After peripheral nerve injury (PNI), the long-term healing process at the injury site involves a progressive accumulation of collagen fibers and the development of localized scar tissue. Excessive formation of scar tissue within nerves hinders the process of nerve repair. In this study, we demonstrate that scar formation following nerve injury induces alterations in the local physical microenvironment, specifically an increase in nerve stiffness. Recent research has indicated heightened expression of Piezo1 in Schwann cells (SCs). Our findings also indicate Piezo1 expression in SCs and its association with suppressed proliferation and migration. Transcriptomic data suggests that activation of Piezo1 results in elevated expression of senescence-associated genes. GO enrichment analysis reveals upregulation of the TGF-β pathway. Overall, our study highlights the potential for Piezo1-induced signaling to regulate SC senescence and its potential significance in the pathophysiology of fibrotic scar formation surrounding peripheral nerves.
Keyphrases
- peripheral nerve
- poor prognosis
- wound healing
- dna damage
- endothelial cells
- single cell
- stem cells
- multiple sclerosis
- binding protein
- induced apoptosis
- stress induced
- cell proliferation
- systemic sclerosis
- physical activity
- mental health
- idiopathic pulmonary fibrosis
- machine learning
- transforming growth factor
- high glucose
- genome wide
- signaling pathway
- weight gain
- risk assessment
- oxidative stress
- electronic health record
- climate change
- cell therapy
- cell death