Lee Sun J, Qin Hongwei, Benveniste Etty N
Department of Cell Biology, University of Alabama at Birmingham, Birmingham, AL 35294-0005, USA.
Eur J Immunol. 2008 Aug;38(8):2325-36. doi: 10.1002/eji.200838189.
Statins are 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors that exert anti-inflammatory effects. IFN-gamma induction of class II MHC expression, which requires the class II transactivator (CIITA), is inhibited by statins; however, the molecular basis for suppression is undetermined. We describe that statins inhibit IFN-gamma-induced class II MHC expression by suppressing CIITA gene expression, which is dependent on the HMG-CoA reductase pathway. In addition, CIITA expression is inhibited by GGTI-298 or Clostridium difficile Toxin A, specific inhibitors of Rho family protein prenylation, indicating the involvement of small GTPases. Rac1 is involved in IFN-gamma inducible expression of CIITA, and statins inhibit IFN-gamma-induced Rac1 activation, contributing to the inhibitory effect of statins. IFN-gamma induction of the CIITA gene is regulated by the transcription factors STAT-1alpha, interferon regulatory factor (IRF)-1 and upstream stimulatory factor (USF)-1. We previously reported that statins inhibit constitutive STAT-1alpha expression. IRF-1, a STAT-1 dependent gene, is also inhibited by statins. Therefore, statin treatment results in decreased recruitment of STAT-1alpha and IRF-1 to the endogenous CIITA promoter IV (pIV). The recruitment of USF-1 to CIITA pIV is also reduced by statins, as is the recruitment of RNA polymerase II (Pol II), p300 and Brg-1. These data indicate that statins inhibit the transcriptional program of the CIITA gene.
他汀类药物是一类具有抗炎作用的3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂。他汀类药物可抑制干扰素-γ(IFN-γ)诱导的II类主要组织相容性复合体(MHC)表达,而这一过程需要II类反式激活因子(CIITA);然而,抑制作用的分子基础尚未明确。我们发现,他汀类药物通过抑制CIITA基因表达来抑制IFN-γ诱导的II类MHC表达,且该抑制作用依赖于HMG-CoA还原酶途径。此外,Rho家族蛋白异戊二烯化的特异性抑制剂GGTI-298或艰难梭菌毒素A可抑制CIITA表达,这表明小GTP酶参与其中。Rac1参与CIITA的IFN-γ诱导性表达,他汀类药物可抑制IFN-γ诱导的Rac1激活,这有助于其发挥抑制作用。CIITA基因的IFN-γ诱导受转录因子信号转导和转录激活因子1α(STAT-1α)、干扰素调节因子(IRF)-1和上游刺激因子(USF)-1调控。我们之前报道过他汀类药物可抑制组成型STAT-1α表达。IRF-1是一种依赖于STAT-1的基因,也受到他汀类药物的抑制。因此,他汀类药物治疗会导致STAT-1α和IRF-1与内源性CIITA启动子IV(pIV)的结合减少。他汀类药物还会降低USF-1与CIITA pIV的结合,以及RNA聚合酶II(Pol II)、p300和Brg-1的结合。这些数据表明他汀类药物可抑制CIITA基因的转录程序。