亮的荧光。此外,通过 iTOMEI-Brain 方法,小鼠大脑在 48 小时内也能被有效地透明化,并且在透明化的大脑中检测到强烈的荧光信号。