NRF2/ARE pathway negatively regulates BACE1 expression and ameliorates cognitive deficits in mouse Alzheimer’s models

Gahee Bahn(Sungkyunkwan University), Jongsung Park(Johns Hopkins University), Ui Jeong Yun(Sungkyunkwan University), Yoon Jee Lee(Sungkyunkwan University), Yuri Choi(Sungkyunkwan University), Jin Su Park(Johns Hopkins University), Seung Hyun Baek(Sungkyunkwan University), Bo Youn Choi(Sungkyunkwan University), Yoon Suk Cho(Sungkyunkwan University), Hark Kyun Kim(Sungkyunkwan University), Jihoon Han(Sungkyunkwan University), Jae Hoon Sul(Sungkyunkwan University), Sang‐Ha Baik(National University of Singapore), Jinhwan Lim(University of California, Irvine), Nobunao Wakabayashi(University of Pittsburgh), Soo Han Bae(Yonsei University), Jeung‐Whan Han(Sungkyunkwan University), Thiruma V. Arumugam(National University of Singapore), Mark P. Mattson(National Institutes of Health), Dong‐Gyu Jo(Samsung (South Korea))
Proceedings of the National Academy of Sciences
June 4, 2019
Cited by 203Open Access
Full Text

Abstract

Significance Considering that Alzheimer’s disease (AD) is a chronic disease progressing over a long period of time, even a slight increase of BACE1 expression may have a profound effect on Aβ accumulation. We describe a previously unknown mechanism that negatively regulates BACE1 and BACE1-AS expression and demonstrate its pivotal role in the progression of Aβ and Tau pathologies and cognitive impairment in two mouse models of AD. Given the recent failures of the clinical trials using enzymatic inhibitors of BACE1, it is critical to explore alternative approaches such as down-regulating BACE1 and BACE1-AS transcription. Our finding that NRF2 negatively regulates BACE1 and BACE1-AS therefore suggests a potential for disease modification by NRF2-activating phytochemicals or synthetic small molecules in AD.


Related Papers

No related papers found

Powered by citation graph analysis