Ma Chunli, Li Yixiao, Liu Baoling, Deng Junjie, Gao Xue, Zhang Huixin, Zhang Bingqiang, Zhou Qihui, Peng Xiaoting, Zhang Han
Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250021, China; Shandong First Medical University & Shandong Academy of Medical Science, Jinan 271016, China; Qingdao Key Laboratory of Materials for Tissue Repair and Rehabilitation, Shandong Engineering Research Center for Tissue Rehabilitation Materials and Devices, School of Rehabilitation Sciences and Engineering, University of Health and Rehabilitation Sciences, Qingdao 266113, China.
Shandong First Medical University & Shandong Academy of Medical Science, Jinan 271016, China; Shandong University, Jinan 250100, China.
Colloids Surf B Biointerfaces. 2025 Mar;247:114454. doi: 10.1016/j.colsurfb.2024.114454. Epub 2024 Dec 12.
In the corneal wound healing process, epithelial cell re-epithelialization and migration are the critical first steps following an injury. As the disease progresses, orderly regeneration of corneal stromal collagen and mild corneal stromal fibrosis are vital for corneal function reconstruction. Exosomes derived from adipose-derived mesenchymal stem cells (ADSCs-Exos) have emerged as a promising therapy due to their anti-oxidant, anti-apoptosis, and tissue repair properties. In this study, we successfully isolated exosomes via differential centrifugation and verified their effective extraction through transmission electron microscopy and nanoparticle tracking analysis. In vitro, ADSCs-Exos increased corneal epithelial cell migration by 20 % and reduced oxidative damage by 50 %. In addition, ADSCs-Exos demonstrated remarkable wound healing properties in corneal tissue. This effect was attributed to their ability to inhibit apoptosis of corneal stroma cells by upregulating Bax and downregulating Bcl2, reducing the Bax/Bcl2 protein expression ratio from 1 to 0.45. This decrease may subsequently inhibit α-SMA expression, thereby preventing corneal scarring. Overall, this research has elucidated the effects and potential targets of ADSCs-Exos in promoting corneal wound repair, offering a novel and promising approach for treating corneal injuries.
在角膜伤口愈合过程中,上皮细胞重新上皮化和迁移是受伤后的关键首要步骤。随着疾病进展,角膜基质胶原蛋白的有序再生和轻度角膜基质纤维化对于角膜功能重建至关重要。源自脂肪间充质干细胞的外泌体(ADSCs-Exos)因其抗氧化、抗凋亡和组织修复特性而成为一种有前景的治疗方法。在本研究中,我们通过差速离心成功分离出外泌体,并通过透射电子显微镜和纳米颗粒跟踪分析验证了其有效提取。在体外,ADSCs-Exos使角膜上皮细胞迁移增加20%,并使氧化损伤降低50%。此外,ADSCs-Exos在角膜组织中表现出显著的伤口愈合特性。这种作用归因于它们通过上调Bax和下调Bcl2来抑制角膜基质细胞凋亡的能力,使Bax/Bcl2蛋白表达比率从1降至0.45。这种降低随后可能抑制α-SMA表达,从而防止角膜瘢痕形成。总体而言,本研究阐明了ADSCs-Exos在促进角膜伤口修复中的作用及潜在靶点,为治疗角膜损伤提供了一种新颖且有前景的方法。