Ye Lanfeng, Chen Lin, Feng Fan, Cui Junhui, Li Kaide, Li Zhiyong, Liu Lei
State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, 610041, P. R. China.
Department of Oral and Maxillofacial Surgery, The Second Xiangya Hospital, Central South University, Changsha, 410011, P. R. China.
Cell Biol Int. 2015 Oct;39(10):1151-61. doi: 10.1002/cbin.10488. Epub 2015 Jun 18.
Tooth loss is presently a global epidemic and tooth regeneration is thought to be a feasible and ideal treatment approach. Choice of cell source is a primary concern in tooth regeneration. In this study, the odontogenic differentiation potential of two non-dental-derived stem cells, adipose-derived stromal cells (ADSCs) and bone marrow-derived stromal cells (BMSCs), were evaluated both in vitro and in vivo. ADSCs and BMSCs were induced in vitro in the presence of tooth germ cell-conditioned medium (TGC-CM) prior to implantation into the omentum majus of rats, in combination with inactivated dentin matrix (IDM). Real-time quantitative polymerase chain reaction (RT-qPCR) was used to detect the mRNA expression levels of odontogenic-related genes. Immunofluorescence and immunohistochemical assays were used to detect the protein levels of odontogenic-specific genes, such as DSP and DMP-1 both in vitro and in vivo. The results suggest that both ADSCs and BMSCs have odontogenic differentiation potential. However, the odontogenic potential of BMSCs was greater compared with ADSCs, showing that BMSCs are a more appropriate cell source for tooth regeneration.
牙齿缺失目前是一种全球流行的疾病,牙齿再生被认为是一种可行且理想的治疗方法。细胞来源的选择是牙齿再生中的首要关注点。在本研究中,对两种非牙齿来源的干细胞,即脂肪来源的基质细胞(ADSCs)和骨髓来源的基质细胞(BMSCs)的牙源性分化潜能进行了体内和体外评估。在植入大鼠大网膜之前,将ADSCs和BMSCs在牙胚细胞条件培养基(TGC-CM)存在的情况下于体外进行诱导,并与灭活的牙本质基质(IDM)相结合。使用实时定量聚合酶链反应(RT-qPCR)检测牙源性相关基因的mRNA表达水平。免疫荧光和免疫组织化学分析用于在体内和体外检测牙源性特异性基因(如DSP和DMP-1)的蛋白质水平。结果表明,ADSCs和BMSCs均具有牙源性分化潜能。然而,与ADSCs相比,BMSCs的牙源性潜能更大,表明BMSCs是更适合用于牙齿再生的细胞来源。