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Phorbol 12-Myristate 13-Acetate-Induced Changes in Chicken Enterocytes

机译:Phorbol 12-肉豆蔻酸13-乙酸盐引起的鸡肠上皮细胞变化

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摘要

Increased intestinal epithelial permeability has been linked to many enteric diseases because it allows easy access of microbial pathogens and toxins into the system. In poultry production, the restrictions in the use of antibiotic growth promoters have increased the chances of birds being susceptible to different enteric diseases. Thus, understanding the mechanisms which compromise intestinal function is pertinent. Based on our previous observation which showed the primary chicken enterocytes in culture undergoing dystrophic changes on treatment with phorbol myristate acetate (PMA), we surmised that this model, which appeared to mimic increased intestinal permeability, may help to understand the mechanisms of this problem. As genomic and proteomic changes are associated with many physiological and pathological problems, we were interested to find whether certain proteomic changes underlie the morphological alterations in the enterocytes induced by PMA. We exposed primary enterocyte cultures to a sub-lethal concentration of PMA, extracted the proteins, and analyzed by mass spectrometry for differentially regulated proteins. Our results showed that PMA affected several biological processes which negatively affected their energy metabolism, nuclear activities, and differentially regulated the levels of several stress proteins, chaperon, cytoskeletal, and signal transduction proteins that appear to be relevant in the cause of enterocyte dystrophy. Phorbol myristate acetate-affected signal transduction activities also raise the possibilities of their increased susceptibility to pathogens. The changes in enterocyte integrity can make intestine vulnerable to invasion by microbial pathogens and disrupt gut homeostasis.
机译:肠道上皮通透性增加与许多肠道疾病有关,因为它使微生物病原体和毒素易于进入系统。在家禽生产中,对抗生素生长促进剂的使用限制增加了禽类易患不同肠道疾病的机会。因此,了解损害肠道功能的机制是适当的。基于我们先前的观察结果,该结果显示了佛波肉豆蔻酸酯乙酸酯(PMA)处理后培养物中的原代鸡肠细胞发生营养不良的变化,我们推测该模型似乎模拟了肠道通透性的增加,可能有助于了解此问题的机制。由于基因组和蛋白质组学变化与许多生理和病理学问题相关,因此我们有兴趣了解某些蛋白质组学变化是否是PMA诱导的肠细胞形态改变的基础。我们将初级肠上皮细胞培养物暴露于亚致死浓度的PMA,提取蛋白质,并通过质谱分析差异调节的蛋白质。我们的结果表明,PMA影响了几个生物过程,这些过程对其能量代谢,核活动产生了负面影响,并差异性调节了几种与肠细胞营养不良的原因有关的应激蛋白,分子伴侣,细胞骨架和信号转导蛋白的水平。醋酸肉豆蔻酸乙酸酯影响的信号转导活性也增加了其对病原体敏感性的可能性。肠上皮细胞完整性的变化可使肠道容易受到微生物病原体的侵袭,并破坏肠道稳态。

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