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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >In vivo osteogenic capability of cultured allogeneic bone in porous hydroxyapatite: immunosuppressive and osteogenic potential of FK506 in vivo.
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In vivo osteogenic capability of cultured allogeneic bone in porous hydroxyapatite: immunosuppressive and osteogenic potential of FK506 in vivo.

机译:在多孔羟基磷灰石中培养的同种异体骨的体内成骨能力:FK506的体内免疫抑制和成骨潜力。

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摘要

Fischer or ACI rat marrow cells were obtained from femoral shafts and were cultured to confluence in Eagle's minimal essential medium (EMEM) supplemented with 15% fetal bovine serum. After trypsinization, the cells were subcultured on porous hydroxyapatite (HA; Interpore 500) blocks in the presence of beta-glycerophosphate and 10 nM dexamethasone (Dex). After 2 weeks of subculture, a mineralized bone matrix with osteogenic cells developed on the HA pore surfaces. ACI or Fischer cultured bone tissue/HA constructs were implanted subcutaneously into the backs of Fischer rats and the immunosuppressant FK506 was given to the rats for 4 weeks. Implants were harvested 4 weeks and 8 weeks after insertion. At 4 weeks, the ACI constructs (allografts) showed high levels of osteogenic parameters (alkaline phosphatase [ALP] activity and osteocalcin content) and bone formation was observed together with active osteoblasts without obvious accumulation of inflammatory cells. At 8 weeks, active osteoblasts and progressive bone formation were still observed, while osteogenic parameters remained high and osteocalcin messenger RNA (mRNA) was detected. Without FK506 administration, the allografts showed neither bone formation nor osteocalcin mRNA and there were only trace levels of the osteogenic parameters. In the case of Fischer constructs (isografts), extensive bone formation was detected and all the osteogenic parameters were higher with FK506 than without FK506 at both 4 weeks and 8 weeks. These results indicate that cultured bone tissue/HA constructs possess a high osteogenic potential, even as allografts, and that FK506 not only has an immunosuppressive action, but also promotes bone formation.
机译:从股骨干获得Fischer或ACI大鼠骨髓细胞,并在补充有15%胎牛血清的Eagle基本必需培养基(EMEM)中培养至汇合。胰蛋白酶消化后,在存在β-甘油磷酸酯和10 nM地塞米松(Dex)的情况下,将细胞在多孔羟基磷灰石(HA; Interpore 500)块上继代培养。继代培养2周后,HA孔表面形成了具有成骨细胞的矿化骨基质。将ACI或Fischer培养的骨组织/ HA构建体皮下植入Fischer大鼠的背部,并将免疫抑制剂FK506给予大鼠4周。植入后4周和8周收获植入物。在第4周时,ACI构造(同种异体移植物)显示出高水平的成骨参数(碱性磷酸酶[ALP]活性和骨钙素含量),观察到骨形成以及活跃的成骨细胞,而没有明显的炎症细胞聚集。在第8周,仍观察到活跃的成骨细胞和进行性骨形成,而成骨参数仍然很高,并且检测到骨钙蛋白信使RNA(mRNA)。如果不使用FK506,同种异体移植物既没有显示出骨形成也没有显示出骨钙素mRNA,并且只有微量的成骨参数。对于Fischer构建体(同种异体移植物),在第4周和第8周,检测到广泛的骨形成,并且FK506的所有成骨参数均高于FK506。这些结果表明,即使同种异体移植,培养的骨组织/ HA构建体也具有很高的成骨潜力,并且FK506不仅具有免疫抑制作用,而且还可以促进骨形成。

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