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.
Highlights
Proper myelination is essential for the efficient saltatory conduction of action potentials, the trophic support of axons, and the maintenance of axonal integrity in the peripheral nervous system (PNS)
The mature myelin sheaths wrapped around the large-diameter axons of peripheral neurons arise from neural crest cells which subsequently develop into Schwann cell precursors (SCPs), immature Schwann cells, and mature myelinating or nonmyelinating Schwann cells
The Cre recombinase in these mice is already active in Schwann cells of the precursor stage at embryonic day 12/13 (E12/13) [15]
Summary
Proper myelination is essential for the efficient saltatory conduction of action potentials, the trophic support of axons, and the maintenance of axonal integrity in the peripheral nervous system (PNS). Defective PNS myelination occurs in hereditary peripheral neuropathies [1]. Each stage of Schwann cell development is associated with a set of specific protein markers, the expression of which is thought to be driven primarily by axonderived signals at the SCP stage and by the secretion of autocrine survival factors at the Schwann cell stage (reviewed in [3]). This precise developmental program requires tightly regulated transcriptional and post-transcriptional control of protein expression, the details of which are still incompletely understood
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