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ER stress-inducible ATF3 suppresses BMP2-induced ALP expression and activation in MC3T3-E1 cells

  • Jae kyung Park
  • , Hoon Jang
  • , Seong Soo Hwang
  • , Eun Jung Kim
  • , Dong Ern Kim
  • , Keon Bong Oh
  • , Dae Jin Kwon
  • , Jeong Tae Koh
  • , Kumi Kimura
  • , Hiroshi Inoue
  • , Won Gu Jang*
  • , Jeong Woong Lee
  • *Corresponding author for this work
  • Korea Research Institute of Bioscience and Biotechnology
  • University of Science and Technology UST
  • Rural Development Administration
  • Chonnam National University
  • Kanazawa University
  • Daegu University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Endoplasmic reticulum (ER) stress suppresses osteoblast differentiation. Activating transcription factor (ATF) 3, a member of the ATF/cAMP response element-binding protein family of transcription factors, is induced by various stimuli including cytokines, hormones, DNA damage, and ER stress. However, the role of ATF3 in osteoblast differentiation has not been elucidated. Treatment with tunicamycin (TM), an ER stress inducer, increased ATF3 expression in the preosteoblast cell line, MC3T3-E1. Overexpression of ATF3 inhibited bone morphogenetic protein 2-stimulated expression and activation of alkaline phosphatase (ALP), an osteogenic marker. In addition, suppression of ALP expression by TM treatment was rescued by silencing of ATF3 using shRNA. Taken together, these data indicate that ATF3 is a novel negative regulator of osteoblast differentiation by specifically suppressing ALP gene expression in preosteoblasts.

Original languageEnglish
Pages (from-to)333-338
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume443
Issue number1
DOIs
StatePublished - 2014.01.3

Keywords

  • Activating transcription factor 3 (ATF3)

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