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由表皮生长因子和重组类人胶原蛋白组成的混合冻干敷料可促进大鼠皮肤伤口愈合。

Hybrid Freeze-Dried Dressings Composed of Epidermal Growth Factor and Recombinant Human-Like Collagen Enhance Cutaneous Wound Healing in Rats.

作者信息

Cheng Yating, Li Yangfan, Huang Shiyi, Yu Fenglin, Bei Yu, Zhang Yifan, Tang Jianzhong, Huang Yadong, Xiang Qi

机构信息

Institute of Biomedicine and Guangdong Provincial Key Laboratory of Bioengineering Medicine, Jinan University, Guangzhou, China.

Biopharmaceutical R&D Center of Jinan University, Guangzhou, China.

出版信息

Front Bioeng Biotechnol. 2020 Jul 15;8:742. doi: 10.3389/fbioe.2020.00742. eCollection 2020.

DOI:10.3389/fbioe.2020.00742
PMID:32760705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7375021/
Abstract

Epidermal growth factor (EGF) is important for promoting skin repair and remodeling. Native collagen is also widely used as a scaffold for skin tissue engineering. The limitations of EGF include easy decomposition or inactivation, whereas native collagen is immunogenic and has poor solubility. Therefore, we constructed a freeze-dried dressing based on the recombinant human-like collagen (RHC) to act as a carrier for EGF (RHC/EGF freeze-dried dressing) and promote skin wound closure. Here, the freeze-dried dressing that combined EGF and RHC significantly enhanced the proliferation, adhesion, and spreading of NIH/3T3 fibroblasts and migration of HaCaT keratinocytes at the wound site. The physicochemical characteristics of the RHC/EGF freeze-dried dressing investigated using scanning electron microscopy, Fourier transform infrared (FTIR) spectroscopy, and differential scanning calorimetry revealed that it was a loose and porous cake that redissolved quickly. The molecular mechanisms involved in cell proliferation and angiogenesis were also assessed. The expression levels of the markers Ki-67, proliferating cell nuclear antigen, vascular endothelial growth factor, and cluster of differentiation 31 were significantly increased after treatment with the RHC/EGF freeze-dried dressing ( < 0.01, vs. RHC or EGF alone). This increase indicated that the RHC/EGF freeze-dried dressing significantly accelerated wound closure, re-epithelialization, and the orderly arrangement and deposition of collagen in the Sprague-Dawley rats with full-thickness skin defects. This work describes a significant step toward the development of wound environments conducive to healing, and the RHC/EGF freeze-dried dressing is a potential therapeutic strategy in wound management.

摘要

表皮生长因子(EGF)对促进皮肤修复和重塑很重要。天然胶原蛋白也被广泛用作皮肤组织工程的支架。EGF的局限性包括容易分解或失活,而天然胶原蛋白具有免疫原性且溶解性差。因此,我们构建了一种基于重组类人胶原蛋白(RHC)的冻干敷料,作为EGF的载体(RHC/EGF冻干敷料),以促进皮肤伤口愈合。在此,结合了EGF和RHC的冻干敷料显著增强了NIH/3T3成纤维细胞的增殖、黏附、铺展以及伤口部位HaCaT角质形成细胞的迁移。使用扫描电子显微镜、傅里叶变换红外(FTIR)光谱和差示扫描量热法对RHC/EGF冻干敷料的理化特性进行研究,结果表明它是一种疏松多孔的块状物,能快速重新溶解。还评估了细胞增殖和血管生成所涉及的分子机制。用RHC/EGF冻干敷料处理后,标记物Ki-67、增殖细胞核抗原、血管内皮生长因子和分化簇31的表达水平显著升高(与单独使用RHC或EGF相比,<0.01)。这种升高表明RHC/EGF冻干敷料显著加速了具有全层皮肤缺损的Sprague-Dawley大鼠的伤口愈合、再上皮化以及胶原蛋白的有序排列和沉积。这项工作朝着开发有利于愈合的伤口环境迈出了重要一步,并且RHC/EGF冻干敷料是伤口管理中的一种潜在治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/a4a6035ef34a/fbioe-08-00742-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/8033433bd276/fbioe-08-00742-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/2d4788550293/fbioe-08-00742-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/120f1f986249/fbioe-08-00742-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/2775987afdf5/fbioe-08-00742-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/986fce5fa3e2/fbioe-08-00742-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/a4a6035ef34a/fbioe-08-00742-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/8033433bd276/fbioe-08-00742-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/2d4788550293/fbioe-08-00742-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/120f1f986249/fbioe-08-00742-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/2775987afdf5/fbioe-08-00742-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/986fce5fa3e2/fbioe-08-00742-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18da/7375021/a4a6035ef34a/fbioe-08-00742-g006.jpg

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