Fabrication of gelatin methacrylate/nanohydroxyapatite microgel arrays for periodontal tissue regeneration

牙周膜干细胞 明胶 材料科学 再生(生物学) 体内 组织工程 生物医学工程 运行x2 纳米技术 化学 细胞生物学 碱性磷酸酶 体外 成骨细胞 医学 生物 生物化学 生物技术
作者
Xi Chen,Shizhu Bai,Bei Li,Huan Liu,Guofeng Wu,Sha Li,Yimin Zhao
出处
期刊:International Journal of Nanomedicine [Dove Medical Press]
卷期号:Volume 11: 4707-4718 被引量:50
标识
DOI:10.2147/ijn.s111701
摘要

Introduction:Periodontitis is a chronic infectious disease and is the major cause of tooth loss and other oral health issues around the world.Periodontal tissue regeneration has therefore always been the ultimate goal of dentists and researchers.Existing fabrication methods mainly focused on a top-down tissue engineering strategy in which several drawbacks remain, including low throughput and limited diffusion properties resulting from a large sample size.Gelatin methacrylate (GelMA) is a kind of photocrosslinkable and biocompatible hydrogel, with the capacities of enabling cell encapsulation and regeneration of functional tissues.Here, we developed a novel method to fabricate GelMA/nanohydroxylapatite (nHA) microgel arrays using a photocrosslinkable strategy.The viability, proliferation, and osteogenic differentiation and in vivo osteogenesis of human periodontal ligament stem cells (hPDLSCs) encapsulated in microgels were evaluated.The results suggested that such microgels provide great potential for periodontal tissue repair and regeneration.Methods: Microgel arrays were fabricated by blending different weight ratios of GelMA and nHA.hPDLSCs were encapsulated in GelMA/nHA microgels of various ratios for a systematic evaluation of cell viability, proliferation, and osteogenic differentiation.In vivo osteogenesis in nude mice was also studied. Results:The GelMA/nHA microgels exhibited appropriate microarchitecture, mechanical strength, and surface roughness, thus enabling cell adhesion and proliferation.Additionally, the GelMA/nHA microgels (10%/2% w/v) enhanced the osteogenic differentiation of hPDLSCs by elevating the expression levels of osteogenic biomarker genes, such as ALP, BSP, OCN, and RUNX2.In vivo ectopic transplantation results showed that GelMA/nHA microgels (10%/2% w/v) increased mineralized tissue formation with abundant vascularization, compared with the 1%, 3%, and the pure GelMA group. Conclusion:The GelMA/nHA microgels (10%/2% w/v) facilitated hPDLSCs viability, proliferation, and osteogenic differentiation in vitro and further promoted new bone formation in vivo, suggesting that the GelMA/nHA microgels (10%/2% w/v) provide great potential for periodontal tissue regeneration.

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