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JAK2-ERK1/2-STAT3信号通路对PHLDA1表达的调控

Regulation of PHLDA1 Expression by JAK2-ERK1/2-STAT3 Signaling Pathway.

作者信息

Lyu Ji Hyo, Huang Bin, Park Dae-Weon, Baek Suk-Hwan

机构信息

Department of Biochemistry and Molecular Biology, College of Medicine, Yeungnam University, 170 Hyeonchung-ro, Nam-gu, Daegu, 705-703, South Korea.

出版信息

J Cell Biochem. 2016 Feb;117(2):483-90. doi: 10.1002/jcb.25296.

Abstract

Toll-like receptor 2 (TLR2)-mediated signaling cascades and gene regulation are mainly involved in diseases, such as immunity and inflammation. In this study, microarray analysis was performed using bone marrow-derived macrophages (BMDM) and Raw 264.7 cells to identify novel proteins involved in the TLR2-mediated cellular response. We found that pleckstrin homology-like domain family, member 1 (PHLDA1) is a novel gene up-regulated by TLR2 stimulation and determined the unique signaling pathway for its expression. Treatment with TLR2 agonist Pam3 CSK4 increased mRNA, protein, and fluorescence staining of PHLDA1. Induction of PHLDA1 by TLR2 stimulation disappeared from TLR2 KO mice-derived BMDM. Among janus kinase (JAK) family members, JAK2 was involved in TLR2-stimulated PHLDA1 expression. Signal transducer and activator of transcription 3 (STAT3) also participated in PHLDA1 expression downstream of the JAK2. Interestingly, ERK1/2 was an intermediate between JAK2 and STAT3. In silico analysis revealed the presence of highly conserved γ-activated sites within mouse PHLDA1 promoter and confirmed the JAK2-STAT3 pathway is important to Pam3 CSK4 -induced PHLDA1 transcription. These findings suggest that the JAK2-ERK1/2-STAT3 pathway is an important signaling pathway for PHLDA1 expression and that these proteins may play a critical role in eliciting TLR2-mediated immune and inflammatory response.

摘要

Toll样受体2(TLR2)介导的信号级联反应和基因调控主要涉及免疫和炎症等疾病。在本研究中,使用骨髓来源的巨噬细胞(BMDM)和Raw 264.7细胞进行微阵列分析,以鉴定参与TLR2介导的细胞反应的新蛋白。我们发现,普列克底物蛋白同源样结构域家族成员1(PHLDA1)是一种受TLR2刺激上调的新基因,并确定了其表达的独特信号通路。用TLR2激动剂Pam3 CSK4处理可增加PHLDA1的mRNA、蛋白质和荧光染色。TLR2刺激诱导的PHLDA1在TLR2基因敲除小鼠来源的BMDM中消失。在janus激酶(JAK)家族成员中,JAK2参与了TLR2刺激的PHLDA1表达。信号转导子和转录激活子3(STAT3)也参与了JAK2下游的PHLDA1表达。有趣的是,ERK1/2是JAK2和STAT3之间的中间体。计算机分析揭示了小鼠PHLDA1启动子内存在高度保守的γ激活位点,并证实JAK2-STAT3通路对Pam3 CSK4诱导的PHLDA1转录很重要。这些发现表明,JAK2-ERK1/2-STAT3通路是PHLDA1表达的重要信号通路,并且这些蛋白可能在引发TLR2介导的免疫和炎症反应中起关键作用。

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