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Cell Proliferation
Article . 2015 . Peer-reviewed
License: Wiley Online Library User Agreement
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Cell Proliferation
Article
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HKU Scholars Hub
Article . 2015
Data sources: HKU Scholars Hub
HKU Scholars Hub
Article . 2016
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Stimulation of EphB2/ephrin‐B1 signalling by tumour necrosis factor alpha in human dental pulp stem cells

Authors: Dissanayaka, WL; Green, DW; ZHU, L; Zhang, C;

Stimulation of EphB2/ephrin‐B1 signalling by tumour necrosis factor alpha in human dental pulp stem cells

Abstract

AbstractObjectivesThe aim of this study was to investigate whether in vitro stimulation of dental pulp stem cells (DPSCs) by tumour necrosis factor alpha (TNF‐α) would induce secretion of EphB2/ephrin‐B1 signalling.Materials and methodsDental pulp stem cells isolated from human dental pulp were treated with TNF‐α (5–100 ng/ml) over 2–48 h. EphB2/ephrin‐B1 mRNA and protein levels were measured by real‐time polymerase chain reaction (RT‐PCR) and western blot analysis respectively. Additionally, DPSCs were pre‐incubated with TNF‐α receptor neutralizing antibodies or infected with nuclear factor‐kappa B (NF‐ĸB) inhibitor, p38 MAPK inhibitor, Jun N‐terminal kinase (JNK) inhibitor and MEK inhibitor before TNF‐α treatment. Results were analysed by one‐way ANOVA.ResultsTumour necrosis factor alpha increased EphB2 mRNA expression in DPSCs at concentrations up to 20 ng/ml and ephrin‐B1 at concentrations up to 40 ng/ml (P < 0.05). Its mRNA expression reached maximum at 24 h when treated with TNF‐α at 20 ng/ml (P < 0.05). EphB2/ephrin‐B1 protein expression levels were high at 16 and 24 h as shown by western blotting. Neutralizing antibodies for TNFR1/2 receptors down‐regulated EphB2/ephrin‐B1 mRNA expression (P < 0.05) and ephrin‐B1 protein expression, but not EphB2 protein expression. JNK‐inhibitor inhibited EphB2 mRNA expression only (P < 0.05).ConclusionsEphB2/ephrin‐B1 were invoked in DPSCs with TNF‐α treatment via the JNK‐dependent pathway, but not NF‐ĸB, p38 MAPK or MEK signalling.

Countries
China (People's Republic of), Korea (Republic of), Korea (Republic of)
Related Organizations
Keywords

Adult, Ephrin-B1/genetics, Adolescent, MAP Kinase Signaling System, Receptor, EphB2, Cells, 610, Ephrin-B1, p38 Mitogen-Activated Protein Kinases, Antibodies, Ephrin-B1/metabolism*, Young Adult, Tumor Necrosis Factor-alpha/pharmacology*, Receptors, Humans, Receptors, Tumor Necrosis Factor, Type II, Antibodies/immunology, Cells, Cultured, Dental Pulp, Mitogen-Activated Protein Kinase Kinases, Ephrin-B1/secretion, Cultured, Mitogen-Activated Protein Kinase Kinases/antagonists & inhibitors, Tumor Necrosis Factor-alpha, Stem Cells, JNK Mitogen-Activated Protein Kinases, NF-kappa B, JNK Mitogen-Activated Protein Kinases/antagonists & inhibitors, Type II/metabolism, NF-kappa B/antagonists & inhibitors, Tumor Necrosis Factor-alpha/immunology, Stem Cells/cytology*, Receptors, Tumor Necrosis Factor, Type I, EphB2/secretion, Dental Pulp/cytology*, EphB2/genetics, Type I/metabolism, EphB2/metabolism*, Tumor Necrosis Factor, p38 Mitogen-Activated Protein Kinases/antagonists & inhibitors, Receptor

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
8
Top 10%
Average
Top 10%
Green
gold