Suppr超能文献

细胞色素C氧化酶缺乏与门克斯卷发综合征中的神经元受累:免疫组织化学研究

Cytochrome C oxidase deficiency and neuronal involvement in Menkes' kinky hair disease: immunohistochemical study.

作者信息

Sparaco M, Hirano A, Hirano M, DiMauro S, Bonilla E

机构信息

Department of Neurology, College of Physicians and Surgeons of Columbia University, New York, NY 10032.

出版信息

Brain Pathol. 1993 Oct;3(4):349-54. doi: 10.1111/j.1750-3639.1993.tb00762.x.

Abstract

Antibodies against subunits II and IV of cytochrome c oxidase (COX) and against complex III of the respiratory chain were used to study the expression of these proteins in the cerebellum, spinal cord, and other regions of the central nervous system in an autoptic case of Menkes' kinky hair disease (MKHD). We found a reduced expression of COX subunits in all examined areas whereas staining for complex III appeared normal. Immunostaining was altered in morphologically well-preserved neurons, suggesting that COX deficiency may have a pathogenetic role in the neuronal degeneration of MKHD.

摘要

利用针对细胞色素c氧化酶(COX)亚基II和IV以及呼吸链复合体III的抗体,在一例门克斯卷发综合征(MKHD)的尸检病例中,研究这些蛋白质在小脑、脊髓和中枢神经系统其他区域的表达情况。我们发现,在所有检测区域中COX亚基的表达均降低,而复合体III的染色看起来正常。在形态保存良好的神经元中免疫染色发生改变,这表明COX缺乏可能在MKHD的神经元变性中起致病作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验