Park Jin Mo, Greten Florian R, Wong Athena, Westrick Randal J, Arthur J Simon C, Otsu Kinya, Hoffmann Alexander, Montminy Marc, Karin Michael
Laboratory of Gene Regulation and Signal Transduction, Department of Pharmacology, University of California-San Diego, La Jolla, CA 92093, USA.
Immunity. 2005 Sep;23(3):319-29. doi: 10.1016/j.immuni.2005.08.010.
Certain microbes evade host innate immunity by killing activated macrophages with the help of virulence factors that target prosurvival pathways. For instance, infection of macrophages with the TLR4-activating bacterium Bacillus anthracis triggers an apoptotic response due to inhibition of p38 MAP kinase activation by the bacterial-produced lethal toxin. Other pathogens induce macrophage apoptosis by preventing activation of NF-kappaB, which depends on IkappaB kinase beta (IKKbeta). To better understand how p38 and NF-kappaB maintain macrophage survival, we searched for target genes whose products prevent TLR4-induced apoptosis and a p38-dependent transcription factor required for their induction. Here we describe key roles for transcription factor CREB, a target for p38 signaling, and the plasminogen activator 2 (PAI-2) gene, a target for CREB, in maintenance of macrophage survival.
某些微生物借助靶向生存途径的毒力因子杀死活化的巨噬细胞,从而逃避宿主的固有免疫。例如,用激活TLR4的炭疽芽孢杆菌感染巨噬细胞,会因细菌产生的致死毒素抑制p38丝裂原活化蛋白激酶的激活而引发凋亡反应。其他病原体通过阻止依赖IκB激酶β(IKKβ)的核因子κB的激活来诱导巨噬细胞凋亡。为了更好地理解p38和核因子κB如何维持巨噬细胞的存活,我们寻找了其产物可预防TLR4诱导的凋亡的靶基因,以及诱导这些基因所需的p38依赖性转录因子。在此,我们描述了转录因子CREB(p38信号的靶点)和纤溶酶原激活物2(PAI-2)基因(CREB的靶点)在维持巨噬细胞存活中的关键作用。