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载药纳米粒明胶纤维缓释支架对牙周膜细胞MMPs的影响 被引量:1

Drug-loaded Nanoparticles within Gelatin Scaffolds Inhibits MMPs Expression in Periodontal Ligament Cells
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摘要 目的 :研究载免疫抑制剂SB203580的纳米粒-明胶(Ms-SB203580-gelatin)纤维缓释支架对牙周膜细胞(human periodontal ligament cells,h PDLCs)的基质金属蛋白酶(matrix metalloproteninases,MMPs)表达的影响。方法 :通过透析法制备载药纳米胶束(Micelles-SB203580,Ms-SB203580),并通过电纺法构建载纳米粒明胶支架,检测支架材料的细胞相容性和对牙周膜细胞MMP-2、MMP-13基因和蛋白的表达影响。结果:透射电镜显示载药纳米粒能负载于明胶纤维中;细胞与支架复合后增殖情况良好;实验组MMP-2、MMP-13的表达低于阳性对照组。结论:载药纳米粒明胶纤维缓释支架能明显地抑制炎症因子,可进一步应用于牙槽骨骨组织工程。 Objective: The study aimed to evaluate whether the SB203580-1oaded nanoparticles-gelatin (Ms-SB203580- gelatin) scaffolds are related to reduction of matrix metalloproteninases(MMPs) expression in human periodontal ligament cells (hPDLCs). Methods: The drug-loaded micelles (Micelles-SB203580, Ms-SB203580)was obtained by dialysis bag method and fabricate drug-loaded gelatin scaffolds by electrospining. Cell compatibility and the gene as well as protein ex- pression of MMP-2,MMP-13 were measured. Results: The gelatin scaffolds contain drug-loaded micelles were proved by TEM, The hPDLCs seeded at the scaffolds demonstrated a good biocompatibility. MMP-2 and MMP-13 expression were stain slightly in the experimental group than that of the positive group. Conclusion: The results suggest that Ms- SB203580-gelatin scaffolds have a potential to obviously reduce inflammation and may be effective for alveolar bone repair in the future.
作者 王雅冰 苏俭生 WANG Ya-bing SU Jian-sheng(Department of Prosthodontics, School and Hospital of Stomatology, Tongji University, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai 200072, Chin)
出处 《口腔颌面外科杂志》 CAS 2016年第6期385-392,共8页 Journal of Oral and Maxillofacial Surgery
基金 国家自然科学基金(81371949、81572114) 上海市科学技术委员会项目(13411951201)
关键词 免疫抑制剂 支架 牙周膜细胞 MMPS immunosuppressor scaffolds human periodontal ligament cells MMPs
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  • 1丰盛梅,高建军,金慰芳.PTH作用于老年大鼠骨髓细胞骨代谢相关基因表达的实验方法[J].复旦学报(医学版),2005,32(2):219-221. 被引量:6
  • 2高洪伟,洪天配,李琼芳.氨基胍对白细胞介素-1β所致胰岛损伤的保护作用[J].中国糖尿病杂志,1996,4(2):79-82. 被引量:3
  • 3Mancini L,Paul-Clark MJ,Rosignoli G,et al.Calcitonin and prednisolone display antagonistic actions on bone and have synergistic effects in experimental arthritis[J].Am J Paihol,2007,170(3):1018-1027.
  • 4Tanishima S,Kishimoto Y,Fukata S,et al.Minodronic acid influences receptor activator of nuclear factor κB ligand expression and suppresses bone resorption by osteoclsats in rats with collagen-induced arthritis[J].Mod Rheumatol,2007,17 (3):198-205.
  • 5Bolon B,Carter C,Daris M,et al.Adenoviral delivery of osteoprotegerin ameliorates bone resorption in a mouse ovariectomy model of osteoporosis[J].Mol Ther,2001,3(2):197-205.
  • 6Mahamed DA,Marleau A,Alnaeeli M,et al.G-anaerobes-reactive CD4+ T-cells trigger RANKL-mediated enhanced alveolar bone loss in diabetic NOD mice[J].Diabetes,2005,54(5):1477-1486.
  • 7Tak PP,Gerlag DM,Aupperle KR,et al.Inhibitor of nuclearfactor kappa B kinase beta is a key regulator of synovial inflammation[J].Arthritis Rheum,2001,44(8):1897-1907.
  • 8McIntyre KW,Shuster DJ,Gillooly KM,et al.A highly selective inhibitor of Ⅰ kappa B kinase,BMS-345541,blocks both joint inflammation and destruction in collagen-induced arthritis in mice[J].Arthritis Rheum,2003,48 (9):2652-2659.
  • 9Zhang HG,Huang N,Liu D,et al.Gene therapy that inhibits nuclear translocation of nuclear factor kappa B results in tumor necrosis factor alpha-induced apoptosis of human synovial fibroblasts[J].Arthritis Rheum,2000,43 (5):1094-1105.
  • 10Han Z,Boyle DL,Chang L,et al.c-Jun N-terminal kinase is required for metalloproteinase expression and joint destruction in inflammatory arthritis[J].J Clin Invest,2001,108(1):73-81.

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