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October 12, 2010Journal of Dental Research77 citations

TGF-β1 and FAK Regulate Periostin Expression in PDL Fibroblasts

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WWWei-Lun WenECEddy ChauLJLinda Jackson‐Boeters

Structured PICO

P
Population
Human periodontal ligament (PDL) in situ and PDL fibroblasts in vitro (including FAK-null fibroblasts)
I
Intervention
Uniaxial cyclic strain, transforming growth factor-beta1 (TGF-β1), and focal adhesion kinase (FAK) inhibition
C
Comparator
Unstimulated or control conditions
O
Outcome
Periostin protein expression and mRNA levelssurrogate

Periostin expression in human periodontal ligament fibroblasts is modulated by mechanical strain and TGF-β1 via FAK-dependent pathways.

Abstract

Recently identified as a key component of the murine periodontal ligament (PDL), periostin has been implicated in the regulation of collagen fibrillogenesis and fibroblast differentiation. We investigated whether periostin protein is expressed in the human PDL in situ and the mechanisms regulating periostin expression in PDL fibroblasts in vitro. With immunohistochemistry, periostin protein was identified in the PDL, with expression lower in teeth with reduced occlusal loading. In vitro application of uniaxial cyclic strain to PDL fibroblasts elevated periostin mRNA levels, depending on the age of the patient. Treatment with transforming growth factor-beta1 (TGF-β1) also significantly increased periostin mRNA levels, an effect attenuated by focal adhesion kinase (FAK) inhibition. FAK-null fibroblasts contained no detectable periostin mRNA, even after stimulation with cyclic strain. In conclusion, periostin protein is strongly expressed in the human PDL. In vitro, periostin mRNA levels are modulated by cyclic strain as well as TGF-β1 via FAK-dependent pathways.

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Cite This Study

Wen et al. (2010) studied this question.

synapsesocial.com/papers/6a8d2d692fb87b53917fe9ebhttps://doi.org/10.1177/0022034510378684
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