Nilforoushzadeh Mohammad Ali, Khodadadi Yazdi Mohsen, Baradaran Ghavami Shaghayegh, Farokhimanesh Samila, Mohammadi Amirabad Leila, Zarrintaj Payam, Saeb Mohammad Reza, Hamblin Michael R, Zare Mehrak, Mozafari Masoud
Skin and Stem Cell Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
ACS Biomater Sci Eng. 2020 Sep 14;6(9):5096-5109. doi: 10.1021/acsbiomaterials.0c00988. Epub 2020 Aug 27.
The ability of mesenchymal stem cells (MSCs) to enhance cutaneous wound healing has been well established. Extensive expansion of cells to reach sufficient cell numbers for regenerating tissues has always limited cell-based therapies. An ingenious solution to address this challenge is to develop a strategy to increase the immunomodulatory effects of MSCs without expanding them. In this study, we employed a simple characteristic of cells. It was observed that an optimized three-dimensional (3D) MSC culture in spheroid forms significantly improved their paracrine effects. An electrospray (ES) encapsulation apparatus was used to encapsulate individual or 3D spheroid MSCs into microscale alginate beads (microbeads). Furthermore, alginate microbeads were embedded in an injectable thermosensitive hydrogel matrix, which gels at skin temperature. The hydrogel fills and seals the wounds cavities, maintains high humidity at the wound area, absorbs exudate, and fixes microbeads, protecting them from direct contact with the harsh wound environment. In vitro investigations revealed that secretion of interleukin 10 (IL-0) and transforming growth factor β1 (TGF-β1) gene was gradually enhanced, providing a delivery platform for prolonged release of bioactive molecules. In vivo study on full-thickness wounds showed granulation and re-epithelialization, only after 7 days. Moreover, increased expression of α-smooth muscle actin (α-SMA) in the first 14 days after treatment ensured wound contraction. Besides, a gradual decrease in α-SMA secretion resulted in reduced scar formation. Well-organized collagen fibrils and high expression of the angiogenesis biomarker CD31 confirmed the promoting effect of the hydrogel on the wound-healing process. The proposed wound-dressing system would potentially be used in scalable and effective cell-based wound therapies.
间充质干细胞(MSCs)促进皮肤伤口愈合的能力已得到充分证实。为获得足够数量的细胞以用于组织再生而进行的大量细胞扩增一直限制着基于细胞的疗法。解决这一挑战的一个巧妙方法是制定一种策略,在不扩增MSCs的情况下增强其免疫调节作用。在本研究中,我们利用了细胞的一个简单特性。据观察,呈球体形式的优化三维(3D)MSCs培养显著改善了它们的旁分泌作用。使用电喷雾(ES)封装设备将单个或3D球体MSCs封装入微尺度藻酸盐珠(微珠)中。此外,将藻酸盐微珠嵌入可注射的热敏水凝胶基质中,该基质在皮肤温度下凝胶化。水凝胶填充并封闭伤口腔,在伤口区域保持高湿度,吸收渗出液,并固定微珠,保护它们不与恶劣的伤口环境直接接触。体外研究表明,白细胞介素10(IL - 0)和转化生长因子β1(TGF - β1)基因的分泌逐渐增强,为生物活性分子的长效释放提供了一个递送平台。对全层伤口的体内研究显示,仅在7天后就出现了肉芽组织形成和再上皮化。此外,治疗后前14天α平滑肌肌动蛋白(α - SMA)表达增加确保了伤口收缩。此外,α - SMA分泌的逐渐减少导致瘢痕形成减少。排列良好的胶原纤维和血管生成生物标志物CD31的高表达证实了水凝胶对伤口愈合过程的促进作用。所提出的伤口敷料系统可能会用于可扩展且有效的基于细胞的伤口治疗。