Zeigler M, Bargal R, Suri V, Meidan B, Bach G
Department of Human Genetics, Hadassah University Hospital, Jerusalem, Israel.
Prenat Diagn. 1992 Dec;12(12):1037-42. doi: 10.1002/pd.1970121209.
Cultured amniotic fluid cells from two mucolipidosis type IV (MLIV)-affected fetuses demonstrated accumulation of phospholipids and gangliosides when compared with normal controls. Like cultured skin fibroblasts from MLIV patients, cultured amniotic cells from the affected fetuses accumulated primarily lyso phospholipids and this could be demonstrated by radioactive labelling with appropriate precursors, either inorganic phosphate or oleic acid. Furthermore, like cultured skin fibroblasts, there was significant retention of exogenously supplied GD1A ganglioside in the affected amniotic cells. This storage was previously demonstrated to be unique to MLIV and thus can be used at present as a specific procedure for prenatal diagnosis of MLIV.
与正常对照相比,来自两名患有IV型黏脂贮积症(MLIV)胎儿的羊水培养细胞显示出磷脂和神经节苷脂的积累。与MLIV患者的培养皮肤成纤维细胞一样,来自患病胎儿的羊水培养细胞主要积累溶血磷脂,这可以通过用适当的前体(无机磷酸盐或油酸)进行放射性标记来证明。此外,与培养的皮肤成纤维细胞一样,受影响的羊水中外源性供应的GD1A神经节苷脂有显著保留。这种储存以前被证明是MLIV所特有的,因此目前可以用作MLIV产前诊断的特定程序。