首页> 美国卫生研究院文献>Oncotarget >Antimicrobial peptide Epinecidin-1 promotes complete skin regeneration of methicillin-resistant Staphylococcus aureus-infected burn wounds in a swine model
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Antimicrobial peptide Epinecidin-1 promotes complete skin regeneration of methicillin-resistant Staphylococcus aureus-infected burn wounds in a swine model

机译:抗菌肽Epinecidin-1促进猪模型中耐甲氧西林金黄色葡萄球菌感染的烧伤创面的完全皮肤再生

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摘要

This report shows that the antimicrobial peptide (AMP) Epinecidin-1 (Epi-1) efficiently heals MRSA-infected heat burn injuries and provides protection from infection in a pig model. The presence of an optimal level of Epi-1 induces cell proliferation by promoting cell cycle progression through an increase in S-phase cells. Epi-1 also induces proliferation to cover the wounded region in an in vitro cell proliferation assay using immortalized human epithelial HaCaT cells. Next, the in vivo wound healing efficiency of Epi-1 was tested in heat-burned pig skin infected with MRSA under in vivo conditions. Treatment of the injury with Epi-1 for 1 h at six hours post-infection completely healed the wound within 25 days. Conversely, the injury in the untreated control was not healed 25 days post-infection. Histological staining of wound sections with H&E showed that Epi-1 enhanced vascularization and increased epithelial activities in the wound region. Neutrophil recruitment to the wounded region in the Epi-1-treated sections was visualized by Giemsa staining. Additionally, Masson's trichrome staining of wound sections confirmed that Epi-1 enhanced extracellular collagen compound formation. The induction of sepsis-associated blood C-reactive protein (CRP) and the pro-inflammatory cytokine IL-6 in response to MRSA infection was also suppressed in pigs that received Epi-1. Taken together, the results demonstrate that the biomaterial Epi-1 heals wounds through increasing epithelial cell proliferation, vascularization, and the formation of collagen and controls MRSA infection-mediated sepsis in pigs.
机译:该报告表明,抗菌肽(AMP)的Epinecidin-1(Epi-1)可有效治愈MRSA感染的热灼伤,并在猪模型中提供免受感染的保护。最佳水平的Epi-1的存在可通过增加S期细胞来促进细胞周期进程,从而诱导细胞增殖。 Epi-1还使用永生化的人上皮HaCaT细胞在体外细胞增殖测定中诱导增殖以覆盖伤口区域。接下来,在体内条件下在感染了MRSA的热烧猪皮中测试了Epi-1的体内伤口愈合效率。感染后六小时用Epi-1处理伤口1小时,可在25天内完全治愈伤口。相反,未经处理的对照组的感染在感染后25天仍未he愈。 H&E对伤口切片进行组织学染色显示,Epi-1增强了伤口区域的血管形成并增加了上皮活动。通过吉姆萨染色观察到中性粒细胞募集到Epi-1处理的切片中的受伤区域。此外,伤口的Masson三色染色证实Epi-1增强了细胞外胶原化合物的形成。在接受Epi-1的猪中,败血症相关的血液C反应蛋白(CRP)和促炎细胞因子IL-6对MRSA感染的诱导也被抑制。综上所述,结果表明,生物材料Epi-1通过增加上皮细胞的增殖,血管化和胶原蛋白的形成来治愈伤口,并控制猪的MRSA感染介导的败血症。

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