Comparative gene expression profiling reveals the mechanisms of axon regeneration
- PMID: 33248003
- DOI: 10.1111/febs.15646
Comparative gene expression profiling reveals the mechanisms of axon regeneration
Abstract
Axons are vulnerable to injury, potentially leading to degeneration or neuronal death. While neurons in the central nervous system fail to regenerate, neurons in the peripheral nervous system are known to regenerate. Since it has been shown that injury-response signal transduction is mediated by gene expression changes, expression profiling is a useful tool to understand the molecular mechanisms of regeneration. Axon regeneration is regulated by injury-responsive genes induced in both neurons and their surrounding non-neuronal cells. Thus, an experimental setup for the comparative analysis between regenerative and nonregenerative conditions is essential to identify ideal targets for the promotion of regeneration-associated genes and to understand the mechanisms of axon regeneration. Here, we review the original research that shows the key factors regulating axon regeneration, in particular by using comparative gene expression profiling in diverse systems.
Keywords: axon regeneration; comparative analysis; differential gene expression; gene expression profiling; nerve injury; transcriptome.
© 2020 Federation of European Biochemical Societies.
References
-
- Smith DS & Skene JH (1997) A transcription-dependent switch controls competence of adult neurons for distinct modes of axon growth. J Neurosci 17, 646-658.
-
- Tonge D, Chan K, Zhu N, Panjwani A, Arno M, Lynham S, Ward M, Snape A & Pizzey J (2008) Enhancement of axonal regeneration by in vitro conditioning and its inhibition by cyclopentenone prostaglandins. J Cell Sci 121, 2565-2577.
-
- Fournier AE, GrandPre T & Strittmatter SM (2001) Identification of a receptor mediating Nogo-66 inhibition of axonal regeneration. Nature 409, 341-346.
-
- Schwab ME (2004) Nogo and axon regeneration. Curr Opin Neurobiol 14, 118-124.
-
- Yiu G & He Z (2006) Glial inhibition of CNS axon regeneration. Nat Rev Neurosci 7, 617-627.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources