Godoy Zanicotti Diogo, Coates Dawn Elizabeth, Duncan Warwick John
Sir John Walsh Research Institute, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.
Department of Oral Diagnostics and Surgical Sciences, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.
Clin Oral Implants Res. 2017 Jan;28(1):64-75. doi: 10.1111/clr.12761. Epub 2016 Feb 8.
The aim of this study was to investigate the capacity of adipose-derived stem cells (ADSC), grown in serum-free conditions, to regenerate bone around titanium discs with different titanium surfaces.
Ovine ADSC (oADSC) were isolated from seven sheep and cultured using serum-free and osteogenic conditions. Prior to in vivo testing, the growth and osteogenic behaviour of these cells were analysed in vitro using cell proliferation and extracellular matrix mineralisation assays. The bone regenerative capacity of autologous oADSC was evaluated in vivo on titanium discs in a sheep femur epicondyle model. Machined (MTi) and alumina-blasted (ABTi) titanium discs were used. Bone regeneration within the defects was evaluated after 1 month using histology and histomorphometry. PKH26 cell-tracking dye was used to verify the persistence of oADSC in the surgical wound.
oADSC sourced from five of seven sheep differentiated into osteoblast-like cells. Cellular proliferation was reduced only for osteogenically induced oADSC (oOS-ADSC) grown on ABTi, compared to non-induced oADSC grown on ABTi and tissue culture polystyrene (P = 0.03 and 0.02 respectively). There was no significant difference for in vitro mineralisation assays comparing oADSC with oOS-ADSC, regardless of implant surface type. oADSC labelled with PKH26 were detected 1 month after surgery within the defect. There was no difference in bone regeneration between the bone defects treated with oADSC vs. just blood clot.
After 1-month healing, the use of autologous oADSC did not improve bone regeneration in defects containing titanium devices with different surfaces.
本研究旨在探究在无血清条件下培养的脂肪来源干细胞(ADSC)在不同钛表面的钛盘周围再生骨的能力。
从7只绵羊中分离出羊ADSC(oADSC),并在无血清和成骨条件下进行培养。在体内测试之前,使用细胞增殖和细胞外基质矿化试验在体外分析这些细胞的生长和成骨行为。在绵羊股骨髁上模型的钛盘上体内评估自体oADSC的骨再生能力。使用机械加工(MTi)和氧化铝喷砂(ABTi)钛盘。1个月后使用组织学和组织形态计量学评估缺损内的骨再生情况。使用PKH26细胞追踪染料来验证oADSC在手术伤口中的持久性。
7只绵羊中有5只的oADSC分化为成骨样细胞。与在ABTi和组织培养聚苯乙烯上生长的未诱导oADSC相比,仅在ABTi上生长的成骨诱导oADSC(oOS-ADSC)的细胞增殖减少(分别为P = 0.03和0.02)。无论植入物表面类型如何,比较oADSC与oOS-ADSC的体外矿化试验均无显著差异。术后1个月在缺损内检测到用PKH26标记的oADSC。用oADSC治疗的骨缺损与仅用血凝块治疗的骨缺损之间的骨再生没有差异。
经过为期1个月的愈合后,使用自体oADSC并未改善在含有不同表面的钛装置的缺损中的骨再生。