Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892, USA.
Tissue Eng Part B Rev. 2011 Dec;17(6):423-30. doi: 10.1089/ten.teb.2011.0199. Epub 2011 Jul 28.
Based on the extensive investigation of various ways to regenerate bone, bone marrow stromal cells, in conjunction with ceramic scaffolds, show great promise for application in human patients, and are already in use in a limited number of clinical trials. In preparing for clinical trials, scale-up current good manufacturing processes (cGMP) must incorporate the use of appropriate assays to ensure that the resulting cell product has maintained its biological activity. Future developments are needed to identify better scaffolds, and better ways to deliver cells with either injectable carriers, or by developing techniques to aide in their escape from the circulation and their incorporation into the pre-existing tissue. Lastly, development of methods that faithfully direct pluripotent stem cell differentiation into populations of osteogenic precursors (and ideally, containing skeletal stem cells) represents a new challenge in the field of bone regeneration, but also offer new opportunities to not only to study the biology of bone formation, but also to develop a robust cell source for bone regeneration.
基于对各种骨再生方法的广泛研究,骨髓基质细胞与陶瓷支架结合,显示出在人类患者中应用的巨大潜力,并且已经在有限数量的临床试验中使用。在为临床试验做准备时,扩大现行良好生产规范(cGMP)必须结合使用适当的检测方法,以确保最终的细胞产品保持其生物活性。未来的发展需要确定更好的支架,以及更好的方法来输送细胞,无论是使用可注射载体,还是开发技术来帮助它们逃离循环并将其整合到现有的组织中。最后,开发能够忠实指导多能干细胞分化为成骨前体细胞(理想情况下,包含骨干/基质细胞)的方法,代表了骨再生领域的一个新挑战,但也为不仅研究骨形成的生物学,而且开发用于骨再生的强大细胞来源提供了新的机会。