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8-羟基脱氧鸟苷通过Rac1/信号转导和转录激活因子信号通路抑制脂多糖诱导的脑小胶质细胞中一氧化氮的产生和环氧化酶-2的活性。

8-hydroxydeoxyguanosine suppresses NO production and COX-2 activity via Rac1/STATs signaling in LPS-induced brain microglia.

作者信息

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

机构信息

Department of Pharmacology, Seoul National University College of Medicine, Chungno-gu, Seoul 110-799, Korea.

出版信息

Free Radic Biol Med. 2006 Nov 1;41(9):1392-403. doi: 10.1016/j.freeradbiomed.2006.07.018. Epub 2006 Jul 27.

Abstract

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.

摘要

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。

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