...
首页> 外文期刊>Frontiers in Physiology >NZ-GMP Approved Serum Improve hDPSC Osteogenic Commitment and Increase Angiogenic Factor Expression
【24h】

NZ-GMP Approved Serum Improve hDPSC Osteogenic Commitment and Increase Angiogenic Factor Expression

机译:NZ-GMP批准的血清可改善hDPSC成骨作用并增加血管生成因子的表达

获取原文
           

摘要

Human dental pulp stem cells (hDPSCs), selected from the stromal-vascular fraction of dental pulp, are ecto-mesenchymal stem cells deriving from neural crests, successfully used in human bone tissue engineering. For their use in human therapy GMP procedures are required. For instance, the use of fetal bovine serum (FBS) is strongly discouraged in clinical practice due to its high risk of prions and other infections for human health. Alternatively, clinical grade sera have been suggested, including the New Zealand FBS (NZ-FBS). Therefore, the aim of this study was to evaluate the behavior of hDPSCs expanded in culture medium containing NZ-FBS. Since it was widely demonstrated hDPSCs display relevant capabilities to differentiate into osteogenic and angiogenic lineages, we performed a comparative study to assess if these features are also retained by cultivating the cells with a safer serum never tested on this cell line. hDPSCs were grown using NZ-FBS and conventional (C-FBS) for 7, 14, and 21 days, in both 2D and 3D cultures. Growth curves, expression of bone-related markers, calcification and angiogenesis were evaluated. NZ-FBS induced significant cell growth with respect to C-FBS and promoted an earlier increase expression of osteogenic markers, in particular of those involved in the formation of mineralized matrix (BSP and OPN) within 14 days. In addition, hDPSCs cultured in presence of NZ-FBS were found to produce higher mRNA levels of the angiogenic factors, such as VEGF and PDGFA. Taken together, our results highlight that hDPSCs proliferate, enhance their osteogenic commitment and increase angiogenic factors in NZ-FBS containing medium. These features have also been found when hDPSC were seeded on the clinical-grade collagen I scaffold (Bio-Gide?), leading to the conclusion that for human therapy some procedures and above all the use of GMP-approved materials have no negative impact.
机译:选自牙髓基质-血管部分的人类牙髓干细胞(hDPSC)是源自神经c的外间充质干细胞,已成功用于人体骨组织工程中。为了将其用于人体治疗,需要执行GMP程序。例如,在临床实践中强烈建议不要使用胎牛血清(FBS),因为它对人类健康具有很高的human病毒和其他感染风险。或者,已建议使用临床级血清,包括新西兰FBS(NZ-FBS)。因此,本研究的目的是评估在含有NZ-FBS的培养基中扩增的hDPSC的行为。由于已广泛证明hDPSCs具有分化成骨和血管生成谱系的相关能力,因此我们进行了一项比较研究,以通过使用从未在该细胞系上测试过的更安全的血清培养细胞来评估这些特征是否也得以保留。在2D和3D培养中,使用NZ-FBS和常规(C-FBS)将hDPSCs培养7、14和21天。评价生长曲线,骨相关标志物的表达,钙化和血管生成。相对于C-FBS,NZ-FBS诱导了显着的细胞生长,并促进了成骨标记物,特别是14天之内参与矿化基质形成的成骨标记物(BSP和OPN)的表达增加。另外,发现在NZ-FBS存在下培养的hDPSCs产生较高水平的血管生成因子,例如VEGF和PDGFA的mRNA水平。两者合计,我们的结果表明,hDPSCs在含有NZ-FBS的培养基中增殖,增强其成骨作用并增加血管生成因子。当将hDPSC接种在临床级胶原I支架(Bio-Gide?)上时,也发现了这些特征,从而得出结论,对于人类治疗,某些程序尤其是使用GMP认可的材料不会产生负面影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号