Lin Tzu-Hsiang, Wang Hsueh-Chun, Tseng Yau-Lin, Yeh Ming-Long
Department of Biomedical Engineering, College of Engineering, National Cheng Kung University, 1 University Rd., Tainan, 701, Taiwan.
Department of Surgery, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, 1 University Rd., Tainan, 701, Taiwan.
Mater Today Bio. 2024 Aug 3;28:101174. doi: 10.1016/j.mtbio.2024.101174. eCollection 2024 Oct.
Articular cartilage regeneration is a major challenge in orthopedic medicine. Endothelial progenitor cells (EPCs) are a promising cell source for regenerative medicine applications. However, their roles and functions in cartilage regeneration are not well understood. Additionally, thermosensitive chitosan hydrogels have been widely used in tissue engineering, but further development of these hydrogels incorporating vascular lineage cells for cartilage repair is insufficient. Thus, this study aimed to characterize the ability of EPCs to undergo endothelial-mesenchymal stem cell transdifferentiation and chondrogenic differentiation and investigate the ability of chondrogenic EPC-seeded thermosensitive chitosan-graft-poly (-isopropylacrylamide) (CEPC-CSPN) scaffolds to improve healing in a rabbit osteochondral defect (OCD) model. EPCs were isolated and endothelial-to-mesenchymal transition (EndMT) was induced by transforming growth factor-β1 (TGF-β1); these EPCs are subsequently termed transdifferentiated EPCs (tEPCs). The stem cell-like properties and chondrogenic potential of tEPCs were evaluated by a series of assays. Furthermore, the effect of CEPC-CSPN scaffolds on OCD repair was evaluated. Our results confirmed that treatment of EPC with TGF-β1 induced EndMT and the acquisition of stem cell-like properties, producing tEPCs. Upon inducing chondrogenic differentiation of tEPCs (CEPCs), the cells exhibited significantly enhanced chondrogenesis and chondrocyte surface markers after 25 days. The TGF-β1-induced differentiation of EPCs is mediated by both the TGF-β/Smad and extracellular signal-regulated kinase (Erk) pathways. The CEPC-CSPN scaffold reconstructed well-integrated translucent cartilage and repaired subchondral bone , exhibiting regenerative capacity. Collectively, our results suggest that the CEPC-CSPN scaffold induces OCD repair, representing a promising approach to articular cartilage regeneration.
关节软骨再生是骨医学中的一项重大挑战。内皮祖细胞(EPCs)是再生医学应用中一种很有前景的细胞来源。然而,它们在软骨再生中的作用和功能尚未得到充分了解。此外,热敏壳聚糖水凝胶已广泛应用于组织工程,但将这些水凝胶与血管谱系细胞结合用于软骨修复的进一步开发还不够。因此,本研究旨在表征EPCs进行内皮-间充质干细胞转分化和软骨分化的能力,并研究接种软骨生成EPC的热敏壳聚糖接枝聚(异丙基丙烯酰胺)(CEPC-CSPN)支架改善兔骨软骨缺损(OCD)模型愈合的能力。分离EPCs,并通过转化生长因子-β1(TGF-β1)诱导内皮-间充质转化(EndMT);这些EPCs随后被称为转分化EPCs(tEPCs)。通过一系列试验评估tEPCs的干细胞样特性和软骨生成潜力。此外,评估了CEPC-CSPN支架对OCD修复的影响。我们的结果证实,用TGF-β1处理EPCs可诱导EndMT并获得干细胞样特性,产生tEPCs。在诱导tEPCs(CEPCs)软骨分化后,细胞在25天后表现出显著增强的软骨生成和软骨细胞表面标志物。TGF-β1诱导的EPCs分化由TGF-β/Smad和细胞外信号调节激酶(Erk)途径介导。CEPC-CSPN支架重建了整合良好的半透明软骨并修复了软骨下骨,表现出再生能力。总体而言,我们的结果表明,CEPC-CSPN支架可诱导OCD修复,是关节软骨再生的一种有前景的方法。