From the Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104.
Centre for Molecular Biosciences, University of Ulster, BT52 1SA Coleraine, United Kingdom.
J Biol Chem. 2010 Oct 22;285(43):33485-33498. doi: 10.1074/jbc.M110.129353. Epub 2010 Aug 14.
Utilizing the Citrobacter rodentium-induced transmissible murine colonic hyperplasia (TMCH) model, we measured hyperplasia and NF-κB activation during progression (days 6 and 12 post-infection) and regression (days 20-34 post-infection) phases of TMCH. NF-κB activity increased at progression in conjunction with bacterial attachment and translocation to the colonic crypts and decreased 40% by day 20. NF-κB activity at days 27 and 34, however, remained 2-3-fold higher than uninfected control. Expression of the downstream target gene CXCL-1/KC in the crypts correlated with NF-κB activation kinetics. Phosphorylation of cellular IκBα kinase (IKK)α/β (Ser(176/180)) was elevated during progression and regression of TMCH. Phosphorylation (Ser(32/36)) and degradation of IκBα, however, contributed to NF-κB activation only from days 6 to 20 but not at later time points. Phosphorylation of MEK1/2 (Ser(217/221)), ERK1/2 (Thr(202)/Tyr(204)), and p38 (Thr(180)/Tyr(182)) paralleled IKKα/β kinetics at days 6 and 12 without declining with regressing hyperplasia. siRNAs to MEK, ERK, and p38 significantly blocked NF-κB activity in vitro, whereas MEK1/2-inhibitor (PD98059) also blocked increases in MEK1/2, ERK1/2, and IKKα/β thereby inhibiting NF-κB activity in vivo. Cellular and nuclear levels of Ser(536)-phosphorylated (p65(536)) and Lys(310)-acetylated p65 subunit accompanied functional NF-κB activation during TMCH. RSK-1 phosphorylation at Thr(359)/Ser(363) in cellular/nuclear extracts and co-immunoprecipitation with cellular p65-NF-κB overlapped with p65(536) kinetics. Dietary pectin (6%) blocked NF-κB activity by blocking increases in p65 abundance and nuclear translocation thereby down-regulating CXCL-1/KC expression in the crypts. Thus, NF-κB activation persisted despite the lack of bacterial attachment to colonic mucosa beyond peak hyperplasia. The MEK/ERK/p38 pathway therefore seems to modulate sustained activation of NF-κB in colonic crypts in response to C. rodentium infection.
利用柠檬酸杆菌诱导的可传播的鼠结肠增生(TMCH)模型,我们在 TMCH 的进展(感染后第 6 和 12 天)和消退(感染后第 20-34 天)阶段测量了增生和 NF-κB 的激活。NF-κB 的活性在进展时增加,伴随着细菌附着和向结肠隐窝的易位,并在第 20 天减少了 40%。然而,在第 27 和 34 天,NF-κB 的活性仍比未感染的对照高 2-3 倍。隐窝中下游靶基因 CXCL-1/KC 的表达与 NF-κB 激活动力学相关。细胞 IKKα/β(Ser(176/180))的磷酸化在 TMCH 的进展和消退过程中升高。然而,只有在第 6 至 20 天,而不是在后期,IκBα 的磷酸化(Ser(32/36))和降解才有助于 NF-κB 的激活。MEK1/2(Ser(217/221))、ERK1/2(Thr(202)/Tyr(204))和 p38(Thr(180)/Tyr(182))的磷酸化与 IKKα/β 的动力学相平行,在第 6 和 12 天没有随增生的消退而下降。MEK、ERK 和 p38 的 siRNA 在体外显著阻断了 NF-κB 的活性,而 MEK1/2 抑制剂(PD98059)也阻断了 MEK1/2、ERK1/2 和 IKKα/β 的增加,从而在体内抑制了 NF-κB 的活性。细胞和核中 Ser(536)-磷酸化(p65(536))和 Lys(310)-乙酰化 p65 亚基的水平伴随着 TMCH 期间功能性 NF-κB 的激活。细胞/核提取物中 RSK-1 的 Thr(359)/Ser(363)磷酸化和细胞 p65-NF-κB 的共免疫沉淀与 p65(536)动力学重叠。膳食果胶(6%)通过阻断 p65 丰度和核易位的增加来阻断 NF-κB 的活性,从而下调隐窝中的 CXCL-1/KC 表达。因此,尽管在增生高峰期过后,细菌不再附着在结肠黏膜上,NF-κB 的激活仍然持续。因此,MEK/ERK/p38 途径似乎调节了柠檬酸杆菌感染后结肠隐窝中 NF-κB 的持续激活。