Activation of NRF2 ameliorates oxidative stress and cystogenesis in autosomal dominant polycystic kidney disease

Yi Lu(Tianjin Medical University), Yi Lu(Tianjin Medical University), Yongzhan Sun(Tianjin Medical University), Zhiheng Liu(Tianjin Medical University), Yumei Lu(Tianjin Medical University), Yumei Lu(Tianjin Medical University), Xu Zhu(Tianjin Medical University), Bingxue Lan(Tianjin Medical University), Zeyun Mi(Tianjin Medical University), Lin Dang(Tianjin Medical University), Na Li(Tianjin University of Science and Technology), Wenlei Zhan(Tianjin Medical University), Lu Tan(Tianjin University of Science and Technology), Jingbo Pi(Tianjin Medical University), Hui Xiong(Shandong Provincial Hospital), Lirong Zhang(Tianjin Medical University), Yupeng Chen(Tianjin Medical University)
Science Translational Medicine
July 29, 2020
Cited by 114

Abstract

further increased ROS generation and promoted cyst growth, whereas pharmacological induction of NRF2 reduced ROS production and slowed cystogenesis and disease progression. Mechanistically, pharmacological induction of NRF2 remodeled enhancer landscapes and activated NRF2-bound enhancer-associated genes in ADPKD cells. The activation domain of NRF2 formed phase-separated condensates with MEDIATOR complex subunit MED16 in vitro, and optimal Mediator recruitment to genomic loci depended on NRF2 in vivo. Together, these findings indicate that NRF2 remodels enhancer landscapes and activates its target genes through a phase separation mechanism and that activation of NRF2 represents a promising strategy for restoring redox homeostasis and combatting ADPKD.


Related Papers

No related papers found

Powered by citation graph analysis