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载银纳米粒子胶原/壳聚糖支架通过调控成纤维细胞迁移和巨噬细胞活化促进创面愈合。

Silver nanoparticle loaded collagen/chitosan scaffolds promote wound healing via regulating fibroblast migration and macrophage activation.

机构信息

Department of Burns & Wound Care Center, Second Affiliated Hospital of Medical College, Zhejiang University, Hangzhou, 310009, China.

出版信息

Sci Rep. 2017 Sep 5;7(1):10489. doi: 10.1038/s41598-017-10481-0.

DOI:10.1038/s41598-017-10481-0
PMID:28874692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5585259/
Abstract

Treatment of full-thickness skin defects poses significant clinical challenges including risk of infection and severe scaring. Silver nanoparticle (NAg), an effective antimicrobial agent, has provided a promising therapeutic method for burn wounds. However, the detailed mechanism remains unknown. Hence, we constructed a metallic nanosilver particles-collagen/chitosan hybrid scaffold (NAg-CCS) and investigated its potential effects on wound healing. In vitro scratch assay, immunofluorescence staining and antibacterial activity of the scaffold were all studied. In vivo NAg-CCS was applied in full-thickness skin defects in Sprague-Dawley (SD) rats and the therapeutic effects of treatment were evaluated. The results showed that NAg at a concentration of 10 ppm accelerated the migration of fibroblasts with an increase in expression of α-smooth muscle actin (α-SMA). Furthermore, in vivo studies showed increased levels of pro-inflammatory and scar-related factors as well as α-SMA, while markers for macrophage activation were up-regulated. On day 60 post transplantation of ultra-thin skin graft, the regenerated skin by NAg-CCS had a similar structure to normal skin. In summary, we demonstrated that NAg-CCS was bactericidal, anti-inflammatory and promoted wound healing potentially by regulating fibroblast migration and macrophage activation, making it an ideal dermal substitute for wound regeneration.

摘要

全层皮肤缺损的治疗存在重大的临床挑战,包括感染和严重瘢痕的风险。纳米银(NAg)作为一种有效的抗菌剂,为烧伤创面提供了一种有前途的治疗方法。然而,其详细机制尚不清楚。因此,我们构建了一种金属纳米银颗粒-胶原/壳聚糖杂化支架(NAg-CCS),并研究了其在伤口愈合中的潜在作用。研究了支架的体外划痕试验、免疫荧光染色和抗菌活性。将 NAg-CCS 应用于 Sprague-Dawley(SD)大鼠的全层皮肤缺损,并评估其治疗效果。结果表明,浓度为 10ppm 的 NAg 可促进成纤维细胞的迁移,增加α-平滑肌肌动蛋白(α-SMA)的表达。此外,体内研究表明,促炎和瘢痕相关因子以及α-SMA 的水平升高,而巨噬细胞激活的标志物上调。在超薄皮片移植后 60 天,NAg-CCS 再生的皮肤具有与正常皮肤相似的结构。总之,我们证明了 NAg-CCS 具有杀菌、抗炎作用,并通过调节成纤维细胞迁移和巨噬细胞激活促进伤口愈合,使其成为一种理想的用于创面再生的真皮替代物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/8e1074b1906a/41598_2017_10481_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/3406a751b829/41598_2017_10481_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/feae7c8cd0ee/41598_2017_10481_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/334ed42ad312/41598_2017_10481_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/a246890f0c96/41598_2017_10481_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/e353b841b906/41598_2017_10481_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/83276c73dbe9/41598_2017_10481_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/8a104c5c4145/41598_2017_10481_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/87d2f4ae683a/41598_2017_10481_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/8e1074b1906a/41598_2017_10481_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/3406a751b829/41598_2017_10481_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/feae7c8cd0ee/41598_2017_10481_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/334ed42ad312/41598_2017_10481_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/a246890f0c96/41598_2017_10481_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/e353b841b906/41598_2017_10481_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/83276c73dbe9/41598_2017_10481_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/8a104c5c4145/41598_2017_10481_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/87d2f4ae683a/41598_2017_10481_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d5/5585259/8e1074b1906a/41598_2017_10481_Fig9_HTML.jpg

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