Mechanically-induced GDF15 Secretion by Periodontal Ligament Fibroblasts Regulates Osteogenic Transcription.
Judit SymmankSarah ZimmermannJutta GoldschmittEik SchiegnitzMichael WolfHeinrich WehrbeinCollin JacobsPublished in: Scientific reports (2019)
The alveolar bone provides structural support against compressive and tensile forces generated during mastication as well as during orthodontic treatment. To avoid abnormal alveolar bone resorption and tooth loss, a balanced bone turnover by bone-degrading osteoclasts and bone-generating osteoblasts is of great relevance. Unlike its contradictory role in regulating osteoclast and osteoblast cell differentiation, the TGF-β/BMP-family member GDF15 is well known for its important functions in the regulation of cell metabolism, as well as cell fate and survival in response to cellular stress. Here, we provide first evidence for a potential role of GDF15 in translating mechanical stimuli into cellular changes in immature osteoblasts. We detected enhanced levels of GDF15 in vivo in periodontal ligament cells after the simulation of tooth movement in rat model system as well as in vitro in mechanically stressed human periodontal ligament fibroblasts. Moreover, mechanical stimulation enhanced GDF15 secretion by periodontal ligament cells and the stimulation of human primary osteoblast with GDF15 in vitro resulted in an increased transcription of osteogenic marker genes like RUNX2, osteocalcin (OCN) and alkaline phosphatase (ALP). Together, the present data emphasize for the first time a potential function of GDF15 in regulating differentiation programs of immature osteoblasts according to mechanical stimulation.
Keyphrases
- bone mineral density
- bone loss
- bone regeneration
- mesenchymal stem cells
- induced apoptosis
- soft tissue
- postmenopausal women
- endothelial cells
- transcription factor
- cell cycle arrest
- bone marrow
- cell fate
- body composition
- gene expression
- induced pluripotent stem cells
- stem cells
- public health
- pluripotent stem cells
- dna methylation
- epithelial mesenchymal transition
- signaling pathway
- cell death
- transforming growth factor
- endoplasmic reticulum stress
- heat stress
- climate change