Wen Li, Wang Yu, Wen Ning, Yuan Gongjie, Wen Mingling, Zhang Liang, Liu Qian, Liang Yuan, Cai Chuan, Chen Xin, Ding Yin
1 Department of Orthodontics, School of Stomatology, Fourth Military Medical University , Xi'an, China .
2 Institute of Stomatology, Chinese PLA General Hospital , Beijing, China .
Stem Cells Dev. 2016 Jan 15;25(2):123-38. doi: 10.1089/scd.2015.0049. Epub 2015 Dec 18.
A hot issue in current research regarding stem cells for regenerative medicine is the retainment of the stemness and multipotency of stem cell. Endothelial progenitor cells (EPCs) are characterized by an angiogenic switch that induces angiogenesis and further ameliorates the local microenvironment in ischemic organs. This study investigated whether EPCs could modulate the multipotent and differential abilities of mesenchymal stem cells (MSCs) in vitro and in vivo. We established an EPC/MSC indirect Transwell coculture system and then examined the effects of EPCs on the regulation of MSC biological properties in vitro and bone formation in vivo. The in vitro studies showed that cocultured MSCs (coMSCs) display no overt changes in cell morphology but an enhanced MSC phenotype compared with monocultured MSCs (monoMSCs). Our studies regarding the cellular, molecular, and protein characteristics of coMSCs and monoMSCs demonstrated that EPCs greatly promote the proliferation and differentiation potentials of coMSCs under indirect coculture condition. The expression of the pluripotency factors OCT4, SOX2, Nanog, and Klf4 was also upregulated in coMSCs. Furthermore, coMSCs combined with fibrin glue showed improved bone regeneration when used to repair rat alveolar bone defects compared with monoMSC grafts in vivo. This study is the first to demonstrate that EPCs have dynamic roles in maintaining MSC stemness and regulating MSC differentiation potential.
当前关于用于再生医学的干细胞研究中的一个热点问题是干细胞干性和多能性的维持。内皮祖细胞(EPCs)的特征在于一种血管生成转换,可诱导血管生成并进一步改善缺血器官中的局部微环境。本研究调查了EPCs在体外和体内是否能够调节间充质干细胞(MSCs)的多能性和分化能力。我们建立了EPC/MSC间接Transwell共培养系统,然后检测EPCs对体外MSC生物学特性调节以及体内骨形成的影响。体外研究表明,与单培养的MSCs(monoMSCs)相比,共培养的MSCs(coMSCs)细胞形态无明显变化,但MSC表型增强。我们对coMSCs和monoMSCs的细胞、分子和蛋白质特征的研究表明,在间接共培养条件下,EPCs极大地促进了coMSCs的增殖和分化潜能。共培养的MSCs中多能性因子OCT4、SOX2、Nanog和Klf4的表达也上调。此外,与体内的单培养MSC移植物相比,共培养的MSCs与纤维蛋白胶联合用于修复大鼠牙槽骨缺损时,显示出更好的骨再生效果。本研究首次证明EPCs在维持MSC干性和调节MSC分化潜能方面具有动态作用。