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ER stress-inducible ATF3 suppresses BMP2-induced ALP expression and activation in MC3T3-E1 cells
- Source :
- Biochemical and Biophysical Research Communications. 443:333-338
- Publication Year :
- 2014
- Publisher :
- Elsevier BV, 2014.
-
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.
- Subjects :
- musculoskeletal diseases
Biophysics
Activating transcription factor
Bone Morphogenetic Protein 2
Biochemistry
Bone morphogenetic protein 2
Cell Line
Mice
chemistry.chemical_compound
Osteogenesis
Gene expression
medicine
Animals
Humans
Molecular Biology
CAMP response element binding
Adaptor Proteins, Signal Transducing
Activating Transcription Factor 3
Osteoblasts
Chemistry
Endoplasmic reticulum
Membrane Proteins
Cell Differentiation
Osteoblast
Cell Biology
Tunicamycin
Endoplasmic Reticulum Stress
Molecular biology
medicine.anatomical_structure
Gene Expression Regulation
Unfolded protein response
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 443
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....4399a88171f75ec9d52fa471c9c6afcd
- Full Text :
- https://doi.org/10.1016/j.bbrc.2013.11.121