Department of Bioengineering; University of Pittsburgh, Pittsburgh, PA 15213, United States of America. Center for Craniofacial Regeneration; University of Pittsburgh, Pittsburgh, PA 15213, United States of America.
Biomed Mater. 2020 May 18;15(4):045006. doi: 10.1088/1748-605X/ab401f.
The ideal combination of hydrogel components for regeneration of cartilage and cartilaginous interfaces is a significant challenge because control over differentiation into multiple lineages is necessary. Stabilization of the phenotype of stem cell derived chondrocytes is needed to avoid undesired progression to terminal hypertrophy and tissue mineralization. A novel ternary blend hydrogel composed of methacrylated poly(ethylene glycol) (PEG), gelatin, and heparin (PGH) was designed to guide chondrogenesis by bone marrow derived mesenchymal stem cells (BMSCs) and maintenance of their cartilaginous phenotype. The hydrogel material effects on chondrogenic and osteogenic differentiation by BMSCs were evaluated in comparison to methacrylated gelatin hydrogel (GEL), a conventional bioink used for both chondrogenic and osteogenic applications. PGH and GEL hydrogels were loaded with goat BMSCs and cultured in chondrogenic and osteogenic mediums in vitro over six weeks. The PGH showed no sign of mineral deposition in an osteogenic environment in vitro. To further evaluate material effects, the hydrogels were loaded with adult human BMSCs (hBMSCs) and transforming growth factor β-3 and grown in subcutaneous pockets in mice over eight weeks. Consistent with the in vitro results, the PGH had greater potential to induce chondrogenesis by BMSCs in vivo compared to the GEL as evidenced by elevated gene expression of chondrogenic markers, supporting its potential for stable cartilage engineering. The PGH also showed a greater percentage of GAG positive cells compared to the GEL. Unlike the GEL, the PGH hydrogel exhibited anti-osteogenic effects in vivo as evidenced by negative Von Kossa staining and suppressed gene expression of hypertrophic and osteogenic markers. By nature of their polymer composition alone, the PGH and GEL regulated BMSC differentiation down different osteochondral lineages. Thus, the PGH and GEL are promising hydrogels to regenerate stratified cartilaginous interfacial tissues in situ, such as the mandibular condyle surface, using undifferentiated BMSCs and a stratified scaffold design.
用于软骨和软骨界面再生的水凝胶成分的理想组合是一个重大挑战,因为需要控制其向多个谱系分化。需要稳定干细胞来源的软骨细胞的表型,以避免向终末肥大和组织矿化的不可控进展。设计了一种由甲基丙烯酰化聚乙二醇(PEG)、明胶和肝素(PGH)组成的新型三元共混水凝胶,通过骨髓间充质干细胞(BMSCs)引导软骨生成,并维持其软骨表型。与用于软骨生成和成骨应用的传统生物墨水甲基丙烯酰化明胶水凝胶(GEL)相比,评估了水凝胶材料对 BMSCs 软骨生成和成骨分化的影响。将 PGH 和 GEL 水凝胶与山羊 BMSCs 负载并在体外分别于软骨和成骨培养基中培养六周。在体外成骨环境中,PGH 没有出现矿化沉积的迹象。为了进一步评估材料的影响,将水凝胶负载成人源 BMSCs(hBMSCs)和转化生长因子β-3,并在小鼠皮下囊中培养八周。与体外结果一致,PGH 比 GEL 更有潜力在体内通过 BMSCs 诱导软骨生成,证据是软骨生成标志物的基因表达升高,支持其稳定软骨工程的潜力。PGH 与 GEL 相比,也显示出更多的 GAG 阳性细胞百分比。与 GEL 不同,PGH 水凝胶在体内表现出抗成骨作用,证据是阴性的 Von Kossa 染色和抑制肥大和成骨标志物的基因表达。仅通过其聚合物组成,PGH 和 GEL 就可以调节 BMSC 沿着不同的骨软骨谱系分化。因此,PGH 和 GEL 是有前途的水凝胶,可以使用未分化的 BMSCs 和分层支架设计,原位再生分层软骨界面组织,如下颌骨髁突表面。