Abstract

Electrospinning can be used to mimic the architecture of an acellular nerve graft, combining microfibers for guidance, and pores for cellular infiltration. We made electrospun nerve guides, from polycaprolactone (PCL) or poly-L-lactic acid (PLLA), with aligned fibers along the insides of the channels and random fibers around them. We bridged a 10 mm rat sciatic nerve defect with the guides, and, in selected groups, added a cell transplant derived from autologous stromal vascular fraction (SVF). For control, we compared to hollow silicone tubes; or autologous nerve grafts. PCL nerve guides had a high degree of autotomy (8/43 rats), a negative indicator with respect to future usefulness, while PLLA supported axonal regeneration, but did not outperform autologous nerve grafts. Transplanted cells survived in the PLLA nerve guides, but axonal regeneration was not enhanced as compared to nerve guides alone. The inflammatory response was partially enhanced by the transplanted cells in PLLA nerve grafts; Schwann cells were poorly distributed compared to nerve guide without cells. Tailor-made electrospun nerve guides support axonal regeneration in vivo, and can act as vehicles for co-transplanted cells. Our results motivate further studies exploring novel nerve guides and the effect of stromal cell-derived factors on nerve generation.

Highlights

  • Electrospinning can be used to mimic the architecture of an acellular nerve graft, combining microfibers for guidance, and pores for cellular infiltration

  • The stromal vascular fraction (SVF) is obtained after enzymatic digestion of adipose tissue and elimination of floating mature adipocytes, and contains, among many other cell types, a fraction of adipose-derived stromal and stem cells (ASC)[11]

  • Polycaprolactone (PCL) and poly-L-lactic acid (PLLA), we investigated the in vivo performance up to 28 days in a rat model of sciatic nerve injury and reconstruction, and it’s potential to bridge a 10 mm nerve gap, and act as a cell delivery vehicle

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Summary

Introduction

Electrospinning can be used to mimic the architecture of an acellular nerve graft, combining microfibers for guidance, and pores for cellular infiltration. We bridged a 10 mm rat sciatic nerve defect with the guides, and, in selected groups, added a cell transplant derived from autologous stromal vascular fraction (SVF). Transplanted cells survived in the PLLA nerve guides, but axonal regeneration was not enhanced as compared to nerve guides alone. Recent studies have examined the addition of uncultured stromal vascular fraction (SVF) to hollow tubes and vessel grafts in attempts to improve peripheral nerve regeneration in rats[7,8,9,10]. Nanofibers may play a dual role for topical guidance as well as cell adhesion of transplanted cells Embracing these demands, electrospinning can be used to create fibers and 3D structures from biodegradable and biocompatible polymers, with an appealing range of possible applications in regenerative medicine[18,19]

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