| First Author | Wang X | Year | 2015 |
| Journal | Cell Tissue Res | Volume | 362 |
| Issue | 2 | Pages | 317-30 |
| PubMed ID | 26077927 | Mgi Jnum | J:309234 |
| Mgi Id | MGI:6757381 | Doi | 10.1007/s00441-015-2219-3 |
| Citation | Wang X, et al. (2015) Growth/differentiation factor-15 and its role in peripheral nervous system lesion and regeneration. Cell Tissue Res 362(2):317-30 |
| abstractText | Growth/differentiation factor-15 (GDF-15) is a distant member of the transforming growth factor beta (TGF-beta) superfamily. It is widely distributed in the nervous system, where it has been shown to play an important role in neuronal maintenance. The present study investigates the role of endogenous GDF-15 in sciatic nerve (SN) lesions using wild-type (WT) and GDF-15 knock-out (KO) mice. SN of 5-6-month-old mice were crushed or transected. Dorsal root ganglia (DRG) and nerve tissue were analyzed at different time points from 6 h to 9 weeks post-lesion. Both crush and transection induced GDF-15 mRNA and protein in the distal portion of the nerve, with a peak at day 7. DRG neuron death did not significantly differ between the genotypes; similarly, remyelination of regenerating axons was not affected by the genotype. Alternative macrophage activation and macrophage recruitment were more pronounced in the KO nerve. Protrusion speed of axons was similar in the two genotypes but WT axons showed better maturation, as indicated by larger caliber at 9 weeks. Furthermore, the regenerated WT nerve showed better performance in the electromyography test, indicating better functional recovery. We conclude that endogenous GDF-15 is beneficial for axon regeneration following SN crush. |
