Tensile Stress-Activated and Exosome-Transferred YAP/TAZ-Notch Circuit Specifies Type H Endothelial Cell for Segmental Bone Regeneration.
Feng WangShanyu LiLingchi KongKai FengRongtai ZuoHanzhe ZhangYifan YuKunqi ZhangYuting CaoYimin ChaiQinglin KangJia XuPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
The Ilizarov technique has been continuously innovated to utilize tensile stress (TS) for inducing a bone development-like regenerative process, aiming to achieve skeletal elongation and reconstruction. However, it remains uncertain whether this distraction osteogenesis (DO) process induced by TS involves the pivotal coupling of angiogenesis and osteogenesis mediated by type H endothelial cells (THECs). In this study, it is demonstrated that the Ilizarov technique induces the formation of a metaphysis-like architecture composed of THECs, leading to segmental bone regeneration during the DO process. Mechanistically, cell-matrix interactions-mediated activation of yes-associated protein (YAP)/transcriptional co-activator with PDZ-binding motif (TAZ) transcriptionally upregulates the expression of Notch1 and Delta-like ligand 4, which act as direct positive regulators of THECs phenotype, in bone marrow endothelial cells (BMECs) upon TS stimulation. Simultaneously, the Notch intracellular domain enhances YAP/TAZ activity by transcriptionally upregulating YAP expression and stabilizing TAZ protein, thus establishing the YAP/TAZ-Notch circuit. Additionally, TS-stimulated BMECs secrete exosomes enriched with vital molecules in this positive feedback pathway, which can be utilized to promote segmental bone defect healing, mimicking the therapeutic effects of Ilizarov technique. The findings advance the understanding of TS-induced segmental bone regeneration and establish the foundation for innovative biological therapeutic strategies aimed at activating THECs.
Keyphrases
- bone regeneration
- endothelial cells
- high glucose
- mesenchymal stem cells
- bone marrow
- poor prognosis
- cell proliferation
- stem cells
- binding protein
- vascular endothelial growth factor
- cell therapy
- transcription factor
- long non coding rna
- gene expression
- immune response
- signaling pathway
- amino acid
- room temperature
- protein protein
- small molecule
- reactive oxygen species
- bone mineral density
- toll like receptor
- inflammatory response