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肿瘤坏死因子(TNFα)在沙门氏菌病期间调节肠道黏液分泌。

Tumor necrosis factor (TNF alpha) regulates intestinal mucus production during salmonellosis.

作者信息

Arnold J W, Klimpel G R, Niesel D W

机构信息

Department of Microbiology, University of Texas Medical Branch, Galveston 77555-1019.

出版信息

Cell Immunol. 1993 Oct 15;151(2):336-44. doi: 10.1006/cimm.1993.1243.

Abstract

Mucus production by goblet cells in the gastrointestinal tract following Salmonella typhimurium infection using a ligated ileal loop model in mice was investigated. Assessment of the morphology of the loop tissue after Salmonella challenge revealed generalized tissue inflammation, characterized by edema and an inflammatory cell infiltrate. Villi were shortened and blunted, and crypts contained an increased number of cells with mitotic figures. Production of TNF alpha in the loops followed Salmonella challenge and occurred at the same time as the pathological sequelae. A nearly 50% decrease in the number of goblet cells in infected tissue compared to tissue from noninfected controls was observed at these same times. The sulfation of mucins produced by the goblet cells in infected tissues was increased in the villi but was unchanged in the crypts compared to uninfected tissues. Treatment of mice with antibody to TNF alpha before Salmonella challenge abrogated tissue pathology and returned goblet cell numbers and mucin profiles to those observed in noninfected controls. Our results indicate that TNF alpha may mediate changes in goblet cell expression and mucin sulfation in response to Salmonella challenge.

摘要

利用小鼠结扎回肠袢模型,研究了鼠伤寒沙门氏菌感染后胃肠道杯状细胞的黏液分泌情况。沙门氏菌攻击后对肠袢组织形态的评估显示出广泛性组织炎症,其特征为水肿和炎性细胞浸润。绒毛缩短且变钝,隐窝中含有更多带有有丝分裂象的细胞。沙门氏菌攻击后肠袢中肿瘤坏死因子α(TNFα)产生,且与病理后遗症同时出现。在这些相同时间观察到,与未感染对照组织相比,感染组织中杯状细胞数量减少了近50%。与未感染组织相比,感染组织中杯状细胞产生的黏蛋白在绒毛中的硫酸化增加,但在隐窝中无变化。在沙门氏菌攻击前用抗TNFα抗体治疗小鼠可消除组织病理学变化,并使杯状细胞数量和黏蛋白谱恢复到未感染对照中的水平。我们的结果表明,TNFα可能介导了杯状细胞表达和黏蛋白硫酸化对沙门氏菌攻击的反应变化。

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