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低聚果糖诱导马属动物蹄叶炎发展过程中的板层白细胞浸润及白细胞介素-6的参与

Lamellar leukocyte infiltration and involvement of IL-6 during oligofructose-induced equine laminitis development.

作者信息

Visser Michelle B, Pollitt Christopher C

机构信息

The Australian Equine Laminitis Research Unit, School of Veterinary Science, The University of Queensland, Gatton 4343, Australia.

出版信息

Vet Immunol Immunopathol. 2011 Nov 15;144(1-2):120-8. doi: 10.1016/j.vetimm.2011.07.016. Epub 2011 Jul 26.

Abstract

Laminitis is known to involve deregulation of proteases and destruction of the lamellar basement membrane with the host inflammatory response also playing a role. Leukocyte infiltration has been well characterized in the black walnut model of laminitis induction, but not in carbohydrate induced models. Increased gene expression of multiple cytokines, including IL-6, has also been implicated in laminitis development. Using real time PCR, immunohistochemistry and zymography methods, we characterize leukocyte infiltration and IL-6 gene expression in oligofructose (OF) induced laminitis. As well, we use two in vitro models to investigate a role for IL-6 in protease regulation. Laminitis was induced in normal standardbred horses (n=5) by alimentary OF dosing and lamellar biopsies were obtained throughout the 48 h experimental period. Lamellar explants and keratinocytes were also isolated from clinically normal horses for in vitro experiments. We found infiltration of calprotectin-positive leukocytes (monocytes and neutrophils) at 18-24h post oligofructose dosing, while IL-6 gene expression was increased as early as 12h post dosing. Additionally, while we found that IL-6 did not cause significant BM damage in vitro, it did result in increased secreted proMMP-9 levels from lamellar explants. Thus, we find that leukocyte infiltration does occur during oligofructose-induced laminitis development, however, IL-6 gene expression in the lamellae may precede leukocyte infiltration. Additionally, we show IL-6 plays a role in increasing the level of proMMP-9 in vivo in a manner that does not involve keratinocytes.

摘要

已知蹄叶炎涉及蛋白酶失调和板层基底膜破坏,宿主炎症反应也起作用。在黑胡桃诱导蹄叶炎模型中,白细胞浸润已得到充分表征,但在碳水化合物诱导模型中尚未得到充分表征。包括白细胞介素-6(IL-6)在内的多种细胞因子基因表达增加也与蹄叶炎发展有关。我们使用实时聚合酶链反应(PCR)、免疫组织化学和酶谱分析方法,对低聚果糖(OF)诱导的蹄叶炎中的白细胞浸润和IL-6基因表达进行表征。此外,我们使用两种体外模型研究IL-6在蛋白酶调节中的作用。通过经口给予OF在正常标准马(n = 5)中诱导蹄叶炎,并在整个48小时实验期内获取板层活检样本。还从临床正常马中分离出板层外植体和角质形成细胞用于体外实验。我们发现,在给予低聚果糖后18 - 24小时,钙卫蛋白阳性白细胞(单核细胞和中性粒细胞)浸润,而IL-6基因表达在给药后12小时就已增加。此外,虽然我们发现IL-6在体外不会导致显著的基底膜损伤,但它确实导致板层外植体分泌的前基质金属蛋白酶-9(proMMP-9)水平增加。因此,我们发现在低聚果糖诱导的蹄叶炎发展过程中确实发生了白细胞浸润,然而,板层中IL-6基因表达可能先于白细胞浸润。此外,我们表明IL-6在体内以不涉及角质形成细胞的方式在增加proMMP-9水平方面发挥作用。

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