Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Clinical Biochemistry, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Cell Biochem Funct. 2023 Jun;41(4):434-449. doi: 10.1002/cbf.3793. Epub 2023 Apr 5.
Despite significant advancements in tissue engineering and regenerative medicine during the last two decades, the fabrication of proper scaffolds with appropriate cells can still be considered a critical achievement in this field. Hypoxia is a major stumbling block to chronic wound healing, which restrains tissue engineering plans because a lack of oxygen may cause cell death. This study evaluated the cocultured human keratinocytes and human adipose-derived mesenchymal stem cells (AMSCs) on a multilayer oxygen-releasing electrospun scaffold based on PU/PCL.Sodium percarbonate (SPC)-gelatin/PU. The scaffold was characterized using Fourier transform infrared (FTIR) and scanning electron microscopy (SEM) methods. Flow cytometry confirmed mesenchymal stem cells, and then the 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide (MTT) assay and DAPI staining were used to assess the in vitro biocompatibility of the scaffold. The experimental results showed that the multilayer electrospun scaffold containing 2.5% SPC could efficiently produce oxygen. Furthermore, according to cell viability results, this structure makes a suitable substrate for the coculture of keratinocytes and AMSCs. Gene expression analysis of various markers such as Involucrin, Cytokeratin 10, and Cytokeratin 14 after 14 days confirmed that keratinocytes and AMSCs coculture on PU/PCL.SPC-gelatin/PU electrospun scaffold promotes dermal differentiation and epithelial proliferation compared to keratinocytes single-cell culture. Therefore, our study supports using oxygen-releasing scaffolds as a potential strategy to hasten skin tissue regeneration. Based on the results, this structure is suggested as a promising candidate for cell-based skin tissue engineering. Given that the developed oxygen-generating polymeric electrospun scaffolds could be used as part of a future strategy for skin tissue engineering, the PU/PCL.SPC-gelatin/PU hybrid electrospun multilayer scaffold in combination with keratinocyte/AMSC coculture is proposed as an effective substrate for skin tissue engineering and regenerative medicine platforms.
尽管在过去的二十年中,组织工程学和再生医学取得了重大进展,但制造具有适当细胞的合适支架仍然被认为是该领域的一项关键成就。缺氧是慢性伤口愈合的主要障碍,这限制了组织工程计划,因为缺氧可能导致细胞死亡。本研究评估了共培养的人角质形成细胞和人脂肪间充质干细胞(AMSCs)在基于 PU/PCL 的多层释氧电纺支架上。SPC-明胶/PU。使用傅里叶变换红外(FTIR)和扫描电子显微镜(SEM)方法对支架进行了表征。流式细胞术证实了间充质干细胞,然后使用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物(MTT)测定法和 DAPI 染色来评估支架的体外生物相容性。实验结果表明,含有 2.5%SPC 的多层电纺支架能够有效地产生氧气。此外,根据细胞活力结果,这种结构为角质形成细胞和 AMSCs 的共培养提供了合适的基质。14 天后各种标志物(如 Involucrin、Cytokeratin 10 和 Cytokeratin 14)的基因表达分析证实,角质形成细胞和 AMSCs 共培养在 PU/PCL.SPC-明胶/PU 电纺支架上比角质形成细胞单细胞培养更能促进真皮分化和上皮增殖。因此,我们的研究支持使用释氧支架作为加速皮肤组织再生的潜在策略。基于这些结果,该结构被认为是细胞基皮肤组织工程的有前途的候选者。鉴于开发的含氧聚合物电纺支架可作为皮肤组织工程未来策略的一部分,因此提出了 PU/PCL.SPC-明胶/PU 杂化电纺多层支架与角质形成细胞/AMSC 共培养相结合作为皮肤组织工程和再生医学平台的有效基质。