Hwang Nathaniel S, Varghese Shyni, Lee H Janice, Zhang Zijun, Ye Zhaohui, Bae Jongwoo, Cheng Linzhao, Elisseeff Jennifer
Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Proc Natl Acad Sci U S A. 2008 Dec 30;105(52):20641-6. doi: 10.1073/pnas.0809680106. Epub 2008 Dec 18.
Development of clinically relevant regenerative medicine therapies using human embryonic stem cells (hESCs) requires production of a simple and readily expandable cell population that can be directed to form functional 3D tissue in an in vivo environment. We describe an efficient derivation method and characterization of mesenchymal stem cells (MSCs) from hESCs (hESCd-MSCs) that have multilineage differentiation potential and are capable of producing fat, cartilage, and bone in vitro. Furthermore, we highlight their in vivo survival and commitment to the chondrogenic lineage in a microenvironment comprising chondrocyte-secreted morphogenetic factors and hydrogels. Normal cartilage architecture was established in rat osteochondral defects after treatment with chondrogenically-committed hESCd-MSCs. In view of the limited available cell sources for tissue engineering applications, these embryonic-derived cells show significant potential in musculoskeletal tissue regeneration applications.
利用人类胚胎干细胞(hESCs)开发具有临床相关性的再生医学疗法,需要产生一种简单且易于扩增的细胞群体,该细胞群体能够在体内环境中定向形成功能性三维组织。我们描述了一种从hESCs高效衍生间充质干细胞(MSCs,即hESCd-MSCs)的方法及其特性,这些细胞具有多谱系分化潜能,能够在体外产生脂肪、软骨和骨。此外,我们强调了它们在包含软骨细胞分泌的形态发生因子和水凝胶的微环境中的体内存活能力以及向软骨谱系的定向分化能力。在用向软骨定向分化的hESCd-MSCs治疗后,大鼠骨软骨缺损处建立了正常的软骨结构。鉴于组织工程应用中可用细胞来源有限,这些胚胎来源的细胞在肌肉骨骼组织再生应用中显示出巨大潜力。