Slaoui Mohamed, Bauchet Anne-Laure, Fiette Laurence
Preclinical Safety, Sanofi R&D, 13, Quai Jules Guesde, BP14, 94403, Vitrysur-Seine, France.
Translational Medicine and Early Development, Biomarkers and Clinical Bioanalysis, Sanofi R&D, Vitry-sur-Seine, France.
Methods Mol Biol. 2017;1641:101-114. doi: 10.1007/978-1-4939-7172-5_4.
Histological procedures aim at providing good-quality sections that can be used for a light microscopic evaluation of tissue. These are applicable to identify either spontaneous or diseases-induced changes. Routinely, tissues are fixed with neutral formalin 10%, embedded in paraffin, and manually sectioned with a microtome to obtain 4-5 μm thick paraffin sections. Dewaxed sections are then stained with HE&S (hematoxylin-eosin and saffron) or can be used for other purposes (special stains, immunohistochemistry, in situ hybridization, etc.). During this processing, many steps and procedures are critical to ensure standard and interpretable sections. This chapter provides key recommendations to efficiently achieve this objective.
组织学程序旨在提供高质量的切片,可用于对组织进行光学显微镜评估。这些程序适用于识别自发或疾病诱导的变化。通常,组织用10%的中性福尔马林固定,包埋在石蜡中,并用切片机手动切片以获得4-5微米厚的石蜡切片。脱蜡后的切片然后用苏木精-伊红和番红花染色(HE&S),或者可用于其他目的(特殊染色、免疫组织化学、原位杂交等)。在这个过程中,许多步骤和程序对于确保切片的标准性和可解释性至关重要。本章提供了有效实现这一目标的关键建议。