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Peripheral nervous system plasmalogens regulate Schwann cell differentiation and myelination

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  • معلومة اضافية
    • Contributors:
      Instituto de Investigação e Inovação em Saúde
    • بيانات النشر:
      American Society for Clinical Investigation
    • الموضوع:
      2014
    • Collection:
      Repositório Aberto da Universidade do Porto
    • نبذة مختصرة :
      Rhizomelic chondrodysplasia punctata (RCDP) is a developmental disorder characterized by hypotonia, cataracts, abnormal ossification, impaired motor development, and intellectual disability. The underlying etiology of RCDP is a deficiency in the biosynthesis of ether phospholipids, of which plasmalogens are the most abundant form in nervous tissue and myelin; however, the role of plasmalogens in the peripheral nervous system is poorly defined. Here, we used mouse models of RCDP and analyzed the consequence of plasmalogen deficiency in peripheral nerves. We determined that plasmalogens are crucial for Schwann cell development and differentiation and that plasmalogen defects impaired radial sorting, myelination, and myelin structure. Plasmalogen insufficiency resulted in defective protein kinase B (AKT) phosphorylation and subsequent signaling, causing overt activation of glycogen synthase kinase 3β (GSK3β) in nerves of mutant mice. Treatment with GSK3β inhibitors, lithium, or 4-benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione (TDZD-8) restored Schwann cell defects, effectively bypassing plasmalogen deficiency. Our results demonstrate the requirement of plasmalogens for the correct and timely differentiation of Schwann cells and for the process of myelination. In addition, these studies identify a mechanism by which the lack of a membrane phospholipid causes neuropathology, implicating plasmalogens as regulators of membrane and cell signaling. ; We thank Paula Sampaio for microscopy support, Paula Magalhdes for genotyping, and Isabel Carvalho, Sofia Lamas, and Fatima Martins for excellent animal care. We are grateful to P. Brophy (University of Edinburgh) for the DRP2 antibody and to M. Baes (K.U. Leuven) for providing the Gnpat mouse strain. This work was funded by the Research Foundation of the European Leukodystrophy Association (ELA 2008-009C4, ELA 2010-042C5), by FEDER Funds through the Operational Competitiveness Program - COMPETE, and by national funds through the FCT - Fundacao para a Ciencia e a Tecnologia ...
    • File Description:
      application/pdf
    • ISSN:
      0021-9738
    • Relation:
      info:eu-repo/grantAgreement/FCT/5876-PPCDTI/112406/PT; info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F88160%2F2012/PT; The Journal of Clinical Investigation, vol. 124(6), p. 2560-70; https://www.jci.org/articles/view/72063; http://hdl.handle.net/10216/110350
    • الرقم المعرف:
      10.1172/JCI72063
    • الدخول الالكتروني :
      http://hdl.handle.net/10216/110350
      https://doi.org/10.1172/JCI72063
    • Rights:
      info:eu-repo/semantics/openAccess
    • الرقم المعرف:
      edsbas.A58C3323