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储存疾病中人类脾窦碱性磷酸酶活性的诱导

Alkaline Phosphatase Activity Induction in Human Spleen Sinuses in Storage Diseases.

作者信息

Elleder M

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1979 Dec;32(1):89-92. doi: 10.1007/BF02889016.

DOI:10.1007/BF02889016
PMID:45156
Abstract

Human splenic sinuses were observed for the induction of alkaline phosphatase (AP) activity in mucopolysaccharidoses of type I and II, in GM1 gangliosidosis, and in Niemann-Pick's disease, type A. A substantially lower degree of activity was found in Sanfillipo's disease, type A, and in hemosiderin pigmentation of the sinuses. In a number of hematological affections and in control spleens AP activity could not be proved by histochemical means. From the formal pathogenetic view, enzyme activity induction is probably related to lysosomal deposition of the material stored.

摘要

观察人类脾窦,以研究I型和II型黏多糖贮积症、GM1神经节苷脂贮积症和A型尼曼-匹克病中碱性磷酸酶(AP)活性的诱导情况。在A型桑菲利波病和脾窦含铁血黄素沉着症中发现活性程度明显较低。在一些血液学疾病和对照脾脏中,无法通过组织化学方法证实AP活性。从形式病理学观点来看,酶活性诱导可能与所储存物质的溶酶体沉积有关。

相似文献

1
Alkaline Phosphatase Activity Induction in Human Spleen Sinuses in Storage Diseases.储存疾病中人类脾窦碱性磷酸酶活性的诱导
Virchows Arch B Cell Pathol Incl Mol Pathol. 1979 Dec;32(1):89-92. doi: 10.1007/BF02889016.
2
Mucopolysaccharidoses and mucolipidoses.黏多糖贮积症和黏脂贮积症。
J Clin Pathol Suppl (R Coll Pathol). 1974;8:64-93.
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[Mucolipidosis. biologic characteristics (author's transl)].
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[Characteristics of biochemical disorders in hereditary enzymopathies in humans and animals].[人类和动物遗传性酶病中的生化紊乱特征]
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Chromatofocusing of skin fibroblast sphingomyelinase: alterations in Niemann-Pick disease type C shared by GM1-gangliosidosis.皮肤成纤维细胞鞘磷脂酶的色谱聚焦法:GM1神经节苷脂贮积症所共有的尼曼-皮克病C型的改变。
Clin Chim Acta. 1983 May 30;130(2):155-61. doi: 10.1016/0009-8981(83)90112-2.
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The effect of glycosaminoglycans on the in vitro activity of human skin fibroblast glycosphingolipid beta-galactosidases and neuraminidases.糖胺聚糖对人皮肤成纤维细胞糖鞘脂β-半乳糖苷酶和神经氨酸酶体外活性的影响。
Clin Chim Acta. 1977 Oct 1;80(1):133-9. doi: 10.1016/0009-8981(77)90272-8.
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Lysosomal storage disorders. Diagnosis by ultrastructural examination of skin biopsy specimens.溶酶体贮积症。通过皮肤活检标本的超微结构检查进行诊断。
Arch Neurol. 1975 Sep;32(9):592-9. doi: 10.1001/archneur.1975.00490510048002.
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Niemann-Pick disease, Type C: evidence for the deficiency of an activating factor stimulating sphingomyelin and glucocerebroside degradation.尼曼-匹克病C型:刺激鞘磷脂和葡萄糖脑苷脂降解的激活因子缺乏的证据
Hoppe Seylers Z Physiol Chem. 1980 Oct;361(10):1489-502. doi: 10.1515/bchm2.1980.361.2.1489.
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The use of alpha-L-iduronidase activity determinations in leucocytes for the detection of Hurler and Scheie syndromes.利用白细胞中α-L-艾杜糖醛酸酶活性测定来检测胡尔勒综合征和谢伊综合征。
Clin Chim Acta. 1975 Apr 16;60(2):259-62. doi: 10.1016/0009-8981(75)90134-5.
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Sphingomyelinases and the genetic defects in Niemann-Pick disease.鞘磷脂酶与尼曼-匹克病的基因缺陷
Adv Exp Med Biol. 1976;68:367-78. doi: 10.1007/978-1-4684-7735-1_24.

引用本文的文献

1
Histochemical observations of induction and depression of enzyme activities in various pathological conditions: personal experience.各种病理状况下酶活性诱导与抑制的组织化学观察:个人经验
Histochem J. 1984 Apr;16(4):345-7. doi: 10.1007/BF01002845.
2
Deposition of lipopigment--a new feature of human splenic sinus endothelium (SSE). Ultrastructural and histochemical study.脂色素沉积——人类脾窦内皮细胞(SSE)的一个新特征。超微结构和组织化学研究。
Virchows Arch A Pathol Anat Histopathol. 1990;416(5):423-8. doi: 10.1007/BF01605148.