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首页> 外文期刊>Journal of immunology research. >Knockdown of YAP/TAZ Inhibits the Migration and Invasion of Fibroblast Synovial Cells in Rheumatoid Arthritis by Regulating Autophagy
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Knockdown of YAP/TAZ Inhibits the Migration and Invasion of Fibroblast Synovial Cells in Rheumatoid Arthritis by Regulating Autophagy

机译:YAP / TAZ的敲低通过调节自噬来抑制成纤维细胞在类风湿性关节炎中的迁移和侵袭

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The purpose of this study was to investigate the effect of knockdown of the yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) on the migration and invasion of the rheumatoid arthritis fibroblast-like synoviocytes (RA-FLS) and to preliminarily elucidate the mechanisms between YAP/TAZ and autophagy in the migration and invasion of RA-FLS. RA-FLS stable knockdown of YAP or TAZ was successfully established by using lentiviral-mediated gene knockdown techniques. Wound healing assay and Transwell assay were used to evaluate the effect of knockdown of YAP or TAZ on the migration and invasion of RA-FLS. Reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) and western blotting assays were performed to examine the expression of indicated genes. The results showed that YAP and TAZ were upregulated in RA-FLS, and knockdown of YAP or TAZ inhibited the migration and invasion, reduced the expression of N-cadherin and Vimentin, and increased the accumulation of E-cadherin and β-catenin in RA-FLS. Our results also demonstrated that knockdown of YAP or TAZ promoted autophagy which increased the accumulation of LC3B-II and ULK1 and decreased the amount of SQSTM1/p62 in RA-FLS. Furthermore, our data displayed that inhibition of autophagy either with 3-MA or CQ can partially reverse the decrease of migration and invasion induced by YAP and TAZ knockdown in RA-FLS. Our experiments preliminarily revealed that YAP/TAZ and autophagy play important roles in the migration and invasion of RA-FLS, which might provide novel targets for the treatment of RA.
机译:本研究的目的是探讨对Yes相关蛋白质(yap)和转录共同激活子与PDZ结合基序(TAZ)对类风湿性关节炎成纤维细胞样Synociocytes(RA-FL)的迁移和侵袭的影响并初步阐明在迁移和入侵RA-FLS中的YAP / TAZ和自噬之间的机制。通过使用慢病毒介导的基因敲低技术成功建立了rA-FLS稳定的yap或TAZ的敲低。伤口愈合测定和Transwell测定用于评估YAP或TAZ敲低对RA-FLS的迁移和侵袭的影响。进行逆转录定量实时聚合酶链反应(RT-QPCR)和蛋白质印迹测定以检查表达的基因。结果表明,在RA-FLS上上调YAP和TAZ,yap或TAZ的敲低抑制了迁移和侵袭,降低了N-cadherin和Vimentin的表达,并增加了e-cadherin和β-catenin在Ra中的积累-fls。我们的结果还证明了YAP或TAZ的敲低促进了增加LC3B-II和ULK1的自噬,并降低了RA-FLS中的SQSTM1 / P62的量。此外,我们的数据显示在3 mA或CQ中抑制自噬能量可以部分地逆转由YAP和TAZ在RA-FLS中诱导的迁移和侵袭的降低。我们的实验初步揭示了YAP / TAZ和自噬在RA-FLS的迁移和入侵中发挥着重要作用,这可能为治疗RA提供新的目标。

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