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February 22, 2026Journal of Neurochemistry0 citationsOpen Access

Glia‐to‐Axon Transfer of Ribosomes and miRNAs : A Novel Paradigm in Neural Repair

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FMFrancisca Marín‐VenegasFCFelipe A. Court

Key Points

  • To examine the role of Schwann cell-derived exosomes in promoting nerve repair through ribosome transfer and miRNA delivery.
  • Investigated intercellular communication via Schwann cell-derived exosomes
  • Analyzed effects on axon regrowth and remyelination in various models
  • Studied the cargo delivered by exosomes, including miRNAs, mRNAs, and proteins
  • Schwann cell-derived exosomes enhance axon regrowth and remyelination outcomes
  • Demonstrated improved functional recovery across multiple models
  • Identified specific cargo that modulates neuronal and glial response

Abstract

ABSTRACT Schwann cells communicate with neurons not only through soluble cues but also via intercellular transfer of ribosomes and exosome‐mediated delivery of cargo. Recent studies have established that Schwann cell‐derived exosomes are powerful promoters of nerve repair, capable of enhancing axon regrowth, remyelination, and functional recovery in numerous models. These effects are mediated via multifactorial cargo (miRNAs, mRNAs, proteins) that modulate neurons, glia, endothelial, and immune cells. Importantly, what began as a novel biological insight is now rapidly moving toward therapeutic innovation. Schwann cell‐derived exosomes thus represent both a novel mode of glia–neuron communication and a promising avenue for next‐generation therapies for nerve regeneration. image

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Cite This Study

Marín‐Venegas et al. (2026) studied this question.

synapsesocial.com/papers/699a9d65482488d673cd3378https://doi.org/10.1111/jnc.70386
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