Tissue-engineered grafts exploit axon-facilitated axon regeneration and pathway protection to enable recovery after 5-cm nerve defects in pigs

Author:

Smith Douglas H.12ORCID,Burrell Justin C.134ORCID,Browne Kevin D.13,Katiyar Kritika S.123ORCID,Ezra Mindy I.1,Dutton John L.1,Morand Joseph P.1ORCID,Struzyna Laura A.134,Laimo Franco A.13ORCID,Chen H. Isaac13ORCID,Wolf John A.13ORCID,Kaplan Hilton M.5ORCID,Rosen Joseph M.6,Ledebur Harry C.2ORCID,Zager Eric L.1ORCID,Ali Zarina S.13ORCID,Cullen D. Kacy1234ORCID

Affiliation:

1. Center for Brain Injury and Repair, Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

2. Axonova Medical LLC, Philadelphia, PA, USA.

3. Center for Neurotrauma, Neurodegeneration and Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.

4. Department of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA, USA.

5. New Jersey Center for Biomaterials, Rutgers University, Piscataway, NJ, USA.

6. Division of Plastic Surgery, Dartmouth Hitchcock Medical Center, Dartmouth College, Lebanon, NH, USA.

Abstract

Functional restoration following major peripheral nerve injury (PNI) is challenging, given slow axon growth rates and eventual regenerative pathway degradation in the absence of axons. We are developing tissue-engineered nerve grafts (TENGs) to simultaneously “bridge” missing nerve segments and “babysit” regenerative capacity by providing living axons to guide host axons and maintain the distal pathway. TENGs were biofabricated using porcine neurons and “stretch-grown” axon tracts. TENG neurons survived and elicited axon-facilitated axon regeneration to accelerate regrowth across both short (1 cm) and long (5 cm) segmental nerve defects in pigs. TENG axons also closely interacted with host Schwann cells to maintain proregenerative capacity. TENGs drove regeneration across 5-cm defects in both motor and mixed motor-sensory nerves, resulting in dense axon regeneration and electrophysiological recovery at levels similar to autograft repairs. This approach of accelerating axon regeneration while maintaining the pathway for long-distance regeneration may achieve recovery after currently unrepairable PNIs.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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