Institute of Stomatology, Nanjing Medical University, Nanjing, Jiangsu, China.
Histochem Cell Biol. 2012 Apr;137(4):513-25. doi: 10.1007/s00418-011-0908-x. Epub 2012 Jan 7.
Insulin-like growth factor 1 (IGF-1) is a potent mitogenic protein which can enhance the osteogenic differentiation of periodontal ligament (PDL) fibroblasts. However, it remains unclear whether IGF-1 can stimulate the osteogenic differentiation and osteogenesis of human periodontal ligament stem cells (PDLSCs). In this study, STRO-1(+) PDLSCs were isolated from human PDL tissues, treated with IGF-1, and their osteogenic capacity was investigated in vitro and in vivo. Dimethyl-thiazol-diphenyl tetrazolium bromide assay and flow cytometry results demonstrated that 10-200 ng/mL IGF-1 can stimulate the proliferation ability of PDLSCs and 100 ng/mL is the optimal concentration. Exogenous IGF-1 can modify the ultrastructure, enhance the alkaline phosphatase activity, the mineralization ability of PDLSCs, and increase the expression of osteogenic markers (runt-related transcription factor 2, osterix, and osteocalcin) at mRNA and protein levels. In vivo transplantation illustrated that IGF-1 treated implants generated more mineralized tissues, and presented stronger expression of RUNX2, OSX, and OCN than control group. Moreover, the expression of phosphor-ERK and phosphor-JNK in these stem cells was upregulated by IGF-1, indicating that MAPK signaling pathway was activated during the osteogenic differentiation of PDLSCs mediated by IGF-1. Together, the results showed that IGF-1 can promote the osteogenic differentiation and osteogenesis of STRO-1(+) PDLSCs via ERK and JNK MAPK pathway, suggesting that IGF-1 is a potent agent for stem cell-based periodontal tissue regeneration.
胰岛素样生长因子 1(IGF-1)是一种有效的有丝分裂原蛋白,可增强牙周膜(PDL)成纤维细胞的成骨分化。然而,目前尚不清楚 IGF-1 是否能刺激人牙周膜干细胞(PDLSCs)的成骨分化和骨生成。在本研究中,我们从人牙周组织中分离出 STRO-1(+)PDLSCs,用 IGF-1 处理,并在体外和体内研究其成骨能力。二甲基噻唑二苯基四唑溴盐(MTT)比色法和流式细胞术结果表明,10-200ng/mL 的 IGF-1 可刺激 PDLSCs 的增殖能力,100ng/mL 是最佳浓度。外源性 IGF-1 可改变 PDLSCs 的超微结构,增强碱性磷酸酶活性、矿化能力,并增加成骨标志物( runt 相关转录因子 2、osterix 和骨钙素)在 mRNA 和蛋白水平的表达。体内移植表明,IGF-1 处理的植入物产生了更多矿化组织,并且 RUNX2、OSX 和 OCN 的表达比对照组更强。此外,IGF-1 可上调这些干细胞中 ERK 和 JNK 磷酸化的表达,表明 MAPK 信号通路在 IGF-1 介导的 PDLSCs 成骨分化过程中被激活。综上所述,结果表明 IGF-1 可通过 ERK 和 JNK MAPK 通路促进 STRO-1(+)PDLSCs 的成骨分化和骨生成,提示 IGF-1 是一种促进基于干细胞的牙周组织再生的有效因子。