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核因子-κB激活的氧化还原调节:细胞质与细胞核之间不同的氧化还原调节

Redox regulation of NF-kappaB activation: distinct redox regulation between the cytoplasm and the nucleus.

作者信息

Kabe Yasuaki, Ando Kozue, Hirao Satoshi, Yoshida Makoto, Handa Hiroshi

机构信息

Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.

出版信息

Antioxid Redox Signal. 2005 Mar-Apr;7(3-4):395-403. doi: 10.1089/ars.2005.7.395.

Abstract

Reduction/oxidation (redox) regulation mediates numerous cellular responses and contributes to several physiological diseases. The transcription factor nuclear factor kappaB (NF-kappaB) is known to be a redox-sensitive factor. NF-kappaB plays a central role in immune responses and inflammation, through regulation of the gene expression of a large number of cytokines and other immune response genes. NF-kappaB is trapped in the cytoplasm in stimulated cells and translocates into the nucleus in response to several stimuli, including oxidative stress. Reactive oxygen species enhance the signal transduction pathways for NF-kappaB activation in the cytoplasm and translocation into the nucleus. In contrast, the DNA binding activity of oxidized NF-kappaB is significantly diminished, and that activity is restored by reducing enzymes, such as thioredoxin or redox factor 1. This review describes the signal transduction pathways for NF-kappaB activation and redox regulation of NF-kB activation in the cytoplasm and nucleus.

摘要

还原/氧化(redox)调节介导多种细胞反应,并与多种生理疾病相关。转录因子核因子κB(NF-κB)是一种对氧化还原敏感的因子。NF-κB通过调节大量细胞因子和其他免疫反应基因的基因表达,在免疫反应和炎症中发挥核心作用。在受刺激的细胞中,NF-κB被困在细胞质中,并在包括氧化应激在内的多种刺激下转位进入细胞核。活性氧增强了NF-κB在细胞质中的激活信号转导途径以及向细胞核的转位。相反,氧化型NF-κB的DNA结合活性显著降低,而这种活性可通过还原酶(如硫氧还蛋白或氧化还原因子1)恢复。本综述描述了NF-κB激活的信号转导途径以及细胞质和细胞核中NF-κB激活的氧化还原调节。

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