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I型细胞病(粘脂贮积症II型)。一例尸检病例的病理和生化研究。

I-cell disease (mucolipidosis 11). Pathological and biochemical studies of an autopsy case.

作者信息

Nagashima K, Sakakibara K, Endo H, Konishi Y, Nakamura N, Suzuki Y, Abe T

出版信息

Acta Pathol Jpn. 1977 Mar;27(2):251-64.

PMID:193352
Abstract

An autopsy case of I-cell disease was examined by histological, histochemical, ultrastructural and biochemical methods. Cultured fibroblasts contained numerous PAS- and oil-red O positive granules consistent with lysosomes. The beta-galactosidase activity was specifically low in liver of the patient. The fiboblast-like cells including the cardiac valves, periosteum and stromal cells of the organs were closely similar to those found in mucopolysaccharidoses histochemically as well as ultrastructurally. Lipid-like materials were observed massively in the myocardium and in the neurons of spinal ganglia, and from these organs excessive amount of ceramide tri-hexosides (CTH) was extracted. In a few hepatocytes the dense membrane-bound bodies suggestive of lipids were found by electron microscopy. Swollen glomerular epithelium contained strongly colloidal-iron positive material, but the amount of mucopolysaccharides in kidney was not elevated. In this paper, the relationship among the morphology, the material stored and the enzymes was discussed.

摘要

通过组织学、组织化学、超微结构和生物化学方法对1例I细胞病尸检病例进行了检查。培养的成纤维细胞含有大量与溶酶体一致的PAS和油红O阳性颗粒。患者肝脏中的β-半乳糖苷酶活性特别低。包括心脏瓣膜、骨膜和器官基质细胞在内的成纤维细胞样细胞在组织化学和超微结构上与黏多糖贮积症中发现的细胞非常相似。在心肌和脊髓神经节神经元中大量观察到类脂物质,并且从这些器官中提取了过量的神经酰胺三己糖苷(CTH)。通过电子显微镜在少数肝细胞中发现了提示脂质的致密膜结合体。肿胀的肾小球上皮含有强胶体铁阳性物质,但肾脏中黏多糖的量没有升高。本文讨论了形态、储存物质和酶之间的关系。

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