p62-Nrf2-p62 Mitophagy Regulatory Loop as a Target for Preventive Therapy of Neurodegenerative Diseases

Brain Sciences

IrinaS. Sadovnikova¹  ArtemP. Gureev¹  VasilyN. Popov¹  AnatolyA. Starkov²  NataliaN. Starkov³ 

[1] Department of Genetics, Cytology and Bioengineering, Voronezh State University, 394018 Voronezh, Russia;Neuroscience Department, Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY 10065, USA;Science Department, SUNY Maritime College, New York, NY 10465, USA;

关键词: mitochondria;    Nrf2;    p62;    mitophagy;    regulatory loop;    neurodegenerative disease;   

DOI  :  10.3390/brainsci10110847

来源: DOAJ

【 摘 要 】

Turnover of the mitochondrial pool due to coordinated processes of mitochondrial biogenesis and mitophagy is an important process in maintaining mitochondrial stability. An important role in this process is played by the Nrf2/ARE signaling pathway, which is involved in the regulation of the expression of genes responsible for oxidative stress protection, regulation of mitochondrial biogenesis, and mitophagy. The p62 protein is a multifunctional cytoplasmic protein that functions as a selective mitophagy receptor for the degradation of ubiquitinated substrates. There is evidence that p62 can positively regulate Nrf2 by binding to its negative regulator, Keap1. However, there is also strong evidence that Nrf2 up-regulates p62 expression. Thereby, a regulatory loop is formed between two important signaling pathways, which may be an important target for drugs aimed at treating neurodegeneration. Constitutive activation of p62 in parallel with Nrf2 would most likely result in the activation of mTORC1-mediated signaling pathways that are associated with the development of malignant neoplasms. The purpose of this review is to describe the p62-Nrf2-p62 regulatory loop and to evaluate its role in the regulation of mitophagy under various physiological conditions.

【 授权许可】

Unknown