4.6 Article

Activation of Sodium-Dependent Glutamate Transporters Regulates the Morphological Aspects of Oligodendrocyte Maturation via Signaling through Calcium/Calmodulin-Dependent Kinase IIβ's Actin-Binding/-Stabilizing Domain

Journal

GLIA
Volume 62, Issue 9, Pages 1543-1558

Publisher

WILEY
DOI: 10.1002/glia.22699

Keywords

myelin; calcium signaling; differentiation; central nervous system; actin cytoskeleton

Categories

Funding

  1. NIH-NINDS
  2. NIH [R01DA17310]
  3. Conacyt-Mexico
  4. Ministry of Education, Culture, Sports, Science, and Technology of Japan
  5. NIH-NINDS Center Core [5 P30 NS047463]
  6. Takeda Pharmaceuticals Co. Ltd.
  7. Fujitsu Laboratories
  8. Grants-in-Aid for Scientific Research [22110006, 26640020] Funding Source: KAKEN

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Signaling via the major excitatory amino acid glutamate has been implicated in the regulation of various aspects of the biology of oligodendrocytes, the myelinating cells of the central nervous system (CNS). In this respect, cells of the oligodendrocyte lineage have been described to express a variety of glutamate-responsive transmembrane proteins including sodium-dependent glutamate transporters. The latter have been well characterized to mediate glutamate clearance from the extracellular space. However, there is increasing evidence that they also mediate glutamate-induced intracellular signaling events. Our data presented here show that the activation of oligodendrocyte expressed sodium-dependent glutamate transporters, in particular GLT-1 and GLAST, promotes the morphological aspects of oligodendrocyte maturation. This effect was found to be associated with a transient increase in intracellular calcium levels and a transient phosphorylation event at the serine (S)(371) site of the calcium sensor calcium/calmodulin-dependent kinase type II beta (CaMKII beta). The potential regulatory S-371 site is located within CaMKII beta's previously defined actin-binding/-stabilizing domain, and phosphorylation events within this domain were identified in our studies as a requirement for sodium-dependent glutamate transporter-mediated promotion of oligodendrocyte maturation. Furthermore, our data provide good evidence for a role of these phosphorylation events in mediating detachment of CaMKII beta from filamentous (F)-actin, and hence allowing a remodeling of the oligodendrocyte's actin cytoskeleton. Taken together with our recent findings, which demonstrated a crucial role of CaMKII beta in regulating CNS myelination in vivo, our data strongly suggest that a sodium-dependent glutamate transporter-CaMKII beta-actin cytoskeleton axis plays an important role in the regulation of oligodendrocyte maturation and CNS myelination.

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