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Critical role of p38 MAPK for regeneration of the sciatic nerve following crush injury in vivo

Naoki Kato12*, Masahito Matsumoto34, Masakazu Kogawa35, Gerald J Atkins5, David M Findlay5, Takahiko Fujikawa6, Hiromi Oda1 and Masato Ogata6

Author Affiliations

1 Department of Orthopaedic Surgery, Saitama Medical University, Saitama, Japan

2 Department of Orthopaedic Surgery, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe City, Saitama, 350-8550, Japan

3 Department of Molecular Biology, Saitama Medical University, Saitama, Japan

4 Division of Functional Genomics & Systems Medicine, Research Center of Genomic Medicine, Saitama Medical University, Saitama, Japan

5 Discipline of Orthopaedics and Trauma, The University of Adelaide, Adelaide, Australia

6 Department of Biochemistry, Mie University School of Medicine, Mie, Japan

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Journal of Neuroinflammation 2013, 10:1  doi:10.1186/1742-2094-10-1

Published: 3 January 2013



The physiological function of p38α, which is an isoform of p38 MAPK, has been investigated previously in several studies using pharmacological inhibitors. However, the results regarding whether p38α promotes or inhibits nerve regeneration in vivo have been controversial.


We generated novel p38α mutant mice (sem mice) with a point mutation in the region encoding the p38α substrate-docking-site, which serves as a limited loss-of-function model of p38α. In the present study, we utilized sem mice and wild-type littermates (wt mice) to investigate the physiological role of p38α in nerve regeneration following crush injuries.


At four weeks after crush injury, the average axon diameter and the average axon area in sem mice were significantly smaller than those in wt mice. The average myelin sheath thickness in sem mice was reduced compared to wt mice, but no significant difference was observed in the G-ratio between the two groups. The sciatic functional index value demonstrated that functional nerve recovery in sem mice following crush injury was delayed, which is consistent with the histological findings. To investigate the underlying mechanisms of these findings, we examined inflammatory responses of the sciatic nerve by immunohistochemistry and western blotting. At an early phase following crush injury, sem mice showed remarkably lower expression of inflammatory cytokines, such as TNF-α and IL-1β, than wt mice. The expression of Caspase-3 and Tenascin-C were also lower in sem mice. Conversely, at a late phase of the response, sem mice showed considerably higher expression of TNF-α and of IL-1β with lower expression of S-100 than wt mice.


This is the first study of the physiological role of p38 MAPK in nerve regeneration that does not rely on the use of pharmacological inhibitors. Our results indicate that p38α insufficiency may cause an inflammatory disorder, resulting in a delay of histological and functional nerve recovery following crush injury. We conclude that p38 MAPK has an important physiological role in nerve regeneration and may be important for controlling both initiation of inflammation and recovery from nerve injury.

P38 MAPK; Nerve regeneration; Crush injury; Inflammatory cytokines; TNF-α; IL-1β; Mutant mice; In vivo