Steinke Hanno, Wiersbicki Dina, Speckert Marie-Lynn, Merkwitz Claudia, Wolfskämpf Thomas, Wolf Benjamin
Institute for Anatomy, Leipzig University, Liebigstr. 13, D-04103 Leipzig, Germany.
Institute for Anatomy, Leipzig University, Liebigstr. 13, D-04103 Leipzig, Germany.
Ann Anat. 2018 Mar;216:29-35. doi: 10.1016/j.aanat.2017.10.001. Epub 2017 Nov 13.
Since collagen rich fascial tissue is often very delicate and difficult to discern on native tissue slices, we have developed a method for staining full-body slices using the periodic acid-Schiff (PAS) reaction with subsequent plastination. Since the PAS reaction primarily stains carbohydrates, we could exploit the circumstance that different collagen types vary in carbohydrate content. Contrary to fasciae, tissues such as muscle, bone, nerves and blood vessels exhibit significantly less staining or remain unstained. We have validated the whole-body slice staining results in microscopic tissue slides which were stained with standard extracellular matrix stains such as Masson-Goldner trichrome stain and van-Gieson stain. Furthermore, we have performed immunofluorescence imaging to confirm the presence of collagen in the stained tissue. We achieved very good staining and plastination results and were able to clearly identify even very thin fascia in transversal body slices. This technique may prove useful in advancing our knowledge on the complex topography of fascial structures.
由于富含胶原蛋白的筋膜组织通常非常脆弱,在原生组织切片上难以辨别,我们开发了一种方法,即使用过碘酸-希夫(PAS)反应对全身切片进行染色,随后进行塑化处理。由于PAS反应主要对碳水化合物进行染色,我们可以利用不同类型胶原蛋白碳水化合物含量不同这一情况。与筋膜相反,肌肉、骨骼、神经和血管等组织染色明显较少或未染色。我们已在显微组织切片中验证了全身切片染色结果,这些切片用标准细胞外基质染色剂如马森-戈德纳三色染色法和范-吉森染色法进行了染色。此外,我们进行了免疫荧光成像,以确认染色组织中胶原蛋白的存在。我们获得了非常好的染色和塑化效果,并且能够在横向身体切片中清晰地识别出非常薄的筋膜。这项技术可能有助于增进我们对筋膜结构复杂形态的了解。