These authors contributed equally to this work.
Protein expression profiling during wallerian degeneration after rat sciatic nerve injury
Article first published online: 19 JUN 2014
Copyright © 2013 Wiley Periodicals, Inc.
Muscle & Nerve
Volume 50, Issue 1, pages 73–78, July 2014
How to Cite
Li, M., Zhang, P., Guo, W., Li, H., Gu, X. and Yao, D. (2014), Protein expression profiling during wallerian degeneration after rat sciatic nerve injury. Muscle Nerve, 50: 73–78. doi: 10.1002/mus.24082
This research was supported by grants from: National Natural Science Foundation of China (Key Program, Grant No. 81130080); Scientific Research Foundation for Returned Scholars, Ministry of Education of China; Natural Science Foundation of Jiangsu Province (Grant No. BK2010282) and A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions, PAPD.
- Issue published online: 19 JUN 2014
- Article first published online: 19 JUN 2014
- Accepted manuscript online: 2 OCT 2013 06:09PM EST
- Manuscript Accepted: 12 SEP 2013
- Manuscript Revised: 19 AUG 2013
- Manuscript Received: 8 JAN 2013
- antibody arrays;
- bioinformatic analysis;
- protein expression;
- sciatic nerve;
- Wallerian degeneration
Introduction: Wallerian degeneration (WD) is an important area of research in modern neuroscience. Many protein expressions are regulated by differentially expressed genes in WD, but the precise mechanisms are elusive. Methods: In this study, we profiled differentially expressed proteins in WD after rat sciatic nerve injury using an antibody array. Results: Functional analysis positively identified cell proliferation, regulation of cell proliferation, and immune system processes. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis revealed molecular networks related mainly to cytokine–cytokine receptor interaction, the mitogen-activated proteinkinase (MAPK) signaling pathway, apoptosis, the toll-like receptor (TLR) signaling pathway, and the Janus kinase (Jak) - signal transducer and activator of transcription (STAT) signaling pathway. Interactions between these differential proteins were well established and regulated by the key factors transforming growth factor beta 1 (TGF-β1), toll-like receptor 4 (TLR4), Fas ligand (FasL), and 5′-AMP-activated protein kinase catalytic subunit alpha-1 (PRKAA1). Conclusions: These results provide information related to functional analysis of differentially expressed genes during WD. Muscle Nerve 50: 73–78, 2014