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诱导多能干细胞衍生的微囊泡通过 miR-16-5p 介导促进角质形成细胞迁移加速小鼠深二度烧伤创面愈合。

Induced pluripotent stem cells-derived microvesicles accelerate deep second-degree burn wound healing in mice through miR-16-5p-mediated promotion of keratinocytes migration.

机构信息

Department of Histology and Embryology, School of Basic Medical Science, Southern Medical University, Guangzhou 510515, China.

Guangdong Provincial Key Laboratory of Construction and Detection in Tissue Engineering, Guangzhou 510515, China.

出版信息

Theranostics. 2020 Aug 8;10(22):9970-9983. doi: 10.7150/thno.46639. eCollection 2020.

Abstract

Induced pluripotent stem cells (iPSCs) have emerged as a promising treatment paradigm for skin wounds. Extracellular vesicles are now recognized as key mediators of beneficial stem cells paracrine effects. In this study, we investigated the effect of iPSCs-derived microvesicles (iPSCs-MVs) on deep second-degree burn wound healing and explored the underlying mechanism. iPSCs-MVs were isolated and purified from conditioned medium of iPSCs and confirmed by electron micrograph and size distribution. In deep second-degree burn model, iPSCs-MVs were injected subcutaneously around wound sites and the efficacy was assessed by measuring wound closure areas, histological examination and immunohistochemistry staining. , CCK-8, EdU staining and scratch assays were used to assess the effects of iPSCs-MVs on proliferation and migration of keratinocytes. Next, we explored the underlying mechanisms by high-throughput microRNA sequencing. The roles of the miR-16-5p in regulation of keratinocytes function induced by iPSCs-MVs were assessed. Moreover, the target gene which mediated the biological effects of miR-16-5p in keratinocytes was also been detected. Finally, we examined the effect of local miR-16-5p treatment on deep second degree-burns wound healing in mice. The local transplantation of iPSCs-MVs into the burn wound bed resulted in accelerated wound closure including the increased re-epithelialization. , iPSCs-MVs could promote the migration of keratinocytes. We also found that miR-16-5p is a critical factor in iPSCs-MVs-induced promotion of keratinocytes migration through activating p38/MARK pathway by targeting Desmoglein 3 (Dsg3). Finally, we confirmed that local miR-16-5p treatment could boost re-epithelialization during burn wound healing. Therefore, our results indicate that iPSCs-MVs-derived miR-16-5p may be a novel therapeutic approach for deep second-degree burn wound healing.

摘要

诱导多能干细胞 (iPSCs) 已成为治疗皮肤创伤的一种很有前途的治疗方法。细胞外囊泡现在被认为是有益的干细胞旁分泌作用的关键介质。在这项研究中,我们研究了 iPSCs 衍生的微泡 (iPSCs-MVs) 对深二度烧伤创面愈合的影响,并探讨了其潜在机制。iPSCs-MVs 从 iPSCs 的条件培养基中分离和纯化,并通过电子显微镜和粒径分布进行确认。在深二度烧伤模型中,将 iPSCs-MVs 注射到伤口周围的皮下组织中,并通过测量伤口闭合面积、组织学检查和免疫组织化学染色来评估疗效。此外,我们还通过高通量 microRNA 测序来探讨潜在机制。通过 CCK-8、EdU 染色和划痕实验来评估 iPSCs-MVs 对角质形成细胞增殖和迁移的影响。接下来,我们评估了 miR-16-5p 在调节 iPSCs-MVs 诱导的角质形成细胞功能中的作用。此外,还检测了介导 miR-16-5p 在角质形成细胞中生物学效应的靶基因。最后,我们检测了局部 miR-16-5p 治疗对深二度烧伤创面愈合的影响。将 iPSCs-MVs 局部移植到烧伤创面床可加速创面闭合,包括增加再上皮化。此外,iPSCs-MVs 可促进角质形成细胞迁移。我们还发现,miR-16-5p 是 iPSCs-MVs 诱导角质形成细胞迁移的关键因素,通过靶向桥粒芯糖蛋白 3 (Dsg3) 激活 p38/MARK 通路。最后,我们证实局部 miR-16-5p 治疗可促进烧伤创面愈合过程中的再上皮化。因此,我们的结果表明,iPSCs-MVs 衍生的 miR-16-5p 可能是治疗深二度烧伤创面愈合的一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51e8/7481429/22ca39320489/thnov10p9970g001.jpg

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