9.9
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Volume 51 Issue 9
Sep.  2024
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Article Navigation >  Journal of Genetics and Genomics  > 2024  >  51(9): 911-921

microRNA-2184 orchestrates Mauthner-cell axon regeneration in zebrafish via syt3 modulation

doi: 10.1016/j.jgg.2024.03.016
  •  

    a. Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui 230026, China;

  •  

    b. The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230026, China;

  •  

    c. Center for Advanced Interdisciplinary Science and Biomedicine of IHM, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230026, China

Funds:

This work was supported by the Research Funds of the Center for Advanced Interdisciplinary Science and Biomedicine of IHM (QYZD20220002), the National Natural Science Foundation of China (82071357), and the Ministry of Science and Technology of China (2019YFA0405600 to B.H.).

  • Received Date: 2024-03-26
  • Accepted Date: 2024-03-30
  • Rev Recd Date: 2024-03-30
    • Available Online: 2025-06-06
  • Publish Date: 2024-04-04
    Abstract
  • MicroRNAs (miRNAs) play a significant role in axon regeneration following spinal cord injury. However, the functions of numerous miRNAs in axon regeneration within the central nervous system (CNS) remain largely unexplored. Here, we elucidate the positive role of microRNA-2184 (miR-2184) in axon regeneration within zebrafish Mauthner cells (M-cells). The upregulation of miR-2184 in a single M-cell can facilitate axon regeneration, while the specific sponge-induced silencing of miR-2184 leads to impeded regeneration. We show that syt3, a downstream target of miR-2184, negatively regulates axon regeneration, and the regeneration suppression modulated by syt3 depends on its binding to Ca2+. Furthermore, pharmacological stimulation of the cAMP/PKA pathway suggests that changes in the readily releasable pool may affect axon regeneration. Our data indicate that miR-2184 promotes axon regeneration of M-cells within the CNS by modulating the downstream target syt3, providing valuable insights into potential therapeutic strategies.
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