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首页> 外文期刊>The Journal of Infectious Diseases >Cryptosporidium infection of human intestinal epithelial cells increases expression of osteoprotegerin: a novel mechanism for evasion of host defenses.
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Cryptosporidium infection of human intestinal epithelial cells increases expression of osteoprotegerin: a novel mechanism for evasion of host defenses.

机译:人肠上皮细胞的隐孢子虫感染增加了骨保护素的表达:一种逃避宿主防御的新机制。

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摘要

Cryptosporidium parasites are pathogens of human intestinal epithelial cells. To determine which genes are regulated during early infection, human ileal mucosa cultured as explants was infected with C. parvum or C. hominis, and gene expression was analyzed by microarray. The gene for osteoprotegerin (OPG) was up-regulated by both parasites. OPG mRNA was also significantly increased in biopsy specimens obtained from a volunteer experimentally infected with C. meleagridis, compared with levels in a prechallenge biopsy specimen. After in vitro infection of HCT-8 cells, there was an early peak in production of OPG mRNA protein. Treatment of infected cells with the OPG ligand tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induced epithelial cell apoptosis and reduced parasite numbers, and recombinant OPG blocked these effects. These results suggest a novel TRAIL-mediated pathway for elimination of Cryptosporidium infection and a role for OPG in modulating this host response.
机译:隐孢子虫寄生虫是人肠上皮细胞的病原体。为了确定在早期感染期间哪些基因受到调控,将培养为外植体的人回肠粘膜感染小球藻或人曲霉,并通过微阵列分析基因表达。两种寄生虫均上调了骨保护蛋白(OPG)的基因。与挑战前活检标本中的水平相比,从实验上感染了米氏梭菌的志愿者获得的活检标本中,OPG mRNA也显着增加。在体外感染HCT-8细胞后,OPG mRNA蛋白的产生出现了早期高峰。用OPG配体肿瘤坏死因子相关的凋亡诱导配体(TRAIL)处理感染的细胞可诱导上皮细胞凋亡并减少寄生虫数量,重组OPG阻止了这些作用。这些结果表明,新型的TRAIL介导的途径可以消除隐孢子虫感染,并且OPG在调节宿主反应中具有重要作用。

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