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尼曼-匹克病患者培养的皮肤成纤维细胞中的鞘磷脂酶活性。

Sphingomyelinase activities in cultured skin fibroblasts from patients with Niemann-Pick Disease.

作者信息

Minami R, Matsuura Y, Nakamura F, Kudoh T, Sogawa H, Oyanagi K, Sukegawa K, Orii T, Maruyama K, Nakao T

出版信息

Hum Genet. 1979 Mar 12;47(2):159-67. doi: 10.1007/BF00273198.

Abstract

Sphingomyelinase activity in cultured skin fibroblasts from a fetus affected with infantile-type Niemann-Pick disease was 0.5% of control activity; the activities in cells from two patients with adult-type disease (Cases 2 and 3) were 5.0% and 59.0%. Sphingomyelinase activiy was separated into three peaks (I-III) by isoelectric focusing. The isoelectric points were 4.5, 4.9, and 5.2 for peaks I, II, and III, respectively. The three peaks in the Case 2 cells were drastically reduced; only a very small peak could be distinguished (pI of 4.7). On the other hand, three peaks were observed in the Case 3 cells. Peak I had a pI of 4.4, peak II a pI of 4.7, and peak III a pI of 5.2. Peak I was found at near normal level, but both peaks II and III were markedly reduced. Sphingomyelinase in the peak I fraction obtained from isoelectric focusing in Case 3 cells was found to have the same Km value as that in control cells.

摘要

患有婴儿型尼曼-匹克病的胎儿培养皮肤成纤维细胞中的鞘磷脂酶活性为对照活性的0.5%;两名成年型疾病患者(病例2和病例3)细胞中的活性分别为5.0%和59.0%。通过等电聚焦将鞘磷脂酶活性分离为三个峰(I-III)。峰I、II和III的等电点分别为4.5、4.9和5.2。病例2细胞中的三个峰大幅降低;只能分辨出一个非常小的峰(pI为4.7)。另一方面,在病例3细胞中观察到三个峰。峰I的pI为4.4,峰II的pI为4.7,峰III的pI为5.2。峰I处于接近正常的水平,但峰II和峰III均明显降低。发现从病例3细胞的等电聚焦获得的峰I部分中的鞘磷脂酶具有与对照细胞中相同的Km值。

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