55
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      c-Jun Reprograms Schwann Cells of Injured Nerves to Generate a Repair Cell Essential for Regeneration

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          The radical response of peripheral nerves to injury (Wallerian degeneration) is the cornerstone of nerve repair. We show that activation of the transcription factor c-Jun in Schwann cells is a global regulator of Wallerian degeneration. c-Jun governs major aspects of the injury response, determines the expression of trophic factors, adhesion molecules, the formation of regeneration tracks and myelin clearance and controls the distinctive regenerative potential of peripheral nerves. A key function of c-Jun is the activation of a repair program in Schwann cells and the creation of a cell specialized to support regeneration. We show that absence of c-Jun results in the formation of a dysfunctional repair cell, striking failure of functional recovery, and neuronal death. We conclude that a single glial transcription factor is essential for restoration of damaged nerves, acting to control the transdifferentiation of myelin and Remak Schwann cells to dedicated repair cells in damaged tissue.

          Highlights

          ► Schwann cell c-Jun is a master regulator of the PNS injury response ► c-Jun activates a defined repair program in Schwann cells of damaged nerves ► c-Jun controls transdifferentiation of differentiated Schwann cells to repair cells ► Schwann cell c-Jun is essential for neuronal survival and functional recovery

          Abstract

          Unlike the central nervous system, injured peripheral nerves regenerate to restore function after injury. Arthur-Farraj et al. show that this repair potential depends on glial (Schwann) cell expression of the transcription factor c-Jun.

          Related collections

          Most cited references17

          • Record: found
          • Abstract: found
          • Article: not found

          The origin and development of glial cells in peripheral nerves.

          During the development of peripheral nerves, neural crest cells generate myelinating and non-myelinating glial cells in a process that parallels gliogenesis from the germinal layers of the CNS. Unlike central gliogenesis, neural crest development involves a protracted embryonic phase devoted to the generation of, first, the Schwann cell precursor and then the immature Schwann cell, a cell whose fate as a myelinating or non-myelinating cell has yet to be determined. Embryonic nerves therefore offer a particular opportunity to analyse the early steps of gliogenesis from transient multipotent stem cells, and to understand how this process is integrated with organogenesis of peripheral nerves.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Wallerian degeneration, wld(s), and nmnat.

            Traditionally, researchers have believed that axons are highly dependent on their cell bodies for long-term survival. However, recent studies point to the existence of axon-autonomous mechanism(s) that regulate rapid axon degeneration after axotomy. Here, we review the cellular and molecular events that underlie this process, termed Wallerian degeneration. We describe the biphasic nature of axon degeneration after axotomy and our current understanding of how Wld(S)--an extraordinary protein formed by fusing a Ube4b sequence to Nmnat1--acts to protect severed axons. Interestingly, the neuroprotective effects of Wld(S) span all species tested, which suggests that there is an ancient, Wld(S)-sensitive axon destruction program. Recent studies with Wld(S) also reveal that Wallerian degeneration is genetically related to several dying back axonopathies, thus arguing that Wallerian degeneration can serve as a useful model to understand, and potentially treat, axon degeneration in diverse traumatic or disease contexts.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Extreme makeover: converting one cell into another.

              Cells of adult mammals can be converted (reprogrammed) to new cells. In one approach, adult cells are converted to pluripotent stem cells, followed by differentiation to regenerate new cell types. Alternatively, adult cells may be directly converted into other mature cells or progenitors. We discuss and compare these two approaches with particular emphasis on the latter and its relevance for regenerative medicine.
                Bookmark

                Author and article information

                Journal
                Neuron
                Neuron
                Neuron
                Cell Press
                0896-6273
                1097-4199
                23 August 2012
                23 August 2012
                : 75
                : 4
                : 633-647
                Affiliations
                [1 ]Department of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK
                [2 ]Metabolomics Unit, CICbioGune, Parque Tecnológico de Bizcaia, 48160 Derio, Bizcaia, Spain
                [3 ]Neuro-Oncology Group, Department of Immunology, Genetics and Pathology, Uppsala University, Dag Hammarskjölds väg 20, 751 85 Uppsala, Sweden
                [4 ]Sobell Department of Motor Neuroscience & Movement Disorders, University College London Institute of Neurology, Queen Square House, London WC1N 3BG, UK
                [5 ]Mammalian Genetics Laboratory, London Research Institute, CRUK, 44 Lincoln’s Inn Fields, London WC2A 3LY, UK
                [6 ]Perinatal Brain Group, Department of Obstetrics and Gynaecology and Department of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK
                Author notes
                []Corresponding author k.jessen@ 123456ucl.ac.uk
                [7]

                These authors contributed equally to this work

                Article
                NEURON11200
                10.1016/j.neuron.2012.06.021
                3657176
                22920255
                b3c209d4-a0da-41a0-8dd7-51d11602197c
                © 2012 ELL & Excerpta Medica.

                This document may be redistributed and reused, subject to certain conditions.

                History
                : 4 June 2012
                Categories
                Article

                Neurosciences
                Neurosciences

                Comments

                Comment on this article