Hagiwara H
Institut für Toxikologie und Embryonal-Pharmakologie, Freie Universität Berlin, Federal Republic of Germany.
Histochemistry. 1992 Dec;98(5):305-9. doi: 10.1007/BF00270014.
The localization of proteoglycans in rat epiphyseal growth plate cartilage was investigated immunoelectron microscopically by the post-embedding method, using mouse monoclonal antibody (2-B-6) which specifically recognizes 4-sulphated chondroitin or dermatan sulphate after digestion of proteoglycans with chondroitinase ABC. Fixation with ruthenium hexamine trichloride (RHT) and embedding in LR White served to preserve chondrocytes in the expanded state and matrix proteoglycans were observed as a reticular network of filaments. Immunoelectron microscopy revealed gold labelling of the secondary antibodies for the demonstration of proteoglycans on these filamentous structures and in elements of the Golgi apparatus. Filaments associated with matrix vesicles were also labelled. After fixation in the presence of RHT, it was clearly demonstrated that cartilage matrix proteoglycans are retained approximately in their original spatial distribution and their antigenicity is well preserved.
采用包埋后法,通过免疫电子显微镜研究了大鼠骨骺生长板软骨中蛋白聚糖的定位。使用小鼠单克隆抗体(2-B-6),该抗体在软骨素酶ABC消化蛋白聚糖后能特异性识别4-硫酸软骨素或硫酸皮肤素。用三氯化六氨合钌(RHT)固定并包埋在LR White中,有助于将软骨细胞保持在扩张状态,基质蛋白聚糖表现为丝状网络。免疫电子显微镜显示,二抗的金标记用于在这些丝状结构和高尔基体成分上显示蛋白聚糖。与基质小泡相关的细丝也被标记。在RHT存在下固定后,清楚地表明软骨基质蛋白聚糖大致保留在其原始空间分布中,并且其抗原性得到了很好的保留。