4.7 Article

The synaptosome-associated protein 23 (SNAP23) is necessary for proper myogenesis

Journal

FASEB JOURNAL
Volume 36, Issue 8, Pages -

Publisher

WILEY
DOI: 10.1096/fj.202101627RR

Keywords

IGF1; myogenesis; proliferation; secretion; SNAP23

Funding

  1. American Heart Association (AHA) [19CDA34660248]
  2. National Institutes of Health (NIH) [R01GM130866]
  3. March of Dimes Foundation (MDF) [5-FY18-36]
  4. National Science Foundation (NSF) [DGE-1650116]
  5. Nutrition Obesity Research Center, University of North Carolina (NORC) [P30-DK056350]
  6. Cancer Center Core Support Grant [P30 CA016086]
  7. National Institutes of Health (NIH)-NIGMS training award [R25GM089569, T32GM119999, 5T32GM007092]
  8. National Institutes of Health (NIAH)-NIAMS F31 predoctoral fellowship [AR077381-01A1]

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Vesicle-mediated transport is crucial for maintaining cellular homeostasis and proper signaling. This study reveals that the depletion of SNAP23 protein, which mediates vesicle docking and membrane fusion, impairs the differentiation of skeletal muscle cells. The researchers also identified the misregulation of exocytosis and decreased secretion of IGF1 in SNAP23-depleted cells, which is critical for muscle development and function. This work highlights the overlooked role of skeletal muscle as a secretory organ and contributes to our understanding of factors necessary for myogenesis.
Vesicle-mediated transport is necessary for maintaining cellular homeostasis and proper signaling. The synaptosome-associated protein 23 (SNAP23) is a member of the SNARE protein family and mediates the vesicle docking and membrane fusion steps of secretion during exocytosis. Skeletal muscle has been established as a secretory organ; however, the role of SNAP23 in the context of skeletal muscle development is still unknown. Here, we show that depletion of SNAP23 in C2C12 mouse myoblasts reduces their ability to differentiate into myotubes as a result of premature cell cycle exit and early activation of the myogenic transcriptional program. This effect is rescued when cells are seeded at a high density or when cultured in conditioned medium from wild type cells. Proteomic analysis of collected medium indicates that SNAP23 depletion leads to a misregulation of exocytosis, including decreased secretion of the insulin-like growth factor 1 (IGF1), a critical protein for muscle growth, development, and function. We further demonstrate that treatment of SNAP23-depleted cells with exogenous IGF1 rescues their myogenic capacity. We propose that SNAP23 mediates the secretion of specific proteins, such as IGF1, that are important for achieving proper differentiation of skeletal muscle cells during myogenesis. This work highlights the underappreciated role of skeletal muscle as a secretory organ and contributes to the understanding of factors necessary for myogenesis.

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