Frederik P M, Fortuin J J, Klepper D, Galjaard H
Histochem J. 1977 Jan;9(1):89-96. doi: 10.1007/BF01007011.
A method is described for localizing acid mucopolysaccharides autoradiographically in cultured cells. Normal fibroblasts and fibroblasts, from patients suffering from Mucopolysaccharidosis II disease (MPS II), were cultured for six days in the presence of 35SO4 and one day in unlabelled medium. The cultured cells were transferred to plastic film dish and, after settling, they were rapidly quenched, freeze-dried, fixed in osmium tetroxide vapour and embedded in Epon. Grain counting after autoradiography in 2 mum sections revealed a significant difference (P greater than 0.001) in 35SO4 incorporation in the perinuclear cytoplasm of MPS II cells and control cells grown under the same conditions. Autoradiography was also performed after mixing MPS II cells and control fibroblasts in a ratio 1:1-8 prior to freezing and the same ratio was found between labelled and unlabelled fibroblasts. These results demonstrate the feasibility of the present autoradiographic technique for the detection of the acid mucopolysaccharide storage at the single cell level.
本文描述了一种通过放射自显影法在培养细胞中定位酸性粘多糖的方法。将正常成纤维细胞和患有粘多糖贮积症II型(MPS II)患者的成纤维细胞在35SO4存在下培养6天,然后在无标记培养基中培养1天。将培养的细胞转移到塑料薄膜培养皿中,细胞沉降后,迅速淬灭、冷冻干燥,用四氧化锇蒸汽固定并包埋在环氧树脂中。对2μm切片进行放射自显影后的颗粒计数显示,在相同条件下生长的MPS II细胞和对照细胞的核周细胞质中35SO4掺入量存在显著差异(P>0.001)。在冷冻前将MPS II细胞和对照成纤维细胞按1:1 - 8的比例混合后也进行了放射自显影,标记和未标记的成纤维细胞之间也发现了相同的比例。这些结果证明了当前放射自显影技术在单细胞水平检测酸性粘多糖贮积的可行性。