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驱蛔虫与肠道中血管生成素 4 的表达增加和杯状细胞内粘蛋白酸度增加有关。

Expulsion of Trichuris muris is associated with increased expression of angiogenin 4 in the gut and increased acidity of mucins within the goblet cell.

机构信息

Faculty of Life Sciences, University of Manchester, Manchester, M13 9PT, UK.

出版信息

BMC Genomics. 2009 Oct 24;10:492. doi: 10.1186/1471-2164-10-492.

Abstract

BACKGROUND

Trichuris muris in the mouse is an invaluable model for infection of man with the gastrointestinal nematode Trichuris trichiura. Three T. muris isolates have been studied, the Edinburgh (E), the Japan (J) and the Sobreda (S) isolates. The S isolate survives to chronicity within the C57BL/6 host whereas E and J are expelled prior to reaching fecundity. How the S isolate survives so successfully in its host is unclear.

RESULTS

Microarray analysis was used as a tool to identify genes whose expression could determine the differences in expulsion kinetics between the E and S T. muris isolates. Clear differences in gene expression profiles were evident as early as day 7 post-infection (p.i.). 43 probe sets associated with immune and defence responses were up-regulated in gut tissue from an E isolate-infected C57BL/6 mouse compared to tissue from an S isolate infection, including the message for the anti-microbial protein, angiogenin 4 (Ang4). This led to the identification of distinct differences in the goblet cell phenotype post-infection with the two isolates.

CONCLUSION

Differences in gene expression levels identified between the S and E-infected mice early during infection have furthered our knowledge of how the S isolate persists for longer than the E isolate in the C57BL/6 mouse. Potential new targets for manipulation in order to aid expulsion have been identified. Further we provide evidence for a potential new marker involving the acidity of the mucins within the goblet cell which may predict outcome of infection within days of parasite exposure.

摘要

背景

鼠类旋毛虫是感染人肠道寄生虫鞭虫的宝贵模型。已经研究了三种鼠类旋毛虫分离株,即爱丁堡(E)、日本(J)和索布雷达(S)分离株。S 分离株在 C57BL/6 宿主中存活至慢性期,而 E 和 J 在达到生育力之前被排出。S 分离株在其宿主中如此成功地存活的原因尚不清楚。

结果

微阵列分析被用作一种工具,以确定决定 E 和 S T. muris 分离株排出动力学差异的表达基因。早在感染后第 7 天(p.i.),就明显存在基因表达谱的差异。与 S 分离株感染的组织相比,来自 E 分离株感染的 C57BL/6 小鼠肠道组织中 43 个与免疫和防御反应相关的探针集上调,包括抗菌蛋白血管生成素 4(Ang4)的mRNA。这导致在感染两种分离株后,杯状细胞表型存在明显差异。

结论

在感染早期,S 和 E 感染小鼠之间鉴定的基因表达水平差异进一步加深了我们对 S 分离株在 C57BL/6 小鼠中比 E 分离株持续时间更长的认识。已经确定了用于促进排出的潜在新目标。此外,我们提供了涉及杯状细胞内粘蛋白酸度的潜在新标志物的证据,该标志物可能在寄生虫暴露后几天内预测感染的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bf1/2774869/80f6c290d2d1/1471-2164-10-492-1.jpg

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