Ye Guo, Li Conghua, Xiang Xuerong, Chen Chu, Zhang Ruyi, Yang Xia, Yu Xuesong, Wang Jinhua, Wang Lan, Shi Qiong, Weng Yaguang
1. Chongqing key Laboratory for Oral Diseases and Biomedical Sciences, Chongqing 401147, China ; 2. The Affiliated Hospital of Stomatology, Chongqing Medical University, Chongqing 401147, China.
3. Department of Laboratory Medicine, M.O.E. Key Laboratory of Laboratory Medicine Diagnostics, Chongqing Medical University, Chongqing 400016, China.
Int J Med Sci. 2014 Aug 6;11(10):1065-72. doi: 10.7150/ijms.8473. eCollection 2014.
Periodontal ligament stem cells (PDLSCs) with bone morphogenic ability are used to treat diseases such as periodontitis. Their treatment potential is increased when used in combination with proteins that induce osteogenic differentiation. For example, bone morphogenetic protein-9 (BMP9) has been found to have potent osteogenic activity. In the present study, PDLSCs were isolated from human periodontal membrane and infected with recombinant adenoviruses expressing BMP9 (Ad-BMP9). Levels of osteogenic markers such as runt-related transcription factor 2 (Runx2), alkaline phosphatase (ALP), osteopontin (OPN), and osteocalcin (OCN) as well as mineralization ability were measured. The results showed that BMP9 promoted bone formation of PDLSCs. In other experiments, SB203580 and PD98059, which are inhibitors of p38 and ERK1/2, respectively, were used to determine if these kinases are involved in the osteogenic differentiation process. The resulting protein expression profiles and osteogenic markers of PDLSCs revealed that the mitogen-activated protein kinase (MAPK) signaling pathway might play an important role in the process of BMP9-induced osteogenic differentiation of PDLSCs.
具有骨形成能力的牙周膜干细胞(PDLSCs)被用于治疗诸如牙周炎等疾病。当与诱导成骨分化的蛋白质联合使用时,它们的治疗潜力会增加。例如,已发现骨形态发生蛋白9(BMP9)具有强大的成骨活性。在本研究中,从人牙周膜中分离出PDLSCs,并感染表达BMP9的重组腺病毒(Ad-BMP9)。检测了成骨标志物如 runt相关转录因子2(Runx2)、碱性磷酸酶(ALP)、骨桥蛋白(OPN)和骨钙素(OCN)的水平以及矿化能力。结果表明,BMP9促进了PDLSCs的骨形成。在其他实验中,分别作为p38和ERK1/2抑制剂的SB203580和PD98059被用于确定这些激酶是否参与成骨分化过程。PDLSCs的蛋白质表达谱和成骨标志物结果显示,丝裂原活化蛋白激酶(MAPK)信号通路可能在BMP9诱导的PDLSCs成骨分化过程中发挥重要作用。