Oligodendroglial myelination requires astrocyte-derived lipids

Nutabi Camargo, Andrea Goudriaan, Anne Lieke F. van Deijk, Willem M. Otte, Jos F. Brouwers, Hans Lodder, David H. Gutmann, Klaus Armin Nave, Rick M. Dijkhuizen, Huibert D. Mansvelder, Roman Chrast, August B. Smit, Mark H.G. Verheijen

Research output: Contribution to journalArticlepeer-review

117 Scopus citations

Abstract

In the vertebrate nervous system, myelination of axons for rapid impulse propagation requires the synthesis of large amounts of lipids and proteins by oligodendrocytes and Schwann cells. Myelin membranes are thought to be cell-autonomously assembled by these axon-associated glial cells. Here, we report the surprising finding that in normal brain development, a substantial fraction of the lipids incorporated into central nervous system (CNS) myelin are contributed by astrocytes. The oligodendrocyte-specific inactivation of sterol regulatory element-binding protein (SREBP) cleavage-activating protein (SCAP), an essential coactivator of the transcription factor SREBP and thus of lipid biosynthesis, resulted in significantly retarded CNS myelination; however, myelin appeared normal at 3 months of age. Importantly, embryonic deletion of the same gene in astrocytes, or in astrocytes and oligodendrocytes, caused a persistent hypomyelination, as did deletion from astrocytes during postnatal development. Moreover, when astroglial lipid synthesis was inhibited, oligodendrocytes began incorporating circulating lipids into myelin membranes. Indeed, a lipid-enriched diet was sufficient to rescue hypomyelination in these conditional mouse mutants. We conclude that lipid synthesis by oligodendrocytes is heavily supplemented by astrocytes in vivo and that horizontal lipid flux is a major feature of normal brain development and myelination.

Original languageEnglish
Article numbere1002605
JournalPLoS biology
Volume15
Issue number5
DOIs
StatePublished - May 26 2017

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