Zhan Guancheng, Yu Lixia, Wang Qiqi, Jin Longyang, Yin Xiaohong, Cao Xiaodong, Gao Huichang
School of Medicine, South China University of Technology, Guangzhou 510006, People's Republic of China.
Department of Gastrointestinal Surgery, The Sixth Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510655, People's Republic of China.
Biomed Mater. 2024 Mar 8;19(3). doi: 10.1088/1748-605X/ad2ed2.
Corneal stromal injury is a common surgical disease. With the development of tissue engineering materials, many artificial corneal scaffolds have been developed to replace allograft corneal transplantation and solve the problem of corneal donor shortage. However, few researchers have paid attention to corneal stromal wound healing. Herein, a nanocomposite of amino modified mesoporous bioactive glass (MBG-NH) and microRNA-133b (miR-133b) was introduced into the patterned collagen films to achieve corneal stromal injury repair. MBG-NHnanoparticles as a nano delivery carrier could efficiently load miR-133b and achieve the slow release of miR-133b. The physicochemical properties of collagen films were characterized and found the microgrooved collagen films loaded with miR-133b@MBG-NHnanoparticles possessed similar swelling properties, optical clarity, and biodegradability to the natural cornea.cell experiments were also conducted and proved that the patterned collagen films with miR-133b@MBG-NHpossessed good biocompatibility, and miR-133b@MBG-NHnanoparticles could be significantly uptake by rabbit corneal stromal cells (RCSCs) and have a significant impact on the orientation, proliferation, migration, and gene expression of RCSCs. More importantly, the patterned collagen films with miR-133b@MBG-NHcould effectively promote the migration of RCSCs and accelerate wound healing process, and down-regulate the expression levels of-SMA, COL-I, and CTGF genes associated with myofibroblast differentiation of corneal stromal cells, which has a potential application prospect in the repair of corneal stromal injury.
角膜基质损伤是一种常见的外科疾病。随着组织工程材料的发展,已开发出许多人工角膜支架来替代同种异体角膜移植,解决角膜供体短缺的问题。然而,很少有研究人员关注角膜基质伤口愈合。在此,将氨基修饰的介孔生物活性玻璃(MBG-NH)与微小RNA-133b(miR-133b)的纳米复合材料引入图案化胶原膜中,以实现角膜基质损伤修复。MBG-NH纳米颗粒作为纳米递送载体可有效负载miR-133b并实现miR-133b的缓释。对胶原膜的物理化学性质进行了表征,发现负载有miR-133b@MBG-NH纳米颗粒的微槽胶原膜具有与天然角膜相似的溶胀特性、光学透明度和生物降解性。还进行了细胞实验,证明含有miR-133b@MBG-NH的图案化胶原膜具有良好的生物相容性,并且miR-133b@MBG-NH纳米颗粒可被兔角膜基质细胞(RCSCs)显著摄取,并对RCSCs的取向、增殖、迁移和基因表达产生显著影响。更重要的是,含有miR-133b@MBG-NH的图案化胶原膜可有效促进RCSCs的迁移并加速伤口愈合过程,并下调与角膜基质细胞肌成纤维细胞分化相关的α-SMA、COL-I和CTGF基因的表达水平,这在角膜基质损伤修复中具有潜在的应用前景。