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EBP1通过调节γ-分泌酶增强β淀粉样蛋白病理。

EBP1 potentiates amyloid β pathology by regulating γ-secretase.

作者信息

Kim Byeong-Seong, Hwang Inwoo, Ko Hyo Rim, Kim Young Kwan, Kim Hee Jin, Seo Sang Won, Choi Yujung, Lim Sungsu, Kim Yun Kyung, Nie Shuke, Ye Keqiang, Park Jong-Chan, Lee Yunjong, Jo Dong-Gyu, Lee Seung Eun, Kim Daesik, Cho Sung-Woo, Ahn Jee-Yin

机构信息

Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon, Korea.

Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Korea.

出版信息

Nat Aging. 2025 Mar;5(3):486-503. doi: 10.1038/s43587-024-00790-1. Epub 2025 Jan 8.

Abstract

The abnormal deposition of amyloid β (Aβ), produced by proteolytic cleavage events of amyloid precursor protein involving the protease γ-secretase and subsequent polymerization into amyloid plaques, plays a key role in the neuropathology of Alzheimer's disease (AD). Here we show that ErbB3 binding protein 1 (EBP1)/proliferation-associated 2G4 (PA2G4) interacts with presenilin, a catalytic subunit of γ-secretase, inhibiting Aβ production. Mice lacking forebrain Ebp1/Pa2g4 recapitulate the representative phenotypes of late-onset sporadic AD, displaying an age-dependent increase in Aβ deposition, amyloid plaques and cognitive dysfunction. In postmortem brains of patients with AD and 5x-FAD mice, we found that EBP1 is proteolytically cleaved by asparagine endopeptidase at N84 and N204 residues, compromising its inhibitory effect on γ-secretase, increasing Aβ aggregation and neurodegeneration. Accordingly, injection of AAV2-Ebp1 wild-type or an asparagine endopeptidase-uncleavable mutant into the brains of 5x-FAD mice decreased Aβ generation and alleviated the behavioral impairments. Thus, our study suggests that EBP1 acts as an inhibitor of γ-secretase on amyloid precursor protein cleavage and preservation of functional EBP1 could be a therapeutic strategy for AD.

摘要

淀粉样前体蛋白经蛋白酶γ-分泌酶的蛋白水解切割事件产生的β淀粉样蛋白(Aβ)异常沉积,并随后聚合成淀粉样斑块,在阿尔茨海默病(AD)的神经病理学中起关键作用。在此我们表明,ErbB3结合蛋白1(EBP1)/增殖相关2G4(PA2G4)与早老素(γ-分泌酶的催化亚基)相互作用,抑制Aβ生成。缺乏前脑Ebp1/Pa2g4的小鼠重现了晚发性散发性AD的典型表型,表现出Aβ沉积、淀粉样斑块和认知功能障碍的年龄依赖性增加。在AD患者和5x-FAD小鼠的死后大脑中,我们发现EBP1在N84和N204残基处被天冬酰胺内肽酶蛋白水解切割,损害了其对γ-分泌酶的抑制作用,增加了Aβ聚集和神经退行性变。因此,向5x-FAD小鼠脑内注射AAV2-Ebp1野生型或天冬酰胺内肽酶不可切割的突变体可减少Aβ生成并减轻行为障碍。因此,我们的研究表明EBP1作为γ-分泌酶对淀粉样前体蛋白切割的抑制剂,保留功能性EBP1可能是AD的一种治疗策略。

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