Maeda H, Ishikawa H, Ohta S
Br J Dermatol. 1981 Sep;105(3):239-45. doi: 10.1111/j.1365-2133.1981.tb01281.x.
Using a new method devised by our laboratory, the ultrastructure of dermal glycosaminoglycan in an involved area of lichen myxoedematosus was examined. Although histochemical and biochemical studies have indicated simply an accumulated deposition of hyaluronic acid in the lesion, the glycosaminoglycan ultrastructure within it was distinctly different from that in normal skin. The glycosaminoglycan structure of normal skin was similar to the proteoglycan aggregate model described by Rosenberg (1975). As confirmed by the enzymatic digestion procedure, it represents the ultrastructure of hyaluronic acid bound to glycosaminoglycans such as dermatan sulphate or chondroitin sulphate. In contrast, hyaluronic acid filaments observed in lesions of lichen myxoedematosus contained no glycosaminoglycan subunits.
使用我们实验室设计的一种新方法,对黏液性水肿性苔藓受累区域的真皮糖胺聚糖超微结构进行了检查。尽管组织化学和生物化学研究仅表明病变中透明质酸有累积沉积,但其中的糖胺聚糖超微结构与正常皮肤明显不同。正常皮肤的糖胺聚糖结构类似于罗森伯格(1975年)描述的蛋白聚糖聚集模型。经酶消化程序证实,它代表了与硫酸皮肤素或硫酸软骨素等糖胺聚糖结合的透明质酸的超微结构。相比之下,在黏液性水肿性苔藓病变中观察到的透明质酸细丝不含糖胺聚糖亚基。