Department of Pathology and Laboratory Medicine, University of California, Irvine, D440 Medical Sciences 1, Irvine, CA 92697, USA.
Toxicol Appl Pharmacol. 2010 Apr 1;244(1):16-20. doi: 10.1016/j.taap.2009.07.034. Epub 2009 Aug 6.
Oxidative stress plays an important part in the pathogenesis of a variety of diseases. The ability to mount an efficient response against the continuous threat posed by exogenous and endogenous oxidants is essential for cellular homeostasis and survival. Oxidative stress activates transcription of a variety of antioxidant genes through cis-acting sequence known as antioxidant response element (ARE). Members of the Cap-N-Collar family of transcription factors, including Nrf1 and Nrf2, that bind ARE have been identified. Nrf1 and Nrf2 are expressed in a wide range of tissues and cell types, and both bind the ARE as heterodimers with small Maf proteins. Numerous studies indicate a pivotal role of Nrf2 in ARE function. Herein, we review data derived from cell-based studies and knockout mice in an attempt to define the role and regulation of Nrf1 in oxidative stress response and other functions.
氧化应激在多种疾病的发病机制中起着重要作用。机体抵御外源性和内源性氧化剂持续威胁的能力对于细胞内环境稳定和生存至关重要。氧化应激通过顺式作用序列(称为抗氧化反应元件,ARE)激活多种抗氧化基因的转录。已经鉴定出包括 Nrf1 和 Nrf2 在内的 Cap-N-Collar 家族转录因子成员,它们可以与 ARE 结合。Nrf1 和 Nrf2 在广泛的组织和细胞类型中表达,并作为与小 Maf 蛋白形成的异二聚体结合 ARE。大量研究表明 Nrf2 在 ARE 功能中起着关键作用。本文通过细胞水平的研究和敲除小鼠模型来综述数据,试图确定 Nrf1 在氧化应激反应和其他功能中的作用和调节机制。