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Analyzing Murine Schwann Cell Development Along Growing Axons
Published on: November 21, 2012
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.
Abstract:
The myelin sheaths that surround the thick axons of the peripheral nervous system are produced by the highly specialized Schwann cells. Differentiation of Schwann cells and myelination occur in discrete steps. Each of these requires coordinated expression of specific proteins in a precise sequence, yet the regulatory mechanisms controlling protein expression during these events are incompletely understood. Here we report that Schwann cell-specific ablation of the enzyme Dicer1, which is required for the production of small non-coding regulatory microRNAs, fully arrests Schwann cell differentiation, resulting in early postnatal lethality. Dicer(-/-) Schwann cells had lost their ability to myelinate, yet were still capable of sorting axons. Both cell death and, paradoxically, proliferation of immature Schwann cells was markedly enhanced, suggesting that their terminal differentiation is triggered by growth-arresting regulatory microRNAs. Using microRNA microarrays, we identified 16 microRNAs that are upregulated upon myelination and whose expression is controlled by Dicer in Schwann cells. This set of microRNAs appears to drive Schwann cell differentiation and myelination of peripheral nerves, thereby fulfilling a crucial function for survival of the organism.
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.
