Mechanisms of Schwann cell plasticity involved in peripheral nerve repair after injury.
Gianluigi NoceraClaire JacobPublished in: Cellular and molecular life sciences : CMLS (2020)
The great plasticity of Schwann cells (SCs), the myelinating glia of the peripheral nervous system (PNS), is a critical feature in the context of peripheral nerve regeneration following traumatic injuries and peripheral neuropathies. After a nerve damage, SCs are rapidly activated by injury-induced signals and respond by entering the repair program. During the repair program, SCs undergo dynamic cell reprogramming and morphogenic changes aimed at promoting nerve regeneration and functional recovery. SCs convert into a repair phenotype, activate negative regulators of myelination and demyelinate the damaged nerve. Moreover, they express many genes typical of their immature state as well as numerous de-novo genes. These genes modulate and drive the regeneration process by promoting neuronal survival, damaged axon disintegration, myelin clearance, axonal regrowth and guidance to their former target, and by finally remyelinating the regenerated axon. Many signaling pathways, transcriptional regulators and epigenetic mechanisms regulate these events. In this review, we discuss the main steps of the repair program with a particular focus on the molecular mechanisms that regulate SC plasticity following peripheral nerve injury.
Keyphrases
- peripheral nerve
- stem cells
- quality improvement
- genome wide
- spinal cord injury
- gene expression
- induced apoptosis
- transcription factor
- single cell
- signaling pathway
- machine learning
- oxidative stress
- bioinformatics analysis
- cell death
- cell cycle arrest
- white matter
- genome wide identification
- wound healing
- blood brain barrier
- genome wide analysis
- epithelial mesenchymal transition
- cell proliferation
- heat shock
- brain injury
- cerebral ischemia
- heat shock protein