Ablation of Dicer from murine Schwann cells increases their proliferation while blocking myelination

Juliane Bremer1, Tracy O'Connor, Cinzia Tiberi

  • 1Institute of Neuropathology, University Hospital of Zurich, Zurich, Switzerland.

Plos One
|September 1, 2010
PubMed

Insights

Regulatory microRNAs produced by Dicer1 are essential for peripheral nerve myelination. Ablating Dicer1 in Schwann cells halts differentiation, impairs myelination, and causes early death, highlighting microRNAs' critical role.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Genetics

Background:

  • Schwann cells produce myelin sheaths for peripheral nerve axons.
  • Schwann cell differentiation and myelination involve precise protein expression.
  • Regulatory mechanisms controlling these processes are not fully understood.

Purpose of the Study:

  • To investigate the role of Dicer1 and microRNAs in Schwann cell differentiation and myelination.
  • To identify microRNAs involved in peripheral nerve development.

Main Methods:

  • Schwann cell-specific ablation of Dicer1 in mice.
  • Analysis of Schwann cell differentiation, myelination, and cell death.
  • MicroRNA microarray analysis.

Main Results:

  • Dicer1 ablation in Schwann cells arrested differentiation and myelination, leading to postnatal lethality.
  • Dicer1-deficient Schwann cells could sort axons but not myelinate.
  • Cell death and immature Schwann cell proliferation increased, suggesting a role for microRNAs in growth arrest.
  • 16 microRNAs upregulated during myelination were identified and found to be Dicer-dependent.

Conclusions:

  • Dicer1-dependent microRNAs are crucial for Schwann cell differentiation and peripheral nerve myelination.
  • These microRNAs play a vital role in organismal survival by ensuring proper nerve development.

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