摘要
目的构建DNA修饰的胶原(DNA-Col)支架,探究改性后胶原(Col)生物相容性与促口腔黏膜软组织缺损愈合的性能。方法通过将Col材料浸泡于含DNA和磷酸基团活化剂的缓冲液中进行化学交联,以此构建出DNA-Col。通过甲基绿染色对DNA-Col上交联的DNA进行表征,并进一步利用衰减全反射-傅里叶变换红外光谱对DNA与Col的交联机制进行初步探索。之后,利用扫描电镜观察DNA-Col的表面形貌。在评价DNA-Col的生物相容性方面,采用了溶血实验、CCK-8细胞增殖实验和活/死细胞染色实验。随后在体外将DNA-Col与人口腔成纤维细胞共培养,通过qRT-PCR检测转化生长因子-β(TGF-β)、成纤维细胞生长因子-1(FGF-1)的mRNA表达水平,分析DNA-Col促进口腔黏膜缺损愈合的潜力。最后,在大鼠腭部黏膜缺损模型中检测DNA-Col的促愈合能力,并于术后10 d对各组黏膜愈合情况进行组织切片分析。结果DNA-Col保持了Col的特征性结构且生物相容性良好。人口腔成纤维细胞与DNA-Col共培养后,TGF-β、FGF-1等与细胞增殖迁移相关基因表达显著升高,提示DNA-Col具有促口腔黏膜愈合的潜力。大鼠腭部黏膜缺损模型显示DNA-Col组在术后10 d时创面愈合率可达(97.04±2.07)%,显著高于普通Col组[(79.38±5.76)%,P<0.01]。结论DNA-Col具有良好的生物相容性以及促口腔黏膜软组织缺损愈合的性能。
Objective To construct a DNA-modified collagen(DNA-Col)scaffold to investigate the biocompatibility of the modified collagen(Col)and its performance in promoting the healing of oral mucosal soft tissue defects.Methods DNA-Col was constructed by chemical cross-linking methods by soaking Col materials in a buffer containing DNA and phosphate group activators.DNA crosslinked on DNA-Col was characterized by methyl green staining,and the cross-linking mechanism between DNA and Col was preliminarily explored by attenuated total reflection-Fourier transform infrared spectroscopy.The surface morphology of DNA-Col was observed by scanning electron microscopy.The biocompatibility of DNA-Col was evaluated by hemolysis test,CCK-8 cell proliferation assay and live/dead staining test.DNA-Col was then co-cultured with human oral fibroblasts in vitro,and the mRNA expression levels of transforming growth factor-β(TGF-β)and fibroblast growth factor-1(FGF-1)were detected by qRT-PCR,so as to analyze the potential of DNA-Col in promoting the healing of oral mucosal defects.Finally,the healing ability of DNA-Col was detected in the rat palatal mucosal defect model,and the mucosal healing of each group was analyzed by tissue sections 10 d after surgery.Results DNA-Col maintained the characteristic structure of Col and exhibited good biocompatibility.After co-culture of human oral fibroblasts with DNA-Col,the expressions of TGF-β,FGF-1 and other genes related to cell proliferation and migration were significantly increased,indicating that DNA-Col has the potential to promote oral mucosal healing.The rat palatal mucosal defect model showed that the wound healing rate of DNA-Col group was(97.04±2.07)%at 10 d after surgery,which was significantly higher than that of Col group[(79.38±5.76)%,P<0.01].Conclusion DNA-Col exhibits excellent biocompatibility and has the ability to promote the healing of oral mucosal soft tissue defects.
作者
党高鹏
汪亦菲
王雨竹
宋婧涵
白鹊
李之婷
牛丽娜
顾俊婷
DANG Gaopeng;WANG Yifei;WANG Yuzhu;SONG Jinghan;BAI Que;LI Zhiting;NIU Li'na;GU Junting(State Key Laboratory of Oral&Maxillofacial Reconstruction and Regeneration,National Clinical Research Center for Oral Diseases,Shaanxi Key Laboratory of Stomatology,Department of Prosthodontics,School of Stomatology,Air Force Medical University,Xi'an 710032,China;Stomatology Center,Taihe Hospital,Hubei University of Medicine,Shiyan 442000,China)
出处
《空军军医大学学报》
CAS
2024年第10期1104-1109,共6页
Journal of Air Force Medical University
基金
国家自然科学基金(82325012,82301043)
国家口腔疾病临床研究中心资助课题计划项目(LCA202004)
国家资助博士后研究人员计划项目(GZC20233582)
陕西省科协青年人才托举计划项目(20240304)
陕西省创新能力支撑计划项目(2020TD-033)。
关键词
胶原支架
DNA
口腔黏膜
软组织增量
生物相容性
collagen scaffold
DNA
oral mucosa
soft tissue augmentation
biocompatibility