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Rapid increase in transparency of biological organs by matching refractive index of medium to cell membrane using phosphoric acid

机译:通过使用磷酸使培养基的折射率与细胞膜相匹配,可以快速提高生物器官的透明度

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Tissue clearing is a fundamental challenge in biology and medicine to achieve high-resolution optical imaging of tissues deep inside intact organs. The clearing methods reported up to now require long incubation times or physical/electrical pressure to achieve tissue clearing, which is done by matching the refractive indices of the whole sample and medium to that of the lipid layer. Here we show that phosphoric acid increases the refractive index of the medium and can increase the transparency of formalin-fixed tissue samples rapidly. While phosphoric acid (8.5–14.2 M) suppresses bright signals on the boundary of cells in their phase-contrast images, it does not damage the morphology of the phospholipid cell membrane. Immersion of fixed tissues of mice in phosphoric acid solutions (8.5–14.2 M) increased their transparency within 60 min in the case of 3 mm-thick fixed tissue specimens. Although further investigations are needed to apply this protocol to three-dimensional fluorescence imaging or immunohistochemistry, the protocol presented herein may contribute to developing better and faster soaking methods for tissue clearing than previously reported protocols.
机译:组织清除是生物学和医学领域中实现完整器官深处组织的高分辨率光学成像的一项基本挑战。迄今为止报道的清除方法需要较长的孵育时间或物理/电压力才能实现组织清除,这是通过使整个样品和介质的折射率与脂质层的折射率匹配来完成的。在这里,我们表明磷酸可以增加培养基的折射率,并可以迅速增加福尔马林固定的组织样品的透明度。尽管磷酸(8.5–14.2 M)在其相衬图像中抑制了细胞边界上的亮信号,但它不会破坏磷脂细胞膜的形态。对于厚度为3 mm的固定组织标本,将小鼠的固定组织浸入磷酸溶液(8.5–14.2 M)中可在60分钟内增加其透明度。尽管需要进一步研究以将该方案应用于三维荧光成像或免疫组织化学,但与先前报道的方案相比,本文介绍的方案可能有助于开发更好,更快的组织清除浸泡方法。

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