Song Congjing, Wang Hui, Huang Feifei, Li Sijia, Li Ming, Deng Wanying, Chen Weiqiang
School of Basic Medical Sciences, Guangdong Pharmaceutical University, Guangzhou 510006, China; School of Nursing, Guangdong Pharmaceutical University, Guangzhou 510006, China.
School of Basic Medical Sciences, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Int J Biol Macromol. 2025 Mar;292:139221. doi: 10.1016/j.ijbiomac.2024.139221. Epub 2024 Dec 29.
The self-assembled peptide RADA16-I (RADARADARADARADA) has been widely used in biomaterials. However, studies on the practical application of self-assembled peptide hydrogels loaded with bioactive peptides are still insufficient. In this study, we successfully prepared the peptide nanofiber gel RGJ by incorporating the bioactive peptides A8SGLP-1 (G) and Jagged-1 (J) into RADA16-I (R) in specific ratios. The mechanical properties, secondary structure, and microstructure of RGJ were thoroughly characterized using a rheometer, circular dichroism (CD), and transmission electron microscopy (TEM). The results showed that R and RGJ adopted stable β-folded structures at room temperature, and RGJ exhibited a nanofiber mesh structure, confirming its excellent physical properties. Cellular experiments demonstrated that RGJ significantly enhanced the proliferation and migration of HaCaT, L929, and HUVEC cells, with the most pronounced effect observed in HUVEC cells. In the 100 μg/mL RGJ-treated group, cell viability (OD value) reached 1.369, which was significantly higher than that of the control group (0.673) and the R-only group (0.848). The strongest pro-migratory effect was observed in HaCaT cells, with a scratch closure rate of 22.83 %. In vivo experiments showed that the deep second-degree burn wounds of mice in the RGJ gel-treated group healed rapidly by day 17, exhibiting 99.5 % wound closure, compared to 84.02 % in the R gel group, and 73.02 % and 70.97 % in the control and burn cream groups, respectively. Immunohistochemistry and ELISA results further confirmed that RGJ significantly reduced wound and systemic inflammatory responses while promoting the secretion of pro-angiogenic factors VEGF and CD31, revealing its potential mechanism for enhancing burn wound healing. Additionally, RGJ significantly reduced wound scar formation and increased skin collagen deposition, demonstrating a favorable biosafety profile compared to the control group, commercial burn ointment, and the R-only treatment group. In conclusion, the development of the peptide nanofiber gel RGJ holds great potential for wound management applications and lays a foundation for future related research.
自组装肽RADA16-I(RADARADARADARADA)已在生物材料中得到广泛应用。然而,关于负载生物活性肽的自组装肽水凝胶实际应用的研究仍不充分。在本研究中,我们通过将生物活性肽A8SGLP-1(G)和Jagged-1(J)以特定比例掺入RADA16-I(R)中,成功制备了肽纳米纤维凝胶RGJ。使用流变仪、圆二色光谱(CD)和透射电子显微镜(TEM)对RGJ的力学性能、二级结构和微观结构进行了全面表征。结果表明,R和RGJ在室温下均采用稳定的β折叠结构,且RGJ呈现出纳米纤维网状结构,证实了其优异的物理性能。细胞实验表明,RGJ显著增强了HaCaT、L929和HUVEC细胞的增殖和迁移能力,其中对HUVEC细胞的影响最为显著。在100μg/mL RGJ处理组中,细胞活力(OD值)达到1.369,显著高于对照组(0.673)和仅含R的组(0.848)。在HaCaT细胞中观察到最强的促迁移作用,划痕闭合率为22.83%。体内实验表明,RGJ凝胶处理组小鼠的深二度烧伤创面在第17天迅速愈合,创面闭合率达99.5%,相比之下,R凝胶组为84.02%,对照组和烧伤膏组分别为73.02%和70.97%。免疫组织化学和ELISA结果进一步证实,RGJ在促进促血管生成因子VEGF和CD31分泌的同时,显著降低了创面和全身的炎症反应,揭示了其促进烧伤创面愈合的潜在机制。此外,RGJ显著减少了创面瘢痕形成并增加了皮肤胶原沉积,与对照组、市售烧伤软膏和仅含R的治疗组相比,显示出良好的生物安全性。总之,肽纳米纤维凝胶RGJ的开发在伤口管理应用方面具有巨大潜力,并为未来相关研究奠定了基础。