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Piezo1 通过施旺细胞衰老促进周围神经纤维性瘢痕形成。

Piezo1 promotes peripheral nerve fibrotic scar formation through Schwann cell senescence.

机构信息

Department of Microsurgery, Trauma and Hand Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

Department of Medical Ultrasonics, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

出版信息

Neurosci Lett. 2024 Aug 10;837:137916. doi: 10.1016/j.neulet.2024.137916. Epub 2024 Jul 24.

Abstract

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.

摘要

周围神经损伤 (PNI) 后,损伤部位的长期愈合过程涉及胶原蛋白纤维的渐进积累和局部瘢痕组织的形成。神经内过多的瘢痕组织形成阻碍了神经修复的过程。在这项研究中,我们证明了神经损伤后瘢痕的形成会导致局部物理微环境的改变,特别是神经硬度的增加。最近的研究表明,Piezo1 在雪旺细胞 (SCs) 中的表达增加。我们的研究结果还表明 Piezo1 在SCs 中的表达及其与增殖和迁移抑制的关联。转录组数据表明 Piezo1 的激活导致与衰老相关的基因表达上调。GO 富集分析显示 TGF-β 途径的上调。总的来说,我们的研究强调了 Piezo1 诱导的信号转导调节 SC 衰老的潜力及其在外周神经周围纤维性瘢痕形成的病理生理学中的潜在意义。

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