A novel model for the study of peripheral-nerve regeneration following common nerve injury paradigms

Terence M. Myckatyn, Susan E. Mackinnon, Daniel A. Hunter, Danielle Brakefield, Alexander Parsadanian

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Recent advances in molecular neurobiology include the development of transgenic mice that express genes encoding fluorescent proteins under neuron-specific promoters (XFP mice). These mice have been used in the field of developmental neurobiology, but use has expanded to include the study of peripheral-nerve axonal regeneration subsequent to crush or unrepaired transection injuries. This report presents a transgenic mouse, which differs from previously reported and commercially available mice, in that enhanced yellow fluorescent protein expression (EYFP) is driven by the human thyl promoter (hThyl). Motor and sensory peripheral nerves in these mice appear a bright yellow-green under fluorescent microscopy. This study tracks nerve regeneration in live animals using a serial imaging system. It also introduces a novel model for examining the clinically relevant nerve-injury paradigms of tibial nerve transection repaired with primary neurorrhaphy or graft, and end-to-side neurorrhaphy. Live-animal serial nerve imaging is compared with wet-mount fluorescent microscopy and histomorphometry in the same nerve specimens. The use of transgenic mice that strongly express EYFP in their peripheral neurons, coupled with serial nerve imaging, provide an important methodology for studying the heterogeneous nature of axonal elongation following peripheral-nerve injuries.

Original languageEnglish
Pages (from-to)533-544
Number of pages12
JournalJournal of reconstructive microsurgery
Volume20
Issue number7
DOIs
StatePublished - Oct 1 2004

Keywords

  • Neurorrhaphy
  • Serial imaging
  • Transgenic mice
  • Yellow fluorescent protein

Fingerprint

Dive into the research topics of 'A novel model for the study of peripheral-nerve regeneration following common nerve injury paradigms'. Together they form a unique fingerprint.

Cite this