Activation of the Extracellular Signal-Regulated Kinase Signaling Is Critical for Human Umbilical Cord Mesenchymal Stem Cell Osteogenic Differentiation
Penn collection
Degree type
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Cell Differentiation
Humans
JNK Mitogen-Activated Protein Kinases
MAP Kinase Signaling System
Mesenchymal Stem Cell Transplantation
Mesenchymal Stromal Cells
Osteogenesis
p38 Mitogen-Activated Protein Kinases
Phosphorylation
Tissue Engineering
Umbilical Cord
1
4 diamino 1
4 bis(2 aminophenylthio) 2
3 dicyanobutadiene
alkaline phosphatase
bone sialoprotein
calcium
collagen type 1
mitogen activated protein kinase
mitogen activated protein kinase p38
osteocalcin
osteopontin
stress activated protein kinase
mitogen activated protein kinase p38
stress activated protein kinase
Article
bone development
bone regeneration
cell differentiation
controlled study
enzyme activation
gene expression
human umbilical cord mesenchymal stem cell
loss of function mutation
marker gene
mesenchymal stem cell
protein phosphorylation
signal transduction
tissue engineering
umbilical cord
biosynthesis
cell differentiation
cytology
genetics
human
mesenchymal stem cell transplantation
mesenchymal stroma cell
phosphorylation
transplantation
Dentistry
Oral and Maxillofacial Surgery
Orthodontics and Orthodontology
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Abstract
Human umbilical cord mesenchymal stem cells (hUCMSCs) are recognized as candidate progenitor cells for bone regeneration. However, the mechanism of hUCMSC osteogenesis remains unclear. In this study, we revealed that mitogen-activated protein kinases (MAPKs) signaling is involved in hUCMSC osteogenic differentiation in vitro. Particularly, the activation of c-Jun N-terminal kinases (JNK) and p38 signaling pathways maintained a consistent level in hUCMSCs through the entire 21-day osteogenic differentiation period. At the same time, the activation of extracellular signal-regulated kinases (ERK) signaling significantly increased from day 5, peaked at day 9, and declined thereafter. Moreover, gene profiling of osteogenic markers, alkaline phosphatase (ALP) activity measurement, and alizarin red staining demonstrated that the application of U0126, a specific inhibitor for ERK activation, completely prohibited hUCMSC osteogenic differentiation. However, when U0126 was removed from the culture at day 9, ERK activation and osteogenic differentiation of hUCMSCs were partially recovered. Together, these findings demonstrate that the activation of ERK signaling is essential for hUCMSC osteogenic differentiation, which points out the significance of ERK signaling pathway to regulate the osteogenic differentiation of hUCMSCs as an alternative cell source for bone tissue engineering. Copyright © 2016 Chen-Shuang Li et al.