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首页> 外文期刊>American Journal of Pathology >Aberrant Mucosal Mast Cell Protease Expression in the Enteric Epithelium of Nematode-Infected Mice Lacking the Integrin αvß6, a Transforming Growth Factor-ß1 Activator
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Aberrant Mucosal Mast Cell Protease Expression in the Enteric Epithelium of Nematode-Infected Mice Lacking the Integrin αvß6, a Transforming Growth Factor-ß1 Activator

机译:缺乏整合素αvß6(一种转化生长因子-ß1激活因子)的线虫感染小鼠的肠上皮中异常黏膜肥大细胞蛋白酶的表达

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摘要

Infection of mice with the nematode Trichinella spiralis triggers recruitment and differentiation of intraepithelial intestinal mucosal mast cells expressing mouse mast cell protease 1 (Mcpt-1), which contributes to expulsion of the parasite. Expression of Mcpt-1 is transforming growth factor (TGF)-ß1-dependent in vitro. TGF-ß1, which is secreted within tissues as a biologically inactive complex with latency-associated peptide, requires extracellular modification to become functionally active. The integrin-ß6 mediates local activation of TGF-ß1 in association with epithelia. Using T. spiralis-infected ß6–/– mice, we show accumulation of mucosal mast cells in the lamina propria of the small intestine with minimal recruitment into the epithelial compartment. This was accompanied by a coordinate reduction in expression of both Mcpt-1 and -2 in the jejunum and increased tryptase expression, whereas Mcpt-9 became completely undetectable. In contrast, the cytokine stem cell factor, a regulator of mast cell differentiation and survival, was significantly up-regulated in T. spiralis-infected ß6–/– mice compared with infected ß6+/+ controls. Despite these changes, ß6–/– mice still appeared to expel the worms normally. We postulate that compromised TGF-ß1 activation within the gastrointestinal epithelial compartment is a major, but not the only, contributing factor to the observed changes in mucosal mast cell protease and epithelial cytokine expression in ß6–/– mice.
机译:用线虫旋毛虫​​感染小鼠会触发表达小鼠肥大细胞蛋白酶1(Mcpt-1)的上皮内肠粘膜肥大细胞的募集和分化,这有助于驱除寄生虫。 Mcpt-1的表达在体外是转化生长因子(TGF)-ß1依赖性的。 TGF-ß1以与潜伏期相关的肽作为生物惰性复合物在组织内分泌,需要进行细胞外修饰才能发挥功能。整合素β6介导与上皮细胞有关的TGF-β1的局部活化。使用经螺旋藻感染的ß6-/-小鼠,我们显示了小肠固有层中粘膜肥大细胞的积累,而向上皮区室的募集最少。这伴随着空肠中Mctt-1和-2表达的坐标降低和类胰蛋白酶表达的增加,而Mcpt-9变得完全不可检测。相比之下,螺旋菌感染的ß6-/-小鼠与肥大的ß6+ / +对照相比,细胞因子干细胞因子(肥大细胞分化和存活的调节剂)显着上调。尽管有这些变化,ß6-/ –小鼠仍似乎可以正常驱除蠕虫。我们推测,胃肠道上皮区室中TGF-β1激活受损是主要的,但不是唯一的,是观察到的ß6-/-小鼠黏膜肥大细胞蛋白酶和上皮细胞因子表达变化的因素。

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