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Updated: Aug 27, 2026
Facial Nerve Axotomy in Mice: A Model to Study Motoneuron Response to Injury
Published on: February 23, 2015
[Expression of BDNF and FGF-2 following axotomy in rat facial motoneurons]
1Department of Otorhinolaryngology, First Affiliated Hospital of Henan Medical University, Zhengzhou 450052, China. qinzhb@371.net
Objective:
To study the expression and distribution of brain derived neurotrophic factor (BDNF) and fibroblast growth factor-2 (FGF-2) in normal facial motoneurons (FMNs) and in FMNs following axotomy.
Methods:
The right facial nerves were transected 6 mm distal to the stylomastoid foraman in adult Wistar rats except the normal group. Serial 20 microns cryosections were cut through the whole brainstems. Expressions of BDNF and FGF-2 mRNA as well as BDNF and FGF-2 protein were studied by in situ hybridization, immunohistochemistry and image analysis.
Results:
BDNF mRNA and its protein were observed in widespread areas of normal rat facial nucleus, and those increased 1 day after axotomy. In addition to neurons, glial cells were also stained. FGF-2 mRNA and its protein were mainly localized in normal FMNs of ventral facial nucleus. After axotomy, expression of FGF-2 mRNA started to up-regulate in FMNs at 7 days, however FGF-2 protein drastically reduced at 3 and 7 days.
Conclusion:
In addition to target-supporting, there may be BDNF autocrine and paracrine mechanisms as well as FGF-2 autocrine mechanisms in normal rat FMN. When target-derived BDNF is deprived, alternative sources of BDNF support may substitute immediately after axotomy. However, deprivating of target--derived FGF-2 may result in down-regulation of FGF-2 protein in adult rat FMNs at early stage after axotomy. These suggest that the exogenous FGF-2 might provide a supportive environment for the recovery of metabolism and function of FMNs at early stage following axotomy.
