Limited expression of Nrf2 in neurons across the central nervous system

被引:7
作者
Levings, Daniel C. [1 ]
Pathak, Salil Saurav [1 ]
Yang, Yi-Mei [1 ,2 ]
Slattery, Matthew [1 ,3 ]
机构
[1] Univ Minnesota, Dept Biomed Sci, Med Sch, Duluth, MN 55812 USA
[2] Univ Minnesota, Dept Neurosci, Med Sch, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Med Sch, 1035 Univ Dr, SMed 255 Duluth, Minneapolis, MN 55812 USA
关键词
NRF2; Neuron; Brain; Reactive oxygen species; Gene expression; Single cell RNA-seq; ANTIOXIDANT RESPONSE ELEMENT; TRANSCRIPTION FACTOR NRF2; OXIDATIVE STRESS; COORDINATE REGULATION; ACTIVATION; PATHWAY; KEAP1; GLIA; INDUCTION; CULTURES;
D O I
10.1016/j.redox.2023.102830
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nrf2, encoded by the gene Nfe2l2, is a broadly expressed transcription factor that regulates gene expression in response to reactive oxygen species (ROS) and oxidative stress. It is commonly referred to as a ubiquitous pathway, but this generalization overlooks work indicating that Nrf2 is essentially unexpressed in some neuronal populations. To explore whether this pattern extends throughout the central nervous system (CNS), we quan-tified Nfe2l2 expression and chromatin accessibility at the Nfe2l2 locus across multiple single cell datasets. In both the mouse and human CNS, Nfe2l2 was repressed in almost all mature neurons, but highly expressed in non-neuronal support cells, and this pattern was robust across multiple human CNS diseases. A subset of key Nrf2 target genes, like Slc7a11, also remained low in neurons. Thus, these data suggest that while most cells express Nfe2l2, with activity determined by ROS levels, neurons actively avoid Nrf2 activity by keeping Nfe2l2 expression low.
引用
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页数:8
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