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YAP/TAZ initiate and maintain Schwann cell myelination.

Matthew GroveHyukmin KimMaryline SanterreAlexander J KrupkaSeung Baek HanJinbin ZhaiJennifer Y ChoRaehee ParkMichele HarrisSeonhee KimBassel E SawayaShin H KangMary F BarbeSeo-Hee ChoMichel A LemayYoung-Jin Son
Published in: eLife (2017)
Nuclear exclusion of the transcriptional regulators and potent oncoproteins, YAP/TAZ, is considered necessary for adult tissue homeostasis. Here we show that nuclear YAP/TAZ are essential regulators of peripheral nerve development and myelin maintenance. To proliferate, developing Schwann cells (SCs) require YAP/TAZ to enter S-phase and, without them, fail to generate sufficient SCs for timely axon sorting. To differentiate, SCs require YAP/TAZ to upregulate Krox20 and, without them, completely fail to myelinate, resulting in severe peripheral neuropathy. Remarkably, in adulthood, nuclear YAP/TAZ are selectively expressed by myelinating SCs, and conditional ablation results in severe peripheral demyelination and mouse death. YAP/TAZ regulate both developmental and adult myelination by driving TEAD1 to activate Krox20. Therefore, YAP/TAZ are crucial for SCs to myelinate developing nerve and to maintain myelinated nerve in adulthood. Our study also provides a new insight into the role of nuclear YAP/TAZ in homeostatic maintenance of an adult tissue.
Keyphrases
  • peripheral nerve
  • stem cells
  • cell therapy
  • cell proliferation
  • multiple sclerosis
  • mesenchymal stem cells
  • atrial fibrillation
  • signaling pathway
  • early life
  • optical coherence tomography