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二甲基亚砜对正常及A、B、C型尼曼-匹克病成纤维细胞中鞘磷脂酶活性的影响。

Effects of dimethylsulfoxide on sphingomyelinase activities in normal and Niemann-Pick type A, B and C fibroblasts.

作者信息

Sato M, Yoshida Y, Sakuragawa N, Arima M

机构信息

Division of Mental Retardation and Birth Defect Research, National Institute of Neural Science, Tokyo, Japan.

出版信息

Biochim Biophys Acta. 1988 Sep 2;962(1):59-65.

PMID:2843241
Abstract

The effects of dimethylsulfoxide (DMSO) on sphingomyelinase activity measured at pH range 3.5-8.0 were examined in normal and Niemann-Pick disease type A, B and C fibroblasts culture. In normal cells, a minor activity was observed at pH 7.5, which was 3- to 4-fold lower than a major one at pH 5.0. Both activities at pH 5.0 and 7.5 were Mg2+-independent and localized to lysosomes. Niemann-Pick type C cells had 30-50% residual sphingomyelinase activity at both pH 5.0 and 7.5, as compared to normal control cells, whereas type A and B cells exhibited virtually no activity over the entire pH range examined. Treatment with 2% DMSO caused a marked increase in sphingomyelinase activities at pH 5.0 and 7.5 in normal and Niemann-Pick disease type C cells, while in type A and B cells, both activities remained virtually unchanged after DMSO treatment. The increase in sphingomyelinase activity at pH 5.0 induced in normal cells by DMSO resulted in an increase in the Vmax without a substantial change in the Km and was inhibited by the simultaneous addition of 10 micrograms/ml of cycloheximide. By comparison, a less than 2-fold increase in other lysosomal hydrolase activities was observed after DMSO treatment in all cell lines examined.

摘要

在正常以及A型、B型和C型尼曼-匹克病成纤维细胞培养物中,研究了二甲基亚砜(DMSO)对在pH范围3.5 - 8.0测定的鞘磷脂酶活性的影响。在正常细胞中,在pH 7.5观察到较小的活性,其比在pH 5.0时的主要活性低3至4倍。pH 5.0和7.5时的这两种活性均不依赖于Mg2 +,且定位于溶酶体。与正常对照细胞相比,C型尼曼-匹克病细胞在pH 5.0和7.5时均具有30 - 50%的残余鞘磷脂酶活性,而A型和B型细胞在整个检测的pH范围内几乎没有活性。用2% DMSO处理导致正常细胞和C型尼曼-匹克病细胞在pH 5.0和7.5时鞘磷脂酶活性显著增加,而在A型和B型细胞中,DMSO处理后这两种活性几乎保持不变。DMSO在正常细胞中诱导的pH 5.0时鞘磷脂酶活性增加导致Vmax增加,而Km没有实质性变化,并且同时添加10微克/毫升放线菌酮可抑制该增加。相比之下,在所检测的所有细胞系中,DMSO处理后其他溶酶体水解酶活性的增加不到2倍。

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