Li Limei, Yu Mali, Li Yao, Li Qing, Yang Hongcai, Zheng Meng, Han Yi, Lu Di, Lu Sheng, Gui Li
Yunnan Key Laboratory of Stem Cell and Regenerative Medicine, Science and Technology Achievement Incubation Center, Kunming Medical University, Kunming, 650500, China.
Department of Stomatology, The First People's Hospital of Yunnan Province, Kunming, 650032, China.
Bioact Mater. 2020 Nov 8;6(5):1255-1266. doi: 10.1016/j.bioactmat.2020.10.018. eCollection 2021 May.
The development of functional materials for osteoporosis is ultimately required for bone remodeling. However, grafts were accompanied by increasing pro-inflammatory cytokines that impaired bone formation. In this work, nano-hydroxyapatite (n-HA)/resveratrol (Res)/chitosan (CS) composite microspheres were designed to create a beneficial microenvironment and help improve the osteogenesis by local sustained release of Res. Study of release confirmed the feasibility of n-HA/Res/CS microspheres for controlled Res release. Notably, microspheres had anti-inflammatory activity evidenced by the decreased expression of pro-inflammatory cytokines TNF-α, IL-1β and iNOS in RAW264.7 cells in a dose dependent manner. Further, enhanced adhesion and proliferation of BMSCs seeded onto microspheres demonstrated that composite microspheres were conducive to cell growth. The ability to enhance osteo-differentiation was supported by up-regulation of Runx2, ALP, Col-1 and OCN, and substantial mineralization in osteogenic medium. When implanted into bone defects in the osteoporotic rat femoral condyles, enhanced entochondrostosis and bone regeneration suggested that the n-HA/Res/CS composite microspheres were more favorable for impaired fracture healing. The results indicated that optimized n-HA/Res/CS composite microspheres could serve as promising multifunctional fillers for osteoporotic bone defect/fracture treatment.
骨质疏松症功能材料的开发最终是骨重塑所必需的。然而,移植物伴随着促炎细胞因子的增加,这会损害骨形成。在这项工作中,设计了纳米羟基磷灰石(n-HA)/白藜芦醇(Res)/壳聚糖(CS)复合微球,以创造有益的微环境,并通过Res的局部持续释放来帮助改善骨生成。释放研究证实了n-HA/Res/CS微球用于Res控释的可行性。值得注意的是,微球具有抗炎活性,这在RAW264.7细胞中促炎细胞因子TNF-α、IL-1β和iNOS的表达以剂量依赖性方式降低中得到证明。此外,接种到微球上的骨髓间充质干细胞(BMSCs)的粘附和增殖增强,表明复合微球有利于细胞生长。Runx2、碱性磷酸酶(ALP)、I型胶原(Col-1)和骨钙素(OCN)的上调以及在成骨培养基中的大量矿化支持了增强骨分化的能力。当植入骨质疏松大鼠股骨髁的骨缺损中时,增强的软骨内成骨和骨再生表明n-HA/Res/CS复合微球对受损骨折愈合更有利。结果表明,优化后的n-HA/Res/CS复合微球可作为治疗骨质疏松性骨缺损/骨折的有前景的多功能填充剂。