| First Author | Zhao K | Year | 2017 |
| Journal | J Neurosci | Volume | 37 |
| Issue | 13 | Pages | 3465-3477 |
| PubMed ID | 28213440 | Mgi Jnum | J:240545 |
| Mgi Id | MGI:5887149 | Doi | 10.1523/JNEUROSCI.2934-16.2017 |
| Citation | Zhao K, et al. (2017) Muscle Yap Is a Regulator of Neuromuscular Junction Formation and Regeneration. J Neurosci 37(13):3465-3477 |
| abstractText | Yes-associated protein (Yap) is a major effector of the Hippo pathway that regulates cell proliferation and differentiation during development and restricts tissue growth in adult animals. However, its role in synapse formation remains poorly understood. In this study, we characterized Yap's role in the formation of the neuromuscular junction (NMJ). In HSA-Yap-/- mice where Yap was mutated specifically in muscle cells, AChR clusters were smaller and were distributed in a broader region in the middle of muscle fibers, suggesting that muscle Yap is necessary for the size and location of AChR clusters. In addition, HSA-Yap-/- mice also exhibited remarkable presynaptic deficits. Many AChR clusters were not or less covered by nerve terminals; miniature endplate potential frequency was reduced, which was associated with an increase in paired-pulse facilitation, indicating structural and functional defects. In addition, muscle Yap mutation prevented reinnervation of denervated muscle fibers. Together, these observations indicate a role of muscle Yap in NMJ formation and regeneration. We found that beta-catenin was reduced in the cytoplasm and nucleus of mutant muscles, suggesting compromised beta-catenin signaling. Both NMJ formation and regeneration deficits of HSA-Yap-/- mice were ameliorated by inhibiting beta-catenin degradation, further corroborating a role of beta-catenin or Wnt-dependent signaling downstream of Yap to regulate NMJ formation and regeneration.SIGNIFICANCE STATEMENT This paper explored the role of Yes-associated protein (Yap) in neuromuscular junction (NMJ) formation and regeneration. Yap is a major effector of the Hippo pathway that regulates cell proliferation and differentiation during development and restricts tissue growth in adult animals. However, its role in synapse formation remains poorly understood. We provide evidence that muscle Yap mutation impairs both postsynaptic and presynaptic differentiation and function and inhibits NMJ regeneration after nerve injury, indicating a role of muscle Yap in these events. Further studies suggest compromised beta-catenin signaling as a potential mechanism. Both NMJ formation and regeneration deficits of HSA-Yap-/- mice were ameliorated by inhibiting beta-catenin degradation, corroborating a role of beta-catenin or Wnt-dependent signaling downstream of Yap to regulate NMJ formation and regeneration. |
