Lee Sun-Hye, Lee Jin-Gu, Kim Jae-Ryong, Baek Suk-Hwan
Aging-associated Vascular Disease Research Center, Department of Biochemistry & Molecular Biology, College of Medicine, Yeungnam University, 317-1 Daemyung-5 Dong, Daegu 705-717, South Korea.
Biochem Biophys Res Commun. 2007 Dec 28;364(4):996-1001. doi: 10.1016/j.bbrc.2007.10.111. Epub 2007 Oct 26.
Although CpG containing DNA is an important regulator of innate immune responses via toll-like receptor 9 (TLR9), excessive activation of this receptor is detrimental to the host. Here, we show that cytosolic phospholipase A(2) (cPLA(2)) activation is important for TLR9-mediated inducible nitric oxide synthase (iNOS) expression. Activation of TLR9 signaling by CpG induces iNOS expression and NO production. Inhibition of TLR9 blocked the iNOS expression and NO production. The CpG also stimulates cPLA(2)-hydrolyzed arachidonic acid (AA) release. Inhibition of cPLA(2) activity by inhibitor attenuated the iNOS expression by CpG response. Additionally, knockdown of cPLA(2) protein by miRNA also suppressed the CpG-induced iNOS expression. Furthermore, the CpG rapidly phosphorylates three MAPKs and Akt. A potent inhibitor for p38 MAPK or Akt blocked the CpG-induced AA release and iNOS expression. These results suggest that TLR9 activation stimulates cPLA(2) activity via p38 or Akt pathways and mediates iNOS expression.
尽管含CpG的DNA是通过Toll样受体9(TLR9)对先天性免疫反应的重要调节因子,但该受体的过度激活对宿主有害。在此,我们表明胞质磷脂酶A2(cPLA2)的激活对于TLR9介导的诱导型一氧化氮合酶(iNOS)表达很重要。CpG激活TLR9信号传导可诱导iNOS表达和NO产生。抑制TLR9可阻断iNOS表达和NO产生。CpG还刺激cPLA2水解花生四烯酸(AA)的释放。用抑制剂抑制cPLA2活性可减弱CpG反应诱导的iNOS表达。此外,通过miRNA敲低cPLA2蛋白也可抑制CpG诱导的iNOS表达。此外,CpG可迅速使三种丝裂原活化蛋白激酶(MAPK)和Akt磷酸化。p38 MAPK或Akt的有效抑制剂可阻断CpG诱导的AA释放和iNOS表达。这些结果表明,TLR9激活通过p38或Akt途径刺激cPLA2活性并介导iNOS表达。