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

机译:Phorbol 12-肉豆蔻酸酯13-醋酸盐诱导的鸡肠细胞变化

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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:增加的肠上皮渗透性与许多肠溶疾病有关,因为它允许易于访问微生物病原体和毒素进入系统。在家禽生产中,使用抗生素生长促进剂的限制增加了鸟类易受不同肠疾病的疾病的机会。因此,了解损害肠功能的机制是相关的。基于我们之前的观察结果,该观察显示培养的培养物中的培养物肠细胞进行营养不良的醋酸(PMA)进行营养不良的变化,我们抑制了这种模型,似乎模仿肠道透露性,可能有助于了解这个问题的机制。随着基因组和蛋白质组学的变化与许多生理和病理问题有关,我们感兴趣地发现某些蛋白质组学变化是否利于PMA诱导的肠细胞的形态改变。将原发性肠细胞培养物暴露于PMA的亚致死浓度,提取蛋白质,并通过质谱法分析差异调节的蛋白质。我们的研究结果表明,PMA影响了几种对其能量代谢,核活动,核心活动的生物过程,差异调节了几种应激蛋白质,伴侣,细胞骨骼和信号转导蛋白在肠细胞营养不良的原因中的水平。 Phorbol Myristate受醋酸盐影响的信号转导活动还提高了它们对病原体易感性增加的可能性。肠细胞完整性的变化可以使肠道易受微生物病原体的侵袭和破坏肠道稳态。

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