Axon-dependent expression of YAP/TAZ mediates Schwann cell remyelination but not proliferation after nerve injury.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32436841.
- Also identified by DOI 10.7554/eLife.50138 and PMC identifier 7259960.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Previously we showed that YAP/TAZ promote not only proliferation but also differentiation of immature Schwann cells (SCs), thereby forming and maintaining the myelin sheath around peripheral axons (Grove et al., 2017). Here we show that YAP/TAZ are required for mature SCs to restore peripheral myelination, but not to proliferate, after nerve injury. We find that YAP/TAZ dramatically disappear from SCs of adult mice concurrent with axon degeneration after nerve injury. They reappear in SCs only if axons regenerate. YAP/TAZ ablation does not impair SC proliferation or transdifferentiation into growth promoting repair SCs. SCs lacking YAP/TAZ, however, fail to upregulate myelin-associated genes and completely fail to remyelinate regenerated axons. We also show that both YAP and TAZ are redundantly required for optimal remyelination. These findings suggest that axons regulate transcriptional activity of YAP/TAZ in adult SCs and that YAP/TAZ are essential for functional regeneration of peripheral nerve.
Medical subject headings
- Adaptor Proteins, Signal Transducing
- Cell Cycle Proteins
- Remyelination
- Schwann Cells
- Sciatic Nerve
- Trans-Activators