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Effects of vascular endothelial growth factor (VEGF) on MC3T3‐E1
Author(s) -
Tan YY,
Yang YQ,
Chai L,
Wong RWK,
Rabie ABM
Publication year - 2010
Publication title -
orthodontics and craniofacial research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.664
H-Index - 55
eISSN - 1601-6343
pISSN - 1601-6335
DOI - 10.1111/j.1601-6343.2010.01498.x
Subject(s) - vascular endothelial growth factor , vegf receptors , vascular endothelial growth factor a , vascular endothelial growth factor c , cancer research , medicine , biology
To cite this article:
Tan YY, Yang Y‐Q, Chai L, Wong RWK, Rabie ABM:
Effects of vascular endothelial growth factor (VEGF) on MC3T3‐E1
Orthod Craniofac Res 2010; 13 :223–228 Structured Abstract Osteogenesis and angiogenesis are closely correlated. Vascular endothelial growth factor (VEGF) is believed to play a critical role in skeletal development. Authors – Tan YY, Yang Y‐Q, Chai L, Wong RWK, Rabie ABM Objective – To investigate whether VEGF has direct effects on bone cells activities and to better understand how VEGF promotes bone remodeling. Materials and Methods – MC3T3‐E1 cell line was cultured with and without VEGF in vitro . The cells in both control and test groups were collected at different culture time points of 24, 48 and 72 h. Real‐time polymerase chain reaction (qPCR) was carried out to quantify the mRNA expression of VEGF receptor (VEGFR2), alkaline phosphatase (ALP) and osteocalcin (OCN), osteoprotegerin (OPG) and receptor activator of nuclear factor kappa β ligand (RANKL). Results – The expression of VEGFR2 significantly increased by 53% at 24 h and remained increased by 8% at 72 h compared to control ( p < 0.05). ALP showed an early increase by 73% at 24 h ( p < 0.001), but dropped by 14 and 41% at 48 and 72 h, respectively ( p < 0.05). OCN was down‐regulated by 41% at 24 h but then up‐regulated by 149% at 72 h ( p < 0.001). The expression of OPG significantly decreased by 7% at 24 h ( p < 0.001) while dramatically increased by 133% at 72 h ( p < 0.001). RANKL remained unchanged at all three time points ( p > 0.05). Conclusion – VEGF promotes bone remodeling by direct effects on osteoblastic cells via regulating gene expression of ALP, OCN, and OPG through VEGFR2 signaling pathway.