Ha Sang Su, Song Eui Sun, Du Ping, Suhaeri Muhammad, Lee Jong Ho, Park Kwideok
Center for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
Division of Bio-Medical Science and Technology, KIST School, University of Science and Technology (UST), Seoul 02792, Republic of Korea.
ACS Biomater Sci Eng. 2020 Jul 13;6(7):4266-4275. doi: 10.1021/acsbiomaterials.0c00657. Epub 2020 Jun 22.
Decellularized extracellular matrix (ECM)-based scaffold has been a very useful resource for effective tissue regeneration. In this study, we report a novel ECM patch that physically combines human fibroblast-derived matrix (hFDM) and poly(vinyl alcohol) (PVA) hydrogel. hFDM was obtained after decellularization of cultured human fibroblasts. We investigated the basic characteristics of hFDM alone using immunofluorescence (fibronectin, collagen type I) and angiogenesis-related factor analysis. Successful incorporation of hFDM with PVA produced an hFDM/PVA patch, which showed excellent cytocompatibility with human mesenchymal stem cells (hMSCs), as assessed via cell adhesion, viability, and proliferation. Moreover, scratch assay using human dermal fibroblasts showed a significant improvement of cell migration when treated with the paracrine factors originated from the hMSC-incorporated hFDM. To evaluate the therapeutic effect on wound healing, hMSCs were seeded on the hFDM/PVA patch and they were then transplanted into a mouse full-thickness wound model. Among four experimental groups (control, PVA, hFDM/PVA, hMSC/hFDM/PVA), we found that hMSC/hFDM/PVA patch accelerated the wound closure with time. More notably, histology and immunofluorescence demonstrated that compared to the other interventions tested, hMSC/hFDM/PVA patch could lead to significantly advanced tissue regeneration, as confirmed via nearly normal epidermis thickness, skin adnexa regeneration (hair follicle), mature collagen deposition, and neovascularization. Additionally, cell tracking of prelabeled hMSCs suggests the retention of transplanted cells in the wound region after the transplantation of hMSC/hFDM/PVA patch. Taken together, our engineered ECM patch supports a strong regenerative potential toward advanced wound healing.
基于脱细胞细胞外基质(ECM)的支架一直是有效组织再生的非常有用的资源。在本研究中,我们报告了一种新型的ECM贴片,它将人成纤维细胞衍生基质(hFDM)和聚乙烯醇(PVA)水凝胶物理结合在一起。hFDM是在培养的人成纤维细胞脱细胞后获得的。我们使用免疫荧光(纤连蛋白、I型胶原蛋白)和血管生成相关因子分析研究了单独的hFDM的基本特性。hFDM与PVA成功结合产生了hFDM/PVA贴片,通过细胞黏附、活力和增殖评估,该贴片与人骨髓间充质干细胞(hMSCs)具有优异的细胞相容性。此外,使用人皮肤成纤维细胞的划痕试验表明,用源自hMSC掺入的hFDM的旁分泌因子处理时,细胞迁移有显著改善。为了评估对伤口愈合的治疗效果,将hMSCs接种在hFDM/PVA贴片上,然后将它们移植到小鼠全层伤口模型中。在四个实验组(对照组、PVA组、hFDM/PVA组、hMSC/hFDM/PVA组)中,我们发现hMSC/hFDM/PVA贴片随时间加速了伤口闭合。更值得注意的是,组织学和免疫荧光表明,与其他测试干预措施相比,hMSC/hFDM/PVA贴片可导致显著的组织再生进展,这通过几乎正常的表皮厚度、皮肤附属器再生(毛囊)、成熟胶原蛋白沉积和新血管形成得到证实。此外,对预先标记的hMSCs的细胞追踪表明,在移植hMSC/hFDM/PVA贴片后,移植细胞保留在伤口区域。综上所述,我们设计的ECM贴片对促进伤口愈合具有强大的再生潜力。