Department of Biomedicine, Musculoskeletal Research Group, University of Basel, Switzerland.
Histol Histopathol. 2013 Dec;28(12):1605-11. doi: 10.14670/HH-28.1605. Epub 2013 May 29.
Processing adult human trabecular bone to obtain tissue sections suitable for research or diagnostic purposes has always been challenging, particularly in the preparation of adult bone specimens for advanced immunohistochemistry applications. In contrast to the majority of soft tissues, decalcified bone samples perform poorly under standard paraffin embedding techniques and immunolabeling protocols fail frequently, due to the loss of protein antigenicity observed. We report on a new, PVA based infiltration method that avoids excessive heat exposure to tissue samples during embedding. The developed PVA based infiltration medium provides sufficient structural support to the heterogenic morphology and distinct architecture of subchondral trabecular bone and adjacent articular cartilage. Furthermore, the addition of bovine serum albumin (BSA) to this infiltration solution guaranteed safe attachment of cryosections to glass slides. The protocol allows the preparation of high quality sections of adult human trabecular bone tissues which can be used for both classical histochemical stains and for immunohistochemistry, since protein antigenicity is satisfactorily preserved.
处理成人松质骨以获得适合研究或诊断目的的组织切片一直具有挑战性,特别是在为高级免疫组织化学应用准备成人骨标本时。与大多数软组织不同,脱钙骨样本在标准石蜡包埋技术下表现不佳,并且由于观察到蛋白质抗原性丧失,免疫标记协议经常失败。我们报告了一种新的基于 PVA 的渗透方法,该方法在包埋过程中避免了组织样本过度受热。开发的基于 PVA 的渗透介质为软骨下松质骨和相邻关节软骨的异质形态和独特结构提供了足够的结构支撑。此外,将牛血清白蛋白 (BSA) 添加到该渗透溶液中可确保将冷冻切片安全地附着到载玻片上。该方案允许制备高质量的成人松质骨组织切片,这些切片可用于经典组织化学染色和免疫组织化学,因为蛋白质抗原性得到了令人满意的保留。