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丝裂原活化蛋白激酶抑制剂通过抑制HepG2细胞中的Imp 7或Imp 8来减少磷酸化Smads的核内积累。

Mitogen-activated protein kinase inhibitors reduce the nuclear accumulation of phosphorylated Smads by inhibiting Imp 7 or Imp 8 in HepG2 cells.

作者信息

Hu Xiangpeng, Kan Hongwei, Boye Alex, Jiang Yufeng, Wu Chao, Yang Yan

机构信息

Department of Pharmacology, Institute of Natural Medicine, Anhui Medical University, Hefei, Anhui 230032, P.R. China.

Digestive Department, The Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230601, P.R. China.

出版信息

Oncol Lett. 2018 Apr;15(4):4867-4872. doi: 10.3892/ol.2018.7926. Epub 2018 Feb 2.

Abstract

The transforming growth factor (TGF)-β/Smad signaling pathway is involved in hepatocellular carcinoma development. Smad2 and Smad3 are phosphorylated following TGF-β1 stimulation and subsequently oligomerize with Smad4 to form the Smad2/3/4 complex, which translocates into the nucleus and regulates target genes, including plasminogen activator inhibitor type 1 (PAI1). Importin (Imp)7 and Imp8 are responsible for transporting phosphorylated (p)Smad2/3 and Smad4 into the nucleus. In our previous study, it was demonstrated that mitogen-activated protein kinase (MAPK) inhibitors, including inhibitors of extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK) and p38 could inhibit the transcription of PAI1, but ERK inhibitor had no significant effect on the phosphorylation of Smad2/3, and the formation of Smad2/3/4 complexes, which was different from the effect of JNK or p38 inhibitor. We hypothesized that MAPK inhibitors, particularly ERK inhibitor, reduced the transport of Smads into the nucleus by affecting Imp7 and Imp8. To confirm this hypothesis, HepG2 cells were incubated with different MAPK inhibitors for 5 h and subsequently stimulated with TGF-β1 for 1 h. Next, the intracellular locations of Smads (pSmad2C, pSmad2L, pSmad3C, pSmad3L and Smad4) and Imp7/8 were detected using immunofluorescence staining assays, and the expression of Imp7/8 was investigated using immunoblotting. It was revealed that JNK or p38 inhibitor decreased the phosphorylation of Smad2C, Smad2L and Smad3L, and affected their nuclear accumulation. Although only inhibiting the phosphorylation of Smad2C, ERK inhibitor affected the nuclear accumulation of pSmad2C, pSmad2L, pSmad3C and pSmad3L. The three MAPK inhibitors attenuated the nuclear distribution of Smad4, and the expression and nuclear accumulation of Imp7. ERK and JNK inhibitors attenuated the expression and nuclear accumulation of Imp8. Thus, the results of the present study suggest that MAPK inhibitors, particularly ERK inhibitor, modulate the nuclear accumulation of Smads via the inhibition of Imp 7/8.

摘要

转化生长因子(TGF)-β/Smad信号通路参与肝细胞癌的发展。在TGF-β1刺激后,Smad2和Smad3发生磷酸化,随后与Smad4寡聚形成Smad2/3/4复合物,该复合物转位到细胞核并调节靶基因,包括1型纤溶酶原激活物抑制剂(PAI1)。输入蛋白(Imp)7和Imp8负责将磷酸化的(p)Smad2/3和Smad4转运到细胞核中。在我们之前的研究中,已证明丝裂原活化蛋白激酶(MAPK)抑制剂,包括细胞外信号调节激酶(ERK)抑制剂、c-Jun氨基末端激酶(JNK)抑制剂和p38抑制剂,可抑制PAI1的转录,但ERK抑制剂对Smad2/3的磷酸化以及Smad2/3/4复合物的形成没有显著影响,这与JNK或p38抑制剂的作用不同。我们推测MAPK抑制剂,特别是ERK抑制剂,通过影响Imp7和Imp8减少Smads向细胞核的转运。为了证实这一假设,将HepG2细胞与不同的MAPK抑制剂孵育5小时,随后用TGF-β1刺激1小时。接下来,使用免疫荧光染色法检测Smads(pSmad2C、pSmad2L、pSmad3C、pSmad3L和Smad4)和Imp7/8的细胞内定位,并使用免疫印迹法研究Imp7/8的表达。结果显示,JNK或p38抑制剂降低了Smad2C、Smad2L和Smad3L的磷酸化,并影响它们的核积累。虽然ERK抑制剂仅抑制Smad2C的磷酸化,但它影响pSmad2C、pSmad2L、pSmad3C和pSmad3L的核积累。三种MAPK抑制剂均减弱了Smad4的核分布以及Imp7的表达和核积累。ERK和JNK抑制剂减弱了Imp8的表达和核积累。因此,本研究结果表明MAPK抑制剂,特别是ERK抑制剂,通过抑制Imp 7/8来调节Smads的核积累。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8597/5840705/21117af0743d/ol-15-04-4867-g00.jpg

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