Cooperative roles of BDNF expression in neurons and Schwann cells are modulated by exercise to facilitate nerve regeneration

• Type of Material: Article
• Authors: Jennifer C. Wilhelm, Emory University; Mei Xu, Philadelphia College of Osteopathic Medicine; Delia Cucoranu, Emory University; Sarah Chmielewski, Philadelphia College of Osteopathic Medicine; Tiffany Holmes, Philadelphia College of Osteopathic Medicine; Kelly (Shukkwan) Lau, Philadelphia College of Osteopathic Medicine; Gary Bassell, Emory University; Arthur W English, Emory University
• Language: English
• Date: 2012-04-04
• Publisher: Lippincott, Williams & Wilkins
• Publication Version: Final Published Version
• Copyright Statement: ©2012 the authors.
• Final Published Version (URL): http://dx.doi.org/10.1523/JNEUROSCI.1411-11.2012
• Title of Journal or Parent Work: Journal of Neuroscience Nursing
• ISSN: 0888-0395
• Volume: 32
• Issue: 14
• Start Page: 5002
• End Page: 5009
• Grant/Funding Information: This work was funded by Grants NS057190 (AWE), K12GM000680 (JCW), and HD055835 (GJB).
• Keywords: Life Sciences & Biomedicine; MOUSE; CRE; AXON REGENERATION; Science & Technology; TRANSGENIC MICE; PERIPHERAL-NERVES; MESSENGER-RNAS; RECEPTORS; Neurosciences; SCIATIC-NERVE; LOCALIZATION; Neurosciences & Neurology; TRKB
• Research Categories: Biology, Neuroscience; Biology, Cell; Biology, Anatomy

Abstract

After peripheral nerve injury, neurotrophins play a key role in the regeneration of damaged axons that can be augmented by exercise, although the distinct roles played by neurons and Schwann cells are unclear. In this study, we evaluated the requirement for the neurotrophin, brain-derived neurotrophic factor (BDNF), in neurons and Schwann cells for the regeneration of peripheral axons after injury. Common fibular or tibial nerves in thy-1-YFP-H mice were cut bilaterally and repaired using a graft of the same nerve from transgenic mice lacking BDNF in Schwann cells (BDNF-/-) or wild-type mice (WT). Two weeks postrepair, axonal regeneration into BDNF-/-grafts was markedly less thanWTgrafts, emphasizing the importance of Schwann cell BDNF. Nerve regeneration was enhanced by treadmill training posttransection, regardless of the BDNF content of the nerve graft. We further tested the hypothesis that traininginduced increases in BDNF in neurons allow regenerating axons to overcome a lack of BDNF expression in cells in the pathway through which they regenerate. Nerves in mice lacking BDNF in YFP+neurons (SLICK) were cut and repaired with BDNF-/-and WT nerves. SLICK axons lacking BDNF did not regenerate into grafts lacking Schwann cell BDNF. Treadmill training could not rescue the regeneration into BDNF-/-grafts if the neurons also lacked BDNF. Both Schwann cell- and neuron-derived BDNF are thus important for axon regeneration in cut peripheral nerves.