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胰岛素样生长因子 1 通过 ERK 和 JNK MAPK 通路增强人牙周膜干细胞的增殖和成骨分化。

Insulin-like growth factor 1 enhances the proliferation and osteogenic differentiation of human periodontal ligament stem cells via ERK and JNK MAPK pathways.

机构信息

Institute of Stomatology, Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

Histochem Cell Biol. 2012 Apr;137(4):513-25. doi: 10.1007/s00418-011-0908-x. Epub 2012 Jan 7.

Abstract

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.

摘要

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。

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