Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/79438
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Critical role of p38 MAPK for regeneration of the sciatic nerve following crush injury in vivo
Author: Kato, N.
Matsumoto, M.
Kogawa, M.
Atkins, G.
Findlay, D.
Fujikawa, T.
Oda, H.
Ogata, M.
Citation: Journal of Neuroinflammation, 2013; 10(1):1-13
Publisher: BioMed Central Ltd.
Issue Date: 2013
ISSN: 1742-2094
1742-2094
Statement of
Responsibility: 
Naoki Kato, Masahito Matsumoto, Masakazu Kogawa, Gerald J Atkins, David M Findlay, Takahiko Fujikawa, Hiromi Oda and Masato Ogata
Abstract: BACKGROUND 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. METHODS 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. RESULTS 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. CONCLUSIONS 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.
Keywords: P38 MAPK; Nerve regeneration; Crush injury; Inflammatory cytokines; TNF-α; IL-1β; Mutant mice; In vivo
Rights: © 2013 Kato et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
RMID: 0020125631
DOI: 10.1186/1742-2094-10-1
Appears in Collections:Orthopaedics and Trauma publications

Files in This Item:
File Description SizeFormat 
hdl_79438.pdfPublished version3.28 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.