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Upregulation of MMP-9 in MDCK epithelial cell line in response to expression of the Snail transcription factor

机译:Snail转录因子表达对MDCK上皮细胞系MMP-9的上调

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摘要

Overexpression of the transcription factor Snail in epithelial MDCK cells promotes the epithelial-mesenchymal transition (EMT) and the acquisition of an invasive phenotype. We report here that the expression of Snail is associated with an increase in the promoter activity and expression of the matrix metalloproteinase MMP-9. The effect of Snail silencing on MMP-9 expression corroborates this finding. Induced transcription of MMP-9 by Snail is driven by a mechanism dependent on the MAPK and phosphoinositide 3-kinase (PI3K) signalling pathways. Although other regions of the promoter were required for a complete stimulation by Snail, a minimal fragment (nucleotides -97 to +114) produces a response following an increased phosphorylation of Sp-1 and either Sp-1 or Ets-1 binding to the GC-box elements contained in this region. The expression of a dominant negative form of MEK decreased these complexes. A moderate increase in the binding of the nuclear factor kappa B (NF kappa B) to the upstream region (nucleotide -562) of the MMP-9 promoter was also observed in Snail-expressing cells. Interestingly, oncogenic H-Ras (RasV12) synergistically co-operates with Snail in the induction of MMP-9 transcription and expression. Altogether, these results indicate that MMP-9 transcription is activated in response to Snail expression and that it might explain, at least in part, the invasive properties of the Snail-expressing cells.
机译:转录因子Snail在上皮MDCK细胞中的过表达促进了上皮-间质转化(EMT)和侵袭性表型的获得。我们在这里报告Snail的表达与启动子活性和基质金属蛋白酶MMP-9的表达增加有关。蜗牛沉默对MMP-9表达的影响证实了这一发现。 Snail诱导的MMP-9转录受依赖于MAPK和磷酸肌醇3激酶(PI3K)信号通路的机制驱动。尽管Snail完全刺激需要启动子的其他区域,但Sp-1的磷酸化增加以及Sp-1或Ets-1与GC的结合增加后,最小片段(核苷酸-97至+114)仍会产生响应-box元素包含在此区域中。 MEK显性负型表达降低了这些复合物。在表达Snail的细胞中也观察到了核因子κB(NFκB)与MMP-9启动子上游区域(核苷酸-562)的结合程度的适度增加。有趣的是,致癌性H-Ras(RasV12)与Snail协同合作诱导MMP-9转录和表达。总而言之,这些结果表明,MMP-9转录响应Snail表达而被激活,并且至少可以部分解释Snail表达细胞的侵袭特性。

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