Biofabrication and testing of a fully cellular nerve graft.

Biofabrication

Department of Physics and Astronomy, University of Missouri, Columbia, MO 65211, USA.

Published: December 2013

AI Article Synopsis

  • Ruptured nerves lead to serious quality-of-life issues, and the usual repair method involves using a patient's own tissue, which can have complications like infection.
  • Researchers developed a new method to create fully biological grafts made of cells and their secreted materials, using bioprinting technology.
  • Tests on rat models show that these biofabricated grafts promote nerve regeneration similarly to traditional autologous grafts and may provide a viable alternative for nerve repair.

Article Abstract

Rupture of a nerve is a debilitating injury with devastating consequences for the individual's quality of life. The gold standard of repair is the use of an autologous graft to bridge the severed nerve ends. Such repair however involves risks due to secondary surgery at the donor site and may result in morbidity and infection. Thus the clinical approach to repair often involves non-cellular solutions, grafts composed of synthetic or natural materials. Here we report on a novel approach to biofabricate fully biological grafts composed exclusively of cells and cell secreted material. To reproducibly and reliably build such grafts of composite geometry we use bioprinting. We test our grafts in a rat sciatic nerve injury model for both motor and sensory function. In particular we compare the regenerative capacity of the biofabricated grafts with that of autologous grafts and grafts made of hollow collagen tubes by measuring the compound action potential (for motor function) and the change in mean arterial blood pressure as consequence of electrically eliciting the somatic pressor reflex. Our results provide evidence that bioprinting is a promising approach to nerve graft fabrication and as a consequence to nerve regeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007150PMC
http://dx.doi.org/10.1088/1758-5082/5/4/045007DOI Listing

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