Uesugi Shota, Muroi Makoto, Kondoh Yasumitsu, Shiono Yoshihito, Osada Hiroyuki, Kimura Ken-Ichi
The United Graduate School of Agricultural Sciences, Iwate University, Iwate, Japan.
RIKEN Center for Sustainable Resource Science (CSRS), Saitama, Japan.
J Antibiot (Tokyo). 2017 Apr;70(4):429-434. doi: 10.1038/ja.2016.99. Epub 2016 Aug 10.
Keap1-Nrf2 system is known as a sensor of electrophilic compounds, and protects cells from oxidative stress through induction of various antioxidant enzymes. We found by proteomic analysis that allantopyrone A, a metabolite isolated from an endophytic fungus, upregulates the expression of proteins that are regulated by the transcription factor Nrf2. Indeed, allantopyrone A increased the antioxidant enzyme heme oxygenase-1 in PC12 cells. Moreover, it induced localization of Nrf2 in the nucleus. Affinity purification of allantopyrone A-binding protein showed that this compound could bind directly to Keap1. Allantopyrone A suppressed intracellular reactive oxygen species level and cell death induced by HO in PC12 cells. These results indicate that allantopyrone A protects PC12 cells from oxidative stress-induced cell death through direct binding with Keap1 and activation of the Keap1-Nrf2 pathway.
Keap1-Nrf2系统被认为是亲电化合物的传感器,并通过诱导各种抗氧化酶来保护细胞免受氧化应激。我们通过蛋白质组学分析发现,从一种内生真菌中分离出的代谢产物尿囊吡喃酮A上调了受转录因子Nrf2调控的蛋白质的表达。事实上,尿囊吡喃酮A增加了PC12细胞中抗氧化酶血红素加氧酶-1的含量。此外,它还诱导了Nrf2在细胞核中的定位。尿囊吡喃酮A结合蛋白的亲和纯化表明,该化合物可直接与Keap1结合。尿囊吡喃酮A抑制了PC12细胞中细胞内活性氧水平和HO诱导的细胞死亡。这些结果表明,尿囊吡喃酮A通过与Keap1直接结合并激活Keap1-Nrf2途径,保护PC12细胞免受氧化应激诱导的细胞死亡。