Ozhava Derya, Bektas Cemile, Lee Kathleen, Jackson Anisha, Mao Yong
Laboratory for Biomaterials Research, Department of Chemistry and Chemical Biology, Rutgers University, 145 Bevier Rd., Piscataway, NJ 08854, USA.
Department of Chemistry and Chemical Processing Technologies, Cumra Vocational School, Selcuk University, 42130 Konya, Turkey.
Gels. 2024 Jan 26;10(2):97. doi: 10.3390/gels10020097.
The demand for innovative therapeutic interventions to expedite wound healing, particularly in vulnerable populations such as aging and diabetic patients, has prompted the exploration of novel strategies. Mesenchymal stem cell (MSC)-based therapy emerges as a promising avenue for treating acute and chronic wounds. However, its clinical application faces persistent challenges, notably the low survivability and limited retention time of engraftment in wound environments. Addressing this, a strategy to sustain the viability and functionality of human MSCs (hMSCs) in a graft-able format has been identified as crucial for advanced wound care. Hydrogel microparticles (HMPs) emerge as promising entities in the field of wound healing, showcasing versatile capabilities in delivering both cells and bioactive molecules/drugs. In this study, gelatin HMPs (GelMPs) were synthesized via an optimized mild processing method. GelMPs with distinct diameter sizes were sorted and characterized. The growth of hMSCs on GelMPs with various sizes was evaluated. The release of wound healing promoting factors from hMSCs cultured on different GelMPs were assessed using scratch wound assays and gene expression analysis. GelMPs with a size smaller than 100 microns supported better cell growth and cell migration compared to larger sizes (100 microns or 200 microns). While encapsulation of hMSCs in hydrogels has been a common route for delivering viable hMSCs, we hypothesized that hMSCs cultured on GelMPs are more robust than those encapsulated in hydrogels. To test this hypothesis, hMSCs were cultured on GelMPs or in the cross-linked methacrylated gelatin hydrogel (GelMA). Comparative analysis of growth and wound healing effects revealed that hMSCs cultured on GelMPs exhibited higher viability and released more wound healing activities in vitro. This observation highlights the potential of GelMPs, especially those with a size smaller than 100 microns, as a promising carrier for delivering hMSCs in wound healing applications, providing valuable insights for the optimization of advanced therapeutic strategies.
对创新治疗干预措施的需求日益增长,旨在加速伤口愈合,尤其是在老年和糖尿病患者等弱势群体中,这促使人们探索新的策略。基于间充质干细胞(MSC)的疗法成为治疗急性和慢性伤口的一条有前景的途径。然而,其临床应用面临持续挑战,尤其是在伤口环境中的低存活率和有限的植入保留时间。为解决这一问题,一种以可移植形式维持人MSC(hMSC)活力和功能的策略已被确定为高级伤口护理的关键。水凝胶微粒(HMP)在伤口愈合领域成为有前景的实体,在递送细胞和生物活性分子/药物方面展现出多种能力。在本研究中,通过优化的温和加工方法合成了明胶水凝胶微粒(GelMP)。对具有不同直径大小的GelMP进行了分类和表征。评估了hMSC在不同大小的GelMP上的生长情况。使用划痕试验和基因表达分析评估了在不同GelMP上培养的hMSC释放促进伤口愈合因子的情况。与较大尺寸(100微米或200微米)相比,尺寸小于100微米的GelMP支持更好的细胞生长和细胞迁移。虽然将hMSC封装在水凝胶中一直是递送活hMSC的常见途径,但我们假设在GelMP上培养的hMSC比封装在水凝胶中的hMSC更具活力。为验证这一假设,将hMSC培养在GelMP上或交联的甲基丙烯酸化明胶水凝胶(GelMA)中。生长和伤口愈合效果的比较分析表明,在GelMP上培养的hMSC在体外表现出更高的活力并释放更多的伤口愈合活性。这一观察结果突出了GelMP的潜力,尤其是那些尺寸小于100微米的GelMP,作为在伤口愈合应用中递送hMSC的有前景的载体,为优化高级治疗策略提供了有价值的见解。