南方医科大学学报 ›› 2016, Vol. 36 ›› Issue (06): 819-.

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Muc2基因沉默可降低益生菌抑制大肠杆菌黏附和侵袭的能力

邱嘉文,何肖龙,张宝,杜蕾,曾庆,李森,熊欢欢,龙敏,罗军,曹虹   

  • 出版日期:2016-06-20 发布日期:2016-06-20

Effect on Muc2 gene knockdown in Ht29 cells by CRISPR/Cas9 on probiotics-mediated inhibition of E.coli K1 adhesion and invasion

  • Online:2016-06-20 Published:2016-06-20

摘要: 目的建立抑制肠上皮细胞基因组中Muc2 基因表达的CRISPR/Cas9 系统并探索粘蛋白Muc2 在鼠李糖乳杆菌GG株 (LGG)抑制大肠杆菌K1(Escherichia coli, E.coli k1)株E44 黏附和侵袭肠上皮中的作用机制。方法设计2 个长20~25 bp 的 sgRNA分别靶向Muc2,合成sgRNA寡核苷酸序列并构建CRISPR表达载体,转染野生型人结肠癌Ht29细胞,蛋白免疫印迹法 检测抑制效率及通过MTT法检测其细胞活力及生长情况后,竞争性排斥分析验证粘蛋白Muc2在益生菌抑制E44黏附侵袭肠 上皮中的作用。结果目的sgRNA寡核苷酸双链成功插入酶切后的lenticrisprv2质粒载体中且序列正确;稳定抑制Muc2表达的 细胞株筛选成功;Muc2基因沉默后,与空白对照组相比,其表达水平明显降低,抑制率可达81%(P<0.01);黏附侵袭实验中E44 相对黏附率为72.23%(P<0.01),相对侵袭率为81.49%(P<0.01),益生菌LGG的抑制E44 黏附和侵袭作用明显下调。结论 Muc2基因下调明显降低益生菌抑制E44黏附和侵袭肠上皮细胞的能力,提示益生菌刺激Muc2表达上调可能是其强化加固肠粘 膜屏障和拮抗致病菌功能的关键性机制之一,并可为肠道细菌性感染疾病的预防治疗提供了一个新手段。

Abstract: Objective To investigate the effects of Lactobacillus rhamnosus GG (LGG) for inhibiting E.coli K1 (E44) adhesion and invasion of an intestinal epithelial cell model with Muc2 gene knockdown established using CRISPR-Cas9 system. Methods Two 20-25 bp sgRNAs targeting Muc2 were chemically synthesized to construct CRISPR expression vectors for transfection in wild-type human colonic cancer cell line Ht29. The efficiency of Muc2 knockdown was determined using Western blotting. After assessment of the viability and proliferation of the transfected cells with MTT assay, we evaluated the effects of the probiotics against E44 adhesion and invasion of the cells through a competitive exclusion assay. Results Transfection of the cells with Lenticrisprv2 plasmid vectors resulted in a cell line with stable Muc2 knockdown by 81%. The inhibitory effects of probiotics against E44 adhesion and invasion of the transfected cells were markedly attenuated, and the relative adhesion and invasion rates of E44 were 72.23% (P<0.05) and 81.49% (P<0.05), respectively. Conclusion Muc2 knockdown causes attenuation of the inhibitory effects of probiotics against E44 adhesion and invasion of the intestinal epithelial cells, suggesting that up-regulation of Muc2 may serve as an important mechanism for the probiotics to reinforce the intestinal barrier and antagonize the pathogenic bacteria, which sheds light on a new strategy for prevention and treatment of bacterial intestinal infections.