AI Article Synopsis

  • The neuromuscular junction (NMJ) is made up of motor neurons, muscle fibers, and Schwann cells, which are crucial for its development.
  • Conditional inactivation of specific genes in Schwann cells in mice led to delayed NMJ maturation and muscle growth, mirroring symptoms of muscular dystrophy seen in neurofibromatosis type I.
  • Analysis of the affected Schwann cells revealed disrupted signaling pathways, particularly hyperactive RAS/PI3K/AKT/mTOR, indicating their critical role in NMJ and muscle development.

Article Abstract

The neuromuscular junction (NMJ) consists of three components, namely presynaptic motor neurons, postsynaptic muscle fibers and perisynaptic Schwann cells (PSCs). The role of Schwann cells (SCs) in regulating NMJ structural and functional development remains unclear. In this study, mice with conditional inactivation of () and (), specifically in SCs, resulted in delayed NMJ maturation that led to delayed muscle growth, recapitulating the muscular dystrophy condition observed in human neurofibromatosis type I syndrome (NF1) patients. Expression levels of NMJ development related molecules such as , , (), (), , (), , () and () were also downregulated. To further explore the molecular alterations in these SCs, NF1- and PTEN-related pathways were analyzed in mutant sciatic nerves. As expected, hyperactive RAS/PI3K/AKT/mTOR signaling pathways were identified, suggesting the importance of these pathways for NMJ development, and subsequent muscle maturation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325916PMC
http://dx.doi.org/10.1534/g3.118.200795DOI Listing

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