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作 者:宋丽丽[1] 叶钧[1] 刘韵[1] 潘琼[1] 钟小莉[1] 李姗姗[1] 田音[1] 彭志红[1] 汪荣泉[1]
机构地区:[1]第三军医大学西南医院全军消化病研究所,重庆400038
出 处:《解放军医学杂志》2013年第10期826-829,共4页Medical Journal of Chinese People's Liberation Army
基 金:国家自然科学基金(81170340)~~
摘 要:目的探讨肠上皮细胞O型糖链的合成阻滞对该细胞肠分化标记物MUC2表达及细菌黏附的影响。方法采用O型糖链抑制剂benzyl-α-GalNAc抑制结肠上皮细胞HT-29及其分化型细胞(HT-29-Gal)O型糖链的合成,经benzyl-α-GalNAc处理的HT-29和HT-29-Gal细胞分别命名为HT-29-OBN和HT-29-Gal-OBN。采用Real-time PCR和Western blotting方法检测上述4种细胞中MUC2基因的转录和蛋白表达水平,并将上述细胞与致病性大肠埃希菌(EPEC)和肠出血性大肠埃希菌(EHEC)O157:H7共培养,采用系列稀释菌落计数法观察细菌在上述细胞表面的黏附情况。结果 Realtime PCR和Western blotting结果显示,经benzyl-α-GalNAc处理后,HT-29和HT-29-Gal细胞MUC2的mRNA和蛋白表达均明显减少(P<0.05)。HT-29-OBN和HT-29-Gal-OBN细胞与致病性大肠埃希菌EPEC和EHEC O157:H7的黏附明显少于HT-29和HT-29-Gal细胞(P<0.05)。结论抑制肠上皮细胞O型糖链的合成可阻碍细菌黏附及MUC2的表达。Objective To investigate the effect of O-glycosylation inhibition in intestinal epithelial cells on the expression of Mucin 2 (MUC2) and bacterial adherence. Methods Intestinal epithelial cells HT-29 and differentiated HT-29 cells (HT-29- Gal) were treated with an inhibitor of O-glycosylation (benzyl- α -GalNAc), and then named as HT-29-OBN and HT-29-Gal-OBN, respectively. The mRNA and protein expression of MUC2 in HT-29, HT29-Gal, HT-29-OBN and HT-29-Gal-OBN were detected by real-time PCR and Western blotting. Then the four kinds of above cells were incubated with enteropathogenic Escherichia coli (EPEC) or enterohemorrhagic Eschcrichia coli serotype O157:H7 (EHEC O157:HT). The bacteria were quantified by determining the colony forming unit (CFU) following the plating of serial dilutions of the bacteria to evaluate the effect of benzyl-α -GalNAc on bacteria adherence. Results The results of real-time PCR and Western blotting showed that the mRNA and protein expression levels of MUC2 in HT-29-OBN and HT-29-Gal-OBN cells were significantly lower than those in the untreated cells HT-29 and HT- 29-Gal (P〈0.05). The bacterial adherence assay showed that the adherence of EPEC and EHEC O157:H7 to HT-29-OBN and HT- 29-Gal-OBN cells significantly decreased compared with that to HT-29 and HT-29-Gal cells (P〈0.05). Conclusion Inhibition of O-glycosylation in intestinal epithelial cells may reduce the bacteria adherence and MUC2 expression.
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