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[致密性骨发育不全中软骨细胞的超微结构异常。它们与脂质代谢紊乱的关系]

[Ultrastructural abnormalities of the chondrocytes in pycnodysostosis. Their relation to a disorder of lipid metabolism].

作者信息

Stanescu R, Stanescu V, Maroteaux P

出版信息

Nouv Presse Med. 1975 Nov 1;4(37):2647-50.

PMID:172867
Abstract

The ultrastructural study of the growth cartilage of pycnodysostosis reveals the presence of abnormal inclusions in the majority of the chondrocytes. The inclusions are single membrane bound and contain granular material and lamellar irregularly interwoven structures which at very high magnification appear to be made up of dense parallel bands. These vacuoles displace adjacent structures and some of them appear to be closely related to the Golgi apparatus. In addition, appearances are sometimes seen which suggest the expulsion of the vacuoles into the cell capsules. The abnormal chondrocyte inclusions are visible by optic microscopy and stained with Nile blue on frozen section. Thus, histochemical and ultrastructural characteristics suggest a lipid (probably phospholipid) content. Many authors have already stressed the role of lipids in the process of calcification. The abnormalities described might bear some relation to the densification of the skeleton seen in pycnodysostosis.

摘要

致密性成骨不全症生长软骨的超微结构研究显示,大多数软骨细胞中存在异常包涵体。这些包涵体由单层膜包被,含有颗粒物质和层状不规则交织结构,在极高放大倍数下似乎由密集的平行带组成。这些空泡会挤压相邻结构,其中一些似乎与高尔基体密切相关。此外,有时会观察到一些现象,提示空泡被排出到细胞囊泡中。通过光学显微镜在冰冻切片上用尼罗蓝染色可观察到异常的软骨细胞包涵体。因此,组织化学和超微结构特征提示其含有脂质(可能是磷脂)。许多作者已经强调了脂质在钙化过程中的作用。所描述的这些异常可能与致密性成骨不全症中所见的骨骼致密化有一定关系。

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