4.7 Article

GPR56/ADGRG1 regulates development and maintenance of peripheral myelin

Journal

JOURNAL OF EXPERIMENTAL MEDICINE
Volume 215, Issue 3, Pages 941-961

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20161714

Keywords

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Funding

  1. National Institutes of Health [F31 NS087801, F31 NS094004, F32 NS100461, R01NS045630, K23 NS084932, R01 NS079445]
  2. Muscular Dystrophy Association [293295]
  3. Edward J. Mallinckrodt, Jr. Foundation
  4. European Research Council
  5. Swiss National Science Foundation
  6. Clinical Research Priority Programs Small RNAs and Human Hemato-Lymphatic Diseases, SystemsX.ch (PrionX)
  7. Novartis Foundation
  8. Synapsis Foundation
  9. Clinical Research Priority Programs Small RNAs and Human Hemato-Lymphatic Diseases, SystemsX.ch (SynucleiX)
  10. European Union Seventh Framework Programme grant (NEURINOX)
  11. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [R21HD075363] Funding Source: NIH RePORTER
  12. NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES [UL1TR001412] Funding Source: NIH RePORTER
  13. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [F31NS087801, K23NS084932, F31NS094004, R01NS094164, R01NS045630, F32NS100461, R01NS079445] Funding Source: NIH RePORTER

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Myelin is a multilamellar sheath generated by specialized glia called Schwann cells (SCs) in the peripheral nervous system (PNS), which serves to protect and insulate axons for rapid neuronal signaling. In zebrafish and rodent models, we identify GPR56/ADGRG1 as a conserved regulator of PNS development and health. We demonstrate that, during SC development, GPR56-dependent RhoA signaling promotes timely radial sorting of axons. In the mature PNS, GPR56 is localized to distinct SC cytoplasmic domains, is required to establish proper myelin thickness, and facilitates organization of the myelin sheath. Furthermore, we define plectin-a scaffolding protein previously linked to SC domain organization, myelin maintenance, and a series of disorders termed plectinopathies-as a novel interacting partner of GPR56. Finally, we show that Gpr56 mutants develop progressive neuropathy-like symptoms, suggesting an underlying mechanism for peripheral defects in some human patients with GPR56 mutations. In sum, we define Gpr56 as a new regulator in the development and maintenance of peripheral myelin.

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