Cole S, Humm S A
MRC Radiobiology Unit, Harwell, Oxfordshire, United Kingdom.
Stain Technol. 1987 Sep;62(5):285-90. doi: 10.3109/10520298709108012.
Adenosine polyphosphatase enzymes provide useful markers for epidermal Langerhans cells. Established adenosine polyphosphatase histochemical methods were refined and applied to demonstrate Langerhans cells in thin sheets of murine dorsal epidermis. The skin was supported during staining by attaching the keratinized surface to polyallyl diglycol carbonate "plastic" slides with cyanoacrylate adhesive and flattening it with pressure from a glass slide on the dermal surface. Optimal specific staining of dendritic Langerhans cells occurred after fixation of ethylenediaminetetraacetic acid-separated epidermal sheets in cacodylate buffered formaldehyde for 20 min and incubation, in the presence of magnesium and lead ions, with 9.36 X 10(-4) M adenosine diphosphate (ADP) for 45 min. Better definition of the cells was obtained with ADP as a substrate than with any concentration of adenosine triphosphate.
腺苷多磷酸酶为表皮朗格汉斯细胞提供了有用的标志物。对已有的腺苷多磷酸酶组织化学方法进行了改进,并应用于在小鼠背部表皮薄片中显示朗格汉斯细胞。在染色过程中,通过用氰基丙烯酸酯粘合剂将角质化表面附着到聚烯丙基二甘醇碳酸酯“塑料”载玻片上,并在真皮表面用载玻片施加压力使其平整,来支撑皮肤。在用乙二胺四乙酸分离的表皮薄片在二甲胂酸盐缓冲甲醛中固定20分钟,并在镁离子和铅离子存在的情况下,用9.36×10(-4)M二磷酸腺苷(ADP)孵育45分钟后,树突状朗格汉斯细胞出现了最佳的特异性染色。与任何浓度的三磷酸腺苷相比,以ADP为底物能更好地界定这些细胞。