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热休克蛋白在阿尔茨海默病中的表达。

Expression of heat shock proteins in Alzheimer's disease.

作者信息

Hamos J E, Oblas B, Pulaski-Salo D, Welch W J, Bole D G, Drachman D A

机构信息

Department of Neurology, University of Massachusetts Medical Center, Worcester 01655.

出版信息

Neurology. 1991 Mar;41(3):345-50. doi: 10.1212/wnl.41.3.345.

Abstract

In an investigation of heat shock proteins (HSPs) in the brains of Alzheimer's disease (AD) patients and cognitively intact control subjects, we found that 2 HSPs, termed "HSP72" and "GRP78," underwent major changes in expression in AD. HSP72, which was present at very low levels in control brains, increased dramatically in AD patients, and was localized exclusively in neuritic plaques and neurofibrillary tangles. We hypothesize that HSP72 is induced as an early response to the formation of abnormal proteins, perhaps targeting them for proteolysis. In contrast, GRP78 increased in AD only in neurons that remained cytologically normal, especially in the CA3 subfield of the hippocampus and the deep layers of the entorhinal cortex. The increased expression of GRP78 within successfully surviving neurons suggests that this protein may protect such cells from AD-specific damage.

摘要

在一项针对阿尔茨海默病(AD)患者大脑和认知功能正常的对照受试者大脑中热休克蛋白(HSPs)的研究中,我们发现两种名为“HSP72”和“GRP78”的热休克蛋白在AD患者大脑中的表达发生了重大变化。HSP72在对照大脑中含量极低,在AD患者大脑中急剧增加,并且仅定位于神经炎性斑块和神经原纤维缠结中。我们推测,HSP72是作为对异常蛋白质形成的早期反应而被诱导产生的,可能是将它们靶向进行蛋白水解。相比之下,GRP78仅在细胞学上仍保持正常的神经元中增加,尤其是在海马体的CA3亚区和内嗅皮质深层。成功存活的神经元内GRP78表达增加表明,这种蛋白质可能保护这些细胞免受AD特异性损伤。

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