Mechano-regulation of Wnt/β-Catenin signaling to control paraxial versus lateral mesoderm lineage bifurcation.
Tobias StrittmatterViktor HaellmanPaul ArgastPeter BuchmanAna Palma TeixeiraMartin FusseneggerPublished in: Biotechnology progress (2022)
Mechanical cues are involved in many biological processes, including embryonic development and patterning. For example, external mechanical forces (shear stress), lateral cell-cell interactions, and mechanical properties (stiffness and composition) of the extracellular matrix are thought to modulate Wnt signaling, which is a highly conserved pathway involved in regulating stem cell renewal, proliferation, and differentiation. In this work, we employed a customized higher-throughput shear stress induction device for the controlled application of mechanical stress to study the effects of shear stress on the differentiation of human induced pluripotent stem cells (hiPSCs) toward the three germ layers. We found that mechanical stress alters lineage commitment during ectoderm and mesoderm differentiation. We show that this effect correlates with reduced Wnt signaling, evaluated in terms of the promoter activity of an established TCF3-responsive promoter. Whole transcriptome sequencing and pathway enrichment analysis of the differentially expressed genes between hiPSC-derived mesoderm cells differentiated in the presence or absence of piston-induced shear stress confirmed that Wnt/β-catenin signaling is among the most affected developmental pathways. Furthermore, our results suggest that suitably programmed shear stress application could be used to selectively promote differentiation of hiPSCs to either lateral or paraxial mesoderm in commercially available media.
Keyphrases
- single cell
- pluripotent stem cells
- stem cells
- induced pluripotent stem cells
- extracellular matrix
- rna seq
- transcription factor
- dna methylation
- gene expression
- minimally invasive
- cell therapy
- cell proliferation
- induced apoptosis
- endothelial cells
- genome wide
- cell fate
- cancer therapy
- stress induced
- mesenchymal stem cells
- high glucose
- drug induced
- cell death