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首页> 外文期刊>Veterinary Immunology and Immunopathology >Proteomic alteration of porcine intestinal epithelial cells after pretreatment with Lactobacillus plantarum followed by infection with enterotoxigenic Escherichia coli F4
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Proteomic alteration of porcine intestinal epithelial cells after pretreatment with Lactobacillus plantarum followed by infection with enterotoxigenic Escherichia coli F4

机译:用乳酸杆菌预处理后猪肠上皮细胞的蛋白质组学改变,其用肠毒素大肠杆菌F4感染

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摘要

Enterotoxigenic Escherichia coli (ETEC) F4 causes diarrhea in infants and weaned piglets. The technique of isobaric tags for relative and absolute quantitation (iTRAQ) was used in this study to determine the differentially expressed proteins in porcine intestinal epithelial cells (IPEC-J2) after pretreatment with Lactobacillus plantarum (LP) followed by challenge with ETEC F4. A total of 4771 proteins were identified in IPEC-J2 cells, with 90, 105, and 134 differentially expressed proteins in cells exposed to ETEC, LP, and LP + ETEC, respectively. The COG analysis divided the identified proteins into 20 categories. The GO and KEGG annotation indicated that most of the differentially expressed proteins were enriched in various biological metabolism including cell cycle control, cell division and differentiation. Additionally, western blotting analyses confirmed the reduced abundance of selected proteins of the mTOR and MAPK signal pathways affected by ETEC F4. Moreover, LP pretreatment increased JNK activation in IPEC-J2 cells infected with ETEC F4. These results may provide further insights into the mechanisms involved in the interaction between ETEC F4 and intestinal epithelial cells, and broaden the understanding of the protective effects of LP in alleviating ETEC-provoked diarrhea of piglets.
机译:肠毒素大肠杆菌(ETEC)F4导致婴儿和断奶仔猪的腹泻。在该研究中使用了相对和绝对定量(ITRAQ)的等因素标签的技术,以在用乳酸杆菌(LP)预处理后测定猪肠上皮细胞(IPEC-J2)中的差异表达蛋白质,然后用​​ETEC F4攻击。在IPEC-J2细胞中鉴定了4771个蛋白质,分别在暴露于ETEC,LP和LP + ETEC的细胞中,90,105和134个差异表达的蛋白质。 COG分析将所识别的蛋白分为20类。 Go和Kegg注释表明,大多数差异表达的蛋白质在各种生物代谢中富集,包括细胞周期控制,细胞分裂和分化。此外,Western印迹分析证实了受ETEC F4影响的MTOR和MAPK信号途径的较低的富含蛋白质。此外,LP预处理增加了IPEC-J2细胞中的JNK激活,感染了ETEC F4。这些结果可以提供进一步的见解,进一步了解涉及ETEC F4和肠上皮细胞之间的相互作用的机制,并扩大了对LP缓解ETEC激发仔猪腹泻的保护作用的理解。

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