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重组双人源化胶原蛋白和聚-L-乳酸抗皮肤衰老生物活性的体内评估

In Vivo Evaluation of the Anti-Skin-Ageing Bioactivity of a Recombinant Dual Humanised Collagen and Poly-L-Lactic Acid.

作者信息

Tong Mingjie, Zhou Xin, Zhong Jiongni, Qu Dengjian, Chen Wei, Chen Chun, Wang Yiting, Liu Yaoping, Li Shaochuan, Xiao Yuan, Wang Ning, Guo Chaowan, Xie Qiuling, Xiong Sheng

机构信息

Institute of Biomedicine and National Engineering Research Center of Genetic Medicine, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.

Guangzhou Huike Biotech Co., Ltd., Guangzhou 510530, China.

出版信息

Bioengineering (Basel). 2025 May 12;12(5):510. doi: 10.3390/bioengineering12050510.

Abstract

This study introduces a novel recombinant humanised collagen (DuCol) developed through codon optimisation and prokaryotic soluble expression, exhibiting exceptional biocompatibility and bioactivity. Structural integrity was confirmed via RP-HPLC, SEM, and CD spectroscopy. In vitro evaluations revealed DuCol's dose-dependent enhancement of NIH-3T3 fibroblast proliferation, adhesion, and migration. In a D-galactose-induced ageing rat model, subcutaneous implantation of DuCol showcased time-dependent anti-ageing effects. Early-stage intervention (30 days post-injection) markedly upregulated COL1A1 expression through the TGF-β/Smad3 pathway activation, outperforming poly-l-lactic acid (PLLA) in collagen deposition. Histological analysis revealed 23.4% greater dermal thickness in DuCol-treated groups compared to PLLA at 90 days. While PLLA exhibited sustained collagen stimulation beyond 90 days, DuCol exhibited superior early-phase efficacy ( < 0.001) with comparable safety profiles (no inflammatory response observed through 180-day monitoring). The combinatorial PLLA/DuCol (P&C) formulation synergistically enhanced dermal regeneration, achieving a 31.7% thicker collagen matrix than monotherapy groups. These results underscore the potential of DuCol as a novel implantable filler material for skin repair and regeneration.

摘要

本研究介绍了一种通过密码子优化和原核可溶性表达开发的新型重组人源化胶原蛋白(DuCol),其具有卓越的生物相容性和生物活性。通过反相高效液相色谱法(RP-HPLC)、扫描电子显微镜(SEM)和圆二色光谱法(CD)证实了其结构完整性。体外评估显示,DuCol对NIH-3T3成纤维细胞的增殖、黏附和迁移具有剂量依赖性增强作用。在D-半乳糖诱导的衰老大鼠模型中,皮下植入DuCol显示出时间依赖性的抗衰老效果。早期干预(注射后30天)通过激活TGF-β/Smad3途径显著上调COL1A1表达,在胶原蛋白沉积方面优于聚左旋乳酸(PLLA)。组织学分析显示,在90天时,DuCol治疗组的真皮厚度比PLLA组厚23.4%。虽然PLLA在90天后表现出持续的胶原蛋白刺激作用,但DuCol在早期疗效方面表现更优(P<0.001),且安全性相当(在180天的监测中未观察到炎症反应)。PLLA/DuCol组合配方(P&C)协同增强了真皮再生,形成的胶原蛋白基质比单一治疗组厚31.7%。这些结果强调了DuCol作为一种用于皮肤修复和再生的新型可植入填充材料的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ca/12109386/abc0c4aa0ac4/bioengineering-12-00510-g001.jpg

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