Differential Impact of Fluid Shear Stress and YAP/TAZ on BMP/TGF-β Induced Osteogenic Target Genes.
Maria ReichenbachPaul-Lennard MendezCarolina da Silva MadalenoVladimir UgoretsPaul RikeitStefan BoernoJerome JatzlauPetra KnausPublished in: Advanced biology (2021)
Bone is a remarkable dynamic structure, which integrates mechanical and biochemical signaling inputs. Interstitial fluid in the intramedullary space transmits signals derived from compression-induced fluid shear stress (FSS) to stimulate osteoblasts for bone formation. Using a flow system and human osteoblasts, this study demonstrates how BMP/TGF-β signaling integrates stimuli derived from FSS and YAP/TAZ and confirms these findings by transcriptome analyses. Here, FSS positively affects the phosphorylation of both SMAD1/5 and SMAD2/3, the respective BMP- and TGFβ-R-SMADs. Increase in phosphorylated SMAD1/5 levels affects distinct target genes, which are susceptible to low levels of phosphorylated SMADs (such as ID1-3) or dependent on high levels of phosphorylated SMAD1/5 (NOG, noggin). Thus, FSS lowers the threshold for genes dependent on high levels of phosphorylated SMAD1/5 when less BMP is available. While the impact of FSS on direct BMP target genes is independent of YAP/TAZ, FSS acts cooperatively with YAP/TAZ on TGF-β target genes, which are shared by both pathways (such as CTGF). As mechanical stimuli are key in bone regeneration, their crosstalk to biochemical signaling pathways such as BMP and TGF-β and YAP/TAZ acts on different levels, which allows now to think about new and more specified intervention strategies for age-related bone loss.
Keyphrases
- transforming growth factor
- bone regeneration
- epithelial mesenchymal transition
- mesenchymal stem cells
- genome wide
- genome wide identification
- bone loss
- bioinformatics analysis
- signaling pathway
- randomized controlled trial
- bone marrow
- endothelial cells
- diabetic rats
- gene expression
- dna methylation
- drug induced
- oxidative stress
- transcription factor
- cell proliferation
- endoplasmic reticulum stress