Enhanced peripheral nerve regeneration by mechano-electrical stimulation

• Published in: npj Regenerative medicine Vol. 8; no. 1; p. 57
• Main Authors: Tai, Youyi, Tonmoy, Thamidul Islam, Win, Shwe, Brinkley, Natasha T., Park, B. Hyle, Nam, Jin
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 17.10.2023; Nature Publishing Group; Nature Portfolio
• Subjects: 631/378/1687; 631/378/1959; 631/61/490; 692/308/2778; Biomaterials; Biomedical and Life Sciences; Biomedicine; Cell Biology; Immunology; Injuries; Morphology; Regenerative medicine; Regenerative Medicine/Tissue Engineering; Stem Cells; Tomography
• ISSN: 2057-3995; 2057-3995
• DOI: 10.1038/s41536-023-00334-y

To address limitations in current approaches for treating large peripheral nerve defects, the presented study evaluated the feasibility of functional material-mediated physical stimuli on peripheral nerve regeneration. Electrospun piezoelectric poly(vinylidene fluoride-trifluoroethylene) nanofibers were utilized to deliver mechanical actuation-activated electrical stimulation to nerve cells/tissues in a non-invasive manner. Using morphologically and piezoelectrically optimized nanofibers for neurite extension and Schwann cell maturation based on in vitro experiments, piezoelectric nerve conduits were synthesized and implanted in a rat sciatic nerve transection model to bridge a critical-sized sciatic nerve defect (15 mm). A therapeutic shockwave system was utilized to periodically activate the piezoelectric effect of the implanted nerve conduit on demand. The piezoelectric nerve conduit-mediated mechano-electrical stimulation (MES) induced enhanced peripheral nerve regeneration, resulting in full axon reconnection with myelin regeneration from the proximal to the distal ends over the critical-sized nerve gap. In comparison, a control group, in which the implanted piezoelectric conduits were not activated in vivo, failed to exhibit such nerve regeneration. In addition, at both proximal and distal ends of the implanted conduits, a decreased number of damaged myelination (ovoids), an increased number of myelinated nerves, and a larger axonal diameter were observed under the MES condition as compared to the control condition. Furthermore, unlike the control group, the MES condition exhibited a superior functional nerve recovery, assessed by walking track analysis and polarization-sensitive optical coherence tomography, demonstrating the significant potential of the piezoelectric conduit-based physical stimulation approach for the treatment of peripheral nerve injury.