外源性淀粉样蛋白纤维可导致神经退行性疾病蛋白的显著上调。

IF 4.1 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xihua Liu, Wenzhe Jia, Yapeng Fang, Yiping Cao
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引用次数: 0

摘要

阿尔茨海默病和帕金森病等神经退行性疾病与淀粉样纤维的形成有关。在家族性病例中,突变的致病基因通过淀粉样蛋白的过度表达或错误折叠,加剧了疾病的发展。此外,相当多的淀粉样变性病例是由外部因素引起的,但其起源和机制尚未完全明了。在这里,我们发现鸡蛋和牛奶蛋白产生的淀粉样纤维除了对肠道细胞有营养作用外,还能选择性地降低神经细胞和胰岛细胞的活力。相比之下,大豆蛋白淀粉样纤维对上述细胞缺乏细胞毒性。事实证明,这种蛋白质来源和细胞类型依赖性细胞毒性与淀粉样蛋白生成蛋白的显著上调有关。向小鼠静脉注射β-乳球蛋白纤维也证实了这一发现,小鼠体内的淀粉样β1-42(Aβ1-42)和胰岛淀粉样多肽明显上调。因此,这项研究有助于深入了解外源性淀粉样蛋白纤维对健康的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exogenous Amyloid Fibrils Can Cause Significant Upregulation of Neurodegenerative Disease Proteins.

Neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease, are associated with the formation of amyloid fibrils. In familial cases, the mutant causative genes accentuate disease progression through overexpression or misfolding of amyloidogenic proteins. Besides, considerable amyloidosis cases arise from external factors, but their origin and mechanisms are not yet fully understood. Herein, we found that amyloid fibrils generated from egg and milk proteins, in addition to their nutritional effects to intestinal cells, can selectively reduce the viability of nervous cells as well as pancreatic islet cells. In contrast, soy protein amyloid fibrils lacked cytotoxicity to the aforementioned cells. This protein source and cell type-dependent cytotoxicity are demonstrated to be associated with the significant upregulation of amyloidogenic proteins. The finding was also confirmed by the vein injection of beta-lactoglobulin fibrils to mice, exhibiting the pronounced upregulations of amyloid beta1-42 (Aβ1-42) and islet amyloid polypeptide in vivo. The study therefore provides insight into the health implications of exogenous amyloid fibrils.

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来源期刊
ACS Chemical Neuroscience
ACS Chemical Neuroscience BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
9.20
自引率
4.00%
发文量
323
审稿时长
1 months
期刊介绍: ACS Chemical Neuroscience publishes high-quality research articles and reviews that showcase chemical, quantitative biological, biophysical and bioengineering approaches to the understanding of the nervous system and to the development of new treatments for neurological disorders. Research in the journal focuses on aspects of chemical neurobiology and bio-neurochemistry such as the following: Neurotransmitters and receptors Neuropharmaceuticals and therapeutics Neural development—Plasticity, and degeneration Chemical, physical, and computational methods in neuroscience Neuronal diseases—basis, detection, and treatment Mechanism of aging, learning, memory and behavior Pain and sensory processing Neurotoxins Neuroscience-inspired bioengineering Development of methods in chemical neurobiology Neuroimaging agents and technologies Animal models for central nervous system diseases Behavioral research
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