Brobeil Alexander, Kämmerer Fabian, Tag Claudia, Steger Klaus, Gattenlöhner Stefan, Wimmer Monika
Institute of Anatomy and Cell Biology, Justus-Liebig-University, Gießen 35392, Germany.
Institute of Pathology, Justus-Liebig-University, Gießen 35392, Germany.
Biomolecules. 2015 Apr 16;5(2):485-504. doi: 10.3390/biom5020485.
The present study shows a new connection of protein tyrosine phosphatase interacting protein 51 (PTPIP51) to the nuclear factor κB (NFκB) signalling pathway. PTPIP51 mRNA and protein expression is regulated by RelA. If bound to the PTPIP51 promoter, RelA repress the mRNA and protein expression of PTPIP51. The parallel treatment with pyrrolidine dithiocarbamate (PDTC) reversed the suppression of PTPIP51 protein expression induced by TNFα. Using the intensity correlation analysis PTPIP51 verified a co-localization with RelA, which is also regulated by TNFα administration. Moreover, the direct interaction of PTPIP51 and RelA was established using the DuoLink proximity ligation assay. IκBα, the known inhibitor of RelA, also interacted with PTPIP51. This hints to the fact that in un-stimulated conditions PTPIP51 forms a complex with RelA and IκBα. The PTPIP51/RelA/IκBα complex is modulated by TNFα. Interestingly, the impact on the mitogen activated protein kinase pathway was negligible except in highest TNFα concentration. Here, PTPIP51 and Raf-1 interactions were slightly repressed. The newly established relationship of PTPIP51 and the NFκB signaling pathway provides the basis for a possible therapeutic impact.
本研究揭示了蛋白酪氨酸磷酸酶相互作用蛋白51(PTPIP51)与核因子κB(NFκB)信号通路的一种新联系。PTPIP51的mRNA和蛋白表达受RelA调控。当RelA与PTPIP51启动子结合时,会抑制PTPIP51的mRNA和蛋白表达。用吡咯烷二硫代氨基甲酸盐(PDTC)进行平行处理可逆转TNFα诱导的PTPIP51蛋白表达抑制。通过强度相关分析,PTPIP51证实与RelA共定位,RelA也受TNFα给药的调控。此外,使用DuoLink邻近连接分析确定了PTPIP51与RelA的直接相互作用。RelA的已知抑制剂IκBα也与PTPIP51相互作用。这暗示在未受刺激的条件下,PTPIP51与RelA和IκBα形成复合物。PTPIP51/RelA/IκBα复合物受TNFα调节。有趣的是,除了在最高TNFα浓度下,对丝裂原活化蛋白激酶途径的影响可忽略不计。在此情况下,PTPIP51与Raf-1的相互作用略有抑制。新建立的PTPIP51与NFκB信号通路的关系为可能的治疗作用提供了基础。