Kim Hong Sook, Ye Sang-Kyu, Cho Ik Hyun, Jung Joo Eun, Kim Dong-Hyun, Choi Seongwon, Kim Yong-Sik, Park Chung-Gyu, Kim Tae-Yoon, Lee Jung Weon, Chung Myung-Hee
Department of Pharmacology, Seoul National University College of Medicine, Chungno-gu, Seoul 110-799, Korea.
Free Radic Biol Med. 2006 Nov 1;41(9):1392-403. doi: 10.1016/j.freeradbiomed.2006.07.018. Epub 2006 Jul 27.
Free 8-hydroxydeoxyguanosine (oh(8)dG), a nucleoside of 8-hydroxyguanine (oh(8)Gua), present in cytosol is not incorporated into DNA. However, nothing is known about its biological function when it presents in cytosol as a free form. We demonstrate here for the first time that oh(8)dG inhibits lipopolysaccharide (LPS)-induced nitric oxide (NO) production and cyclooxygenase-2 (COX-2) activity, and both gene transcriptions in microglia. Furthermore, oh(8)dG reduced mRNA levels of pro-inflammatory cytokine, such as IL-1beta, IL-6, and TNF-alpha, in activated BV2 cells. We also found that oh(8)dG suppressed reactive oxygen species (ROS) production through reduction of NADPH oxidase activity and blocked Rac1/STATs signal cascade. Finally, oh(8)dG suppressed recruitment of STATs and p300 to the iNOS and COX-2 promoters, and inhibited H3 histone acetylation. Taken together, these results provide new aspects of oh(8)dG as an anti-inflammatory agent.
游离的8-羟基脱氧鸟苷(oh(8)dG)是8-羟基鸟嘌呤(oh(8)Gua)的一种核苷,存在于胞质溶胶中,不会掺入DNA。然而,当它以游离形式存在于胞质溶胶中时,其生物学功能尚不清楚。我们在此首次证明,oh(8)dG可抑制脂多糖(LPS)诱导的小胶质细胞中一氧化氮(NO)的产生和环氧合酶-2(COX-2)的活性以及这两个基因的转录。此外,oh(8)dG降低了活化的BV2细胞中促炎细胞因子如IL-1β、IL-6和TNF-α的mRNA水平。我们还发现,oh(8)dG通过降低NADPH氧化酶活性抑制活性氧(ROS)的产生,并阻断Rac1/信号转导和转录激活因子(STATs)信号级联反应。最后,oh(8)dG抑制STATs和p300募集到诱导型一氧化氮合酶(iNOS)和COX-2启动子,并抑制H3组蛋白乙酰化。综上所述,这些结果为oh(8)dG作为一种抗炎剂提供了新的视角。