首页> 外文期刊>Virology >Increased gelatinase B/matrix metalloproteinase 9 (MMP-9) activity in a murine model of acute coxsackievirus B4-induced pancreatitis.
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Increased gelatinase B/matrix metalloproteinase 9 (MMP-9) activity in a murine model of acute coxsackievirus B4-induced pancreatitis.

机译:在急性柯萨奇病毒B4诱发的胰腺炎小鼠模型中,明胶酶B /基质金属蛋白酶9(MMP-9)活性增加。

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摘要

Infection of mice with coxsackievirus B4 results within days in a severe acute necrotizing pancreatitis, which resolves completely within weeks. Gelatinase B or matrix metalloproteinase 9 (MMP-9) has previously been shown to be involved in several models of pancreatitis, but its role in virus-induced pancreatitis has never been investigated. We here report that MMP-9 levels are markedly increased in the pancreas of mice that developed acute pancreatitis following infection with coxsackievirus B4. Moreover, using in situ zymography, we demonstrated that MMP-9 is active in vivo. Double immunohistochemical analysis revealed that macrophages and neutrophils were the cellular source of MMP-9. Extensive tissue rearrangements involving collagen turnover were observed, and these were associated with extensive pathology and resolution of the disease. In summary, this report demonstrates that acute coxsackievirus B4-induced pancreatitis involves the action of MMP-9, which is mainly originating from macrophages and neutrophils.
机译:柯萨奇病毒B4感染小鼠会在数天内导致严重的急性坏死性胰腺炎,并在数周内完全消退。明胶酶B或基质金属蛋白酶9(MMP-9)先前已被证明参与多种胰腺炎模型,但从未研究过其在病毒性胰腺炎中的作用。我们在此报告,柯萨奇病毒B4感染后发展为急性胰腺炎的小鼠胰腺中MMP-9水平显着增加。此外,使用原位酶谱,我们证明了MMP-9在体内具有活性。双重免疫组织化学分析显示巨噬细胞和嗜中性粒细胞是MMP-9的细胞来源。观察到涉及胶原转换的广泛组织重排,这些与广泛的病理学和疾病的解决有关。总而言之,该报告表明急性柯萨奇病毒B4诱发的胰腺炎涉及MMP-9的作用,该作用主要源自巨噬细胞和嗜中性粒细胞。

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