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

Authors :
Yu, Yan
Mu, Jinquan
Fan, Zhipeng
Lei, Gang
Yan, Ming
Wang, Sainan
Tang, Chunbo
Wang, Zilu
Yu, Jinhua
Zhang, Guangdong
Source :
Histochemistry & Cell Biology; Apr2012, Vol. 137 Issue 4, p513-525, 13p, 2 Color Photographs, 1 Black and White Photograph, 1 Chart, 5 Graphs
Publication Year :
2012

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09486143
Volume :
137
Issue :
4
Database :
Complementary Index
Journal :
Histochemistry & Cell Biology
Publication Type :
Academic Journal
Accession number :
73463996
Full Text :
https://doi.org/10.1007/s00418-011-0908-x