Abstract
Sqstm1/p62 functions in the non-canonical activation of nuclear factor (erythroid-derived 2)-like 2 (Nrf2). However, its physiological relevance is not certain. Here, we show that p62 -/- mice exhibited an accelerated presentation of ageing phenotypes, and tissues from these mice created a pro-oxidative environment owing to compromised mitochondrial electron transport. Accordingly, mitochondrial function rapidly declined with age in p62 -/- mice. In addition, p62 enhanced basal Nrf2 activity, conferring a higher steady-state expression of NAD(P)H dehydrogenase, quinone 1 (Nqo1) to maintain mitochondrial membrane potential and, thereby, restrict excess oxidant generation. Together, the p62-Nrf2-Nqo1 cascade functions to assure mammalian longevity by stabilizing mitochondrial integrity.
Original language | English (US) |
---|---|
Pages (from-to) | 150-156 |
Number of pages | 7 |
Journal | EMBO Reports |
Volume | 13 |
Issue number | 2 |
DOIs | |
State | Published - Jan 2012 |
Keywords
- mammalian longevity
- mitochondria
- nqo1
- nrf2
- p62
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Genetics