Abstract

Previously, we showed silicone nerve conduits containing a vascular bundle and decellularized allogenic basal laminae (DABLs) seeded with bone marrow-derived mesenchymal stem cells (BMSCs) demonstrated successful nerve regeneration. Nerve conduits should be flexible and biodegradable for clinical use. In the current study, we used nerve conduits made of polyglycoric acid (PGA) fiber mesh, which is flexible, biodegradable and capillary-permeable. DABLs were created using chemical surfactants to remove almost all cell debris. In part 1, capillary infiltration capability of the PGA tube was examined. Capillary infiltration into regenerated neural tissue was compared between the PGA tube with blood vessels attached extratubularly (extratubularly vascularized tube) and that containing blood vessels intratubularly (intratubularly vascularized tube). No significant difference was found in capillary formation or nerve regeneration between these two tubes. In part 2, a 20 mm gap created in a rat sciatic nerve model was bridged using the extratubularly vascularized PGA tube containing the DABLs with implantation of isogenic cultured BMSCs (TubeC+ group), that containing the DABLs without implantation of the BMSCs (TubeC- group), and 20 mm-long fresh autologous nerve graft (Auto group). Nerve regeneration in these three groups was assessed electrophysiologically and histomorphometrically. At 24 weeks, there was no significant difference in any electrophysiological parameters between TubeC+ and Auto groups, although all histological parameters in Auto group were significantly greater than those in TubeC+ and TubeC- groups, and TubeC+ group demonstrated significant better nerve regeneration than TubeC- group. The transplanted DABLs showed no signs of immunological rejection and some transplanted BMSCs were differentiated into cells with Schwann cell-like phenotype, which might have promoted nerve regeneration within the conduit. This study indicated that the TubeC+ nerve conduit may become an alternative to nerve autograft.

Highlights

  • Autologous nerve grafting is a gold standard for repair of peripheral nerve deficits

  • Comparison of nerve regeneration through extratubularly vascularized polyglycoric acid (PGA) tubes containing DABLs seeded with bone marrow-derived mesenchymal stem cells (BMSCs) (TubeC+ group), extratubularly vascularized PGA tubes containing DABLs without BMSC transplantation (TubeC- group) and fresh autologous nerve segments (Auto group) in rat sciatic nerve with a 20mm deficit. 2.2.2.1 Animals

  • Because no nerve regeneration was found within the tube without vascularity (N-tube group), the vascularity supplied by nerve stumps attached to the either end of the tube is not enough to regenerate axons through a water-permeable nerve conduit even though the interstump gap was only 5mm in rat sciatic nerves

Read more

Summary

Introduction

Autologous nerve grafting is a gold standard for repair of peripheral nerve deficits. Kaizawa et al demonstrated excellent nerve regeneration through a silicone tube containing blood vessels and decellularized allogenic nerve basal laminae (DABLs) seeded with isogenic bone marrow-derived mesenchymal stem cells (BMSCs) in the tubular lumen using a rat sciatic nerve model with a 20 mm interstump gap [2]. They mentioned that the DABLs showed no signs of immunological rejection and functioned as a scaffold for nerve fiber extension, Schwann cell migration and transplanted BMSC retention. From the clinical point of view, the wall of nerve conduits should be flexible to tolerate the joint motion, biodegradable and capable of capillary infiltration

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call