Dreyfus J C, Belon J P, Gautron S, Lenoir G, Poenaru L
Biochem Biophys Res Commun. 1984 Mar 30;119(3):841-9. doi: 10.1016/0006-291x(84)90850-7.
The activity of seven lysosomal enzymes was determined in 25 lymphoblastoid cell lines. These lines included normal controls transformed with Epstein-Barr virus, Burkitt's lymphomas and other lymphomas with or without EBV genome. Four lines were deficient in total beta-hexosaminidase activity. The deficiency was as severe as that of the variant O (Sandhoff's disease) of clinical beta-hexosaminidase deficiency. The electrophoretic pattern was also similar to that observed in Sandhoff's disease. The possible mechanisms explaining the high frequency of beta-hexosaminidase deficiency in lymphoblastoid cell lines are discussed.
在25个淋巴母细胞系中测定了7种溶酶体酶的活性。这些细胞系包括用爱泼斯坦-巴尔病毒转化的正常对照、伯基特淋巴瘤以及其他有无EBV基因组的淋巴瘤。有4个细胞系的总β-己糖胺酶活性缺乏。这种缺乏的严重程度与临床β-己糖胺酶缺乏的O型变异体(桑德霍夫病)相当。电泳图谱也与在桑德霍夫病中观察到的相似。本文讨论了解释淋巴母细胞系中β-己糖胺酶缺乏高频率出现的可能机制。