首页> 美国卫生研究院文献>International Journal of Molecular Sciences >gga-miR-451 Negatively Regulates Mycoplasma gallisepticum (HS Strain)-Induced Inflammatory Cytokine Production via Targeting YWHAZ
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gga-miR-451 Negatively Regulates Mycoplasma gallisepticum (HS Strain)-Induced Inflammatory Cytokine Production via Targeting YWHAZ

机译:gga-miR-451通过靶向YWHAZ负调控鸡支原体(HS株)诱导的炎性细胞因子生产

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摘要

Mycoplasma gallisepticum (MG) is the most economically significant mycoplasma pathogen of poultry that causes chronic respiratory disease (CRD) in chickens. Although miRNAs have been identified as a major regulator effect on inflammatory response, it is largely unclear how they regulate MG-induced inflammation. The aim of this study was to investigate the functional roles of gga-miR-451 and identify downstream targets regulated by gga-miR-451 in MG infection of chicken. We found that the expression of gga-miR-451 was significantly up-regulated during MG infection of chicken embryo fibroblast cells (DF-1) and chicken embryonic lungs. Overexpression of gga-miR-451 decreased the MG-induced inflammatory cytokine production, including tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6), whereas inhibition of gga-miR-451 had the opposite effect. Gene expression data combined with luciferase reporter assays demonstrated that tyrosine3-monooxygenase/tryptophan5-monooxygenase activation protein zeta (YWHAZ) was identified as a direct target of gga-miR-451 in the context of MG infection. Furthermore, upregulation of gga-miR-451 significantly inhibited the MG-infected DF-1 cells proliferation, induced cell-cycle arrest, and promoted apoptosis. Collectively, our results demonstrate that gga-miR-451 negatively regulates the MG-induced production of inflammatory cytokines via targeting YWHAZ, inhibits the cell cycle progression and cell proliferation, and promotes cell apoptosis. This study provides a better understanding of the molecular mechanisms of MG infection.
机译:鸡支原体支原体(MG)是家禽中最具经济意义的支原体病原体,可引起鸡的慢性呼吸道疾病(CRD)。尽管已确定miRNA是炎症反应的主要调节剂,但目前尚不清楚它们如何调节MG诱导的炎症。这项研究的目的是调查gga-miR-451的功能作用,并确定由gga-miR-451调控的下游靶点在鸡的MG感染中的作用。我们发现,在鸡胚成纤维细胞(DF-1)和鸡胚肺部MG感染过程中,gga-miR-451的表达明显上调。 gga-miR-451的过表达降低了MG诱导的炎性细胞因子的产生,包括肿瘤坏死因子-α(TNF-α),白介素-1β(IL-1β)和白介素-6(IL-6),而抑制gga-miR-451具有相反的效果。基因表达数据与萤光素酶报告基因分析相结合表明,在MG感染的情况下,酪氨酸3单加氧酶/色氨酸5单加氧酶激活蛋白zeta(YWHAZ)被确定为gga-miR-451的直接靶标。此外,gga-miR-451的上调显着抑制了MG感染的DF-1细胞增殖,诱导了细胞周期停滞并促进了细胞凋亡。总的来说,我们的结果表明gga-miR-451通过靶向YWHAZ负调节MG诱导的炎性细胞因子的产生,抑制细胞周期进程和细胞增殖,并促进细胞凋亡。这项研究为MG感染的分子机制提供了更好的理解。

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