首页> 外文期刊>Journal of Neuroscience Methods >Localisation of connective tissue and inhibition of autofluorescence in the human optic nerve and nerve head using a modified picrosirius red technique and confocal microscopy.
【24h】

Localisation of connective tissue and inhibition of autofluorescence in the human optic nerve and nerve head using a modified picrosirius red technique and confocal microscopy.

机译:使用改良的picrosirius red技术和共聚焦显微镜在人的视神经和神经头中结缔组织的定位和自发荧光的抑制。

获取原文
获取原文并翻译 | 示例
           

摘要

The use of picrosirius red to localise connective tissue in thin tissue sections viewed by bright-field microscopy is well documented. Its use on thin tissue sections imaged by fluorescence confocal microscopy has also been reported. Here we describe modifications to published procedures that allow picrosirius red staining of thick 60-microm sections and their subsequent analysis by confocal microscopy. The use of phosphomolybdic acid pre-treatment was found to be essential for confocal analysis; in addition to preventing non-specific staining, it also quenched tissue autofluorescence. By incubating sections free-floating, pre-treating them with phosphomolybdic acid for 30 min and imaging them using an argon ion laser we were able to use confocal microscopy to image the entire depth of 60-microm human optic nerve and nerve head sections stained with picrosirius red. The application of this modified picrosirius red and confocal microscopy technique should be useful for analysing the three-dimensional structure of the optic nerve and other tissues with a similarly complex arrangement of connective tissue.
机译:充分记录了使用picrosirius红将结缔组织定位在薄组织切片中的明场显微镜观察。还已经报道了其在通过荧光共聚焦显微镜成像的薄组织切片上的用途。在这里,我们描述了对已公开程序的修改,该修改允许将皮克西里乌斯红染色为60微米厚的切片,并随后通过共聚焦显微镜对其进行了分析。已发现使用磷钼酸预处理对于共聚焦分析至关重要。除了防止非特异性染色外,它还能淬灭组织自发荧光。通过将自由漂浮的切片孵育,用磷钼酸对其进行预处理30分钟并使用氩离子激光对其进行成像,我们能够使用共聚焦显微镜对60微米的人类视神经和被染色的神经头部的整个深度进行成像picrosirius红色。这种改良的picrosirius红和共聚焦显微镜技术的应用对于分析视神经和其他具有类似复杂结缔组织排列的组织的三维结构应该是有用的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号