Laboratory of Frontier Science, Tokyo Metropolitan Institute of Medical Science, Bunkyo-ku, Tokyo 113-8613, Japan.
Nat Cell Biol. 2010 Mar;12(3):213-23. doi: 10.1038/ncb2021. Epub 2010 Feb 21.
Impaired selective turnover of p62 by autophagy causes severe liver injury accompanied by the formation of p62-positive inclusions and upregulation of detoxifying enzymes. These phenotypes correspond closely to the pathological conditions seen in human liver diseases, including alcoholic hepatitis and hepatocellular carcinoma. However, the molecular mechanisms and pathophysiological processes in these events are still unknown. Here we report the identification of a novel regulatory mechanism by p62 of the transcription factor Nrf2, whose target genes include antioxidant proteins and detoxification enzymes. p62 interacts with the Nrf2-binding site on Keap1, a component of Cullin-3-type ubiquitin ligase for Nrf2. Thus, an overproduction of p62 or a deficiency in autophagy competes with the interaction between Nrf2 and Keap1, resulting in stabilization of Nrf2 and transcriptional activation of Nrf2 target genes. Our findings indicate that the pathological process associated with p62 accumulation results in hyperactivation of Nrf2 and delineates unexpected roles of selective autophagy in controlling the transcription of cellular defence enzyme genes.
自噬作用对 p62 的选择性降解功能受损会导致严重的肝损伤,同时伴有 p62 阳性包涵体的形成和解毒酶的上调。这些表型与人类肝脏疾病(包括酒精性肝炎和肝细胞癌)的病理状况非常吻合。然而,这些事件中的分子机制和病理生理过程仍不清楚。在这里,我们报告了 p62 对转录因子 Nrf2 的一种新的调节机制的鉴定,其靶基因包括抗氧化蛋白和解毒酶。p62 与 Keap1 的 Nrf2 结合位点相互作用,Keap1 是 Cullin-3 型泛素连接酶的一个组成部分,用于 Nrf2。因此,p62 的过度产生或自噬的缺乏与 Nrf2 和 Keap1 之间的相互作用竞争,导致 Nrf2 的稳定和 Nrf2 靶基因的转录激活。我们的研究结果表明,与 p62 积累相关的病理过程导致 Nrf2 的过度激活,并描绘了选择性自噬在控制细胞防御酶基因转录中的意外作用。