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羊痘病毒白细胞介素-10和血管内皮生长因子-E协同作用促进小鼠皮肤伤口愈合。

Orf Virus IL-10 and VEGF-E Act Synergistically to Enhance Healing of Cutaneous Wounds in Mice.

作者信息

Wise Lyn M, Stuart Gabriella S, Jones Nicola C, Fleming Stephen B, Mercer Andrew A

机构信息

Department of Pharmacology and Toxicology, School of Biomedical Sciences, University of Otago, Dunedin 9054, New Zealand.

Department of Microbiology and Immunology, School of Biomedical Sciences, University of Otago, Dunedin 9054, New Zealand.

出版信息

J Clin Med. 2020 Apr 11;9(4):1085. doi: 10.3390/jcm9041085.

DOI:10.3390/jcm9041085
PMID:32290480
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7231296/
Abstract

Orf virus (OV) is a zoonotic parapoxvirus that causes highly proliferative skin lesions which resolve with minimal inflammation and scarring. OV encodes two immunomodulators, vascular endothelial growth factor (VEGF)-E and interleukin-10 (ovIL-10), which individually modulate skin repair and inflammation. This study examined the effects of the VEGF-E and ovIL-10 combination on healing processes in a murine wound model. Treatments with viral proteins, individually and in combination, were compared to a mammalian VEGF-A and IL-10 combination. Wound biopsies were harvested to measure re-epithelialisation and scarring (histology), inflammation, fibrosis and angiogenesis (immunofluorescence), and gene expression (quantitative polymerase chain reaction). VEGF-E and ovIL-10 showed additive effects on wound closure and re-epithelialisation, and suppressed M1 macrophage and myofibroblast infiltration, while allowing M2 macrophage recruitment. The viral combination also increased endothelial cell density and pericyte coverage, and improved collagen deposition while reducing the scar area. The mammalian combination showed equivalent effects on wound closure, re-epithelialisation and fibrosis, but did not promote blood vessel stabilisation or collagen remodeling. The combination treatments also differentially altered the expression of transforming growth factor beta isoforms, and These findings show that the OV proteins synergistically enhance skin repair, and act in a complimentary fashion to improve scar quality.

摘要

羊痘病毒(OV)是一种人畜共患的副痘病毒,可引起高度增殖性皮肤病变,愈合时炎症和瘢痕形成极少。OV编码两种免疫调节因子,即血管内皮生长因子(VEGF)-E和白细胞介素-10(ovIL-10),它们分别调节皮肤修复和炎症。本研究在小鼠伤口模型中考察了VEGF-E和ovIL-10联合使用对愈合过程的影响。将病毒蛋白单独及联合使用的治疗方法与哺乳动物VEGF-A和IL-10联合使用的方法进行比较。采集伤口活检组织以测量再上皮化和瘢痕形成(组织学)、炎症、纤维化和血管生成(免疫荧光)以及基因表达(定量聚合酶链反应)。VEGF-E和ovIL-10对伤口闭合和再上皮化显示出相加作用,并抑制M1巨噬细胞和成肌纤维细胞浸润,同时允许M2巨噬细胞募集。病毒组合还增加了内皮细胞密度和周细胞覆盖,并改善了胶原蛋白沉积,同时减小了瘢痕面积。哺乳动物组合在伤口闭合、再上皮化和纤维化方面显示出等效作用,但未促进血管稳定或胶原蛋白重塑。联合治疗还不同程度地改变了转化生长因子β亚型的表达,并且这些发现表明,OV蛋白协同增强皮肤修复,并以互补方式改善瘢痕质量。

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