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在增生的进展和消退阶段,NF-κB 活性的新变化:MEK、ERK 和 p38 的作用。

Novel changes in NF-{kappa}B activity during progression and regression phases of hyperplasia: role of MEK, ERK, and p38.

机构信息

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.

出版信息

J Biol Chem. 2010 Oct 22;285(43):33485-33498. doi: 10.1074/jbc.M110.129353. Epub 2010 Aug 14.

Abstract

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.

摘要

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。

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