Sherriff F E, Joachim C L, Squier M V, Esiri M M
Department of Clinical Neurology (Neuropathology), University of Oxford, Radcliffe Infirmary, UK.
Neurosci Lett. 1995 Jul 14;194(1-2):37-40. doi: 10.1016/0304-3940(95)11718-c.
The nature of the inclusions in the human muscle disease inclusion-body myositis (IBM) has been the subject of debate. Parallels with Alzheimer's disease have been drawn after these inclusions were found to be ubiquitinated, and immunoreactive with antibodies to beta-amyloid (A beta) and certain amyloid-associated proteins. We have used a battery of antibodies against A beta and associated proteins to immunostain muscle biopsies from patients with IBM. Although the inclusions are ubiquitinated, we could not show immunoreactivity for A beta or the associated proteins investigated. We did, however, find that the ubiquitinated inclusions colocalised with the lysosomal marker, cathepsin D.
人类肌肉疾病——包涵体肌炎(IBM)中包涵体的性质一直是争论的焦点。在发现这些包涵体被泛素化,并与β-淀粉样蛋白(Aβ)及某些淀粉样蛋白相关蛋白的抗体发生免疫反应后,人们将其与阿尔茨海默病进行了类比。我们使用了一系列针对Aβ及相关蛋白的抗体,对IBM患者的肌肉活检样本进行免疫染色。尽管这些包涵体被泛素化,但我们并未发现其对所研究的Aβ或相关蛋白具有免疫反应性。不过,我们确实发现泛素化的包涵体与溶酶体标记物组织蛋白酶D共定位。