Coyle Ali, Chakraborty Aishik, Huang Jiaqi, Shamiya Yasmeen, Luo Wei, Paul Arghya
School of Biomedical Engineering, The University of Western Ontario, London, ON, N6A 5B9, Canada.
Department of Chemical and Biochemical Engineering, The University of Western Ontario, London, ON, N6A 5B9, Canada.
Adv Healthc Mater. 2025 Feb;14(4):e2402701. doi: 10.1002/adhm.202402701. Epub 2025 Jan 5.
Prevalence of osteoarthritis has been increasing in aging populations, which has necessitated the use of advanced biomedical treatments. These involve grafts or delivering drug molecules entrapped in scaffolds. However, such treatments often show suboptimal therapeutic effects due to poor half-life and off-target effects of drug molecules. As a countermeasure, a 3D printable robust hydrogel-based tissue-repair platform is developed containing decellularized extracellular matrix (dECM) from differentiated mammalian cells as the therapeutic cargo. Here, pre-osteoblastic and pre-chondrogenic murine cells are differentiated in vitro, decellularized, and incorporated into methacrylated gelatin (GelMA) solutions to form osteogenic (GelO) and chondrogenic (GelC) hydrogels, respectively. Integrating the bioactive dECM from differentiated cell sources allows GelO and GelC to induce differentiation in human adipose-derived stem cells (hASCs) toward osteogenic and chondrogenic lineages. Further, GelO and GelC can be covalently adhered using a carbodiimide coupling reaction, forming a multi-layered hydrogel with potential application as a bioactive osteochondral plug. The designed multi-layered hydrogel can also induce differentiation of hASCs in vitro. In conclusion, the bioactive dECM carrying 3D printed robust hydrogel offers a promising new drug and cell-free therapeutic strategy for bone and cartilage repair and future osteoarthritis management.
骨关节炎在老年人群中的患病率一直在上升,这使得先进的生物医学治疗方法的使用成为必要。这些治疗方法包括移植或递送包裹在支架中的药物分子。然而,由于药物分子的半衰期短和脱靶效应,此类治疗往往显示出次优的治疗效果。作为一种对策,开发了一种基于3D可打印的坚固水凝胶的组织修复平台,该平台包含来自分化的哺乳动物细胞的脱细胞细胞外基质(dECM)作为治疗载体。在这里,前成骨细胞和前软骨生成小鼠细胞在体外分化、脱细胞,并分别掺入甲基丙烯酸化明胶(GelMA)溶液中,以形成成骨(GelO)水凝胶和软骨生成(GelC)水凝胶。整合来自分化细胞来源的生物活性dECM可使GelO和GelC诱导人脂肪来源干细胞(hASC)向成骨和成软骨谱系分化。此外,GelO和GelC可以使用碳二亚胺偶联反应共价粘附,形成一种多层水凝胶,具有作为生物活性骨软骨塞的潜在应用。所设计的多层水凝胶还可以在体外诱导hASC的分化。总之,携带3D打印坚固水凝胶的生物活性dECM为骨和软骨修复以及未来骨关节炎管理提供了一种有前景的新型无药物和无细胞治疗策略。