Publication

Galectin-4, a novel neuronal regulator of myelination

Stancic, M., Slijepcevic, D., Nomden, A., Vos, M. J., De Jonge, J. C., Sikkema, A. H., Gabius, H-J., Hoekstra, D. & Baron, W., May-2012, In : Glia. 60, 6, p. 919-935 17 p.

Research output: Contribution to journalArticleAcademicpeer-review

  • Mirjana Stancic
  • Davor Slijepcevic
  • Anita Nomden
  • Michel J. Vos
  • Jenny C. De Jonge
  • Arend H. Sikkema
  • Hans-J. Gabius
  • Dick Hoekstra
  • Wia Baron

Myelination of axons by oligodendrocytes (OLGs) is essential for proper saltatory nerve conduction, i.e., rapid transmission of nerve impulses. Among others, extracellular matrix (ECM) molecules, neuronal signaling, and axonal adhesion regulate the biogenesis and maintenance of myelin membranes, driven by polarized transport of myelin-specific proteins and lipids. Galectin-4, a tandem-repeat-type lectin with affinity to sulfatide and nonsialylated termini of N-glycans, has the ability to regulate adhesion of cells to ECM components and is also involved in polarized membrane trafficking. We, therefore, anticipated that galectin-4 might play a role in myelination. Here, we show that in developing postnatal rat brains galectin-4 expression is downregulated just before the onset of myelination. Intriguingly, when immature OLGs were treated with galectin-4, OLG maturation was retarded, while a subset of the immature OLGs reverted to a morphologically less complex progenitor stage, displaying concomitantly an increase in proliferation. Similarly, myelination was inhibited when galectin-4 or anti-galectin-4 antibodies were added to co-cultures of dorsal root ganglion neurons and OLGs. Neurons and OLGs were identified as a possible source of galectin-4, both in vitro and in vivo. In culture, neurons but not OLGs released galectin-4. Interestingly, in co-cultures, a reduced release of endogenous galectin-4 correlated with the onset of myelination. Moreover, galectin-4-reactive sites are transiently expressed on processes of premyelinating primary OLGs, but not on neurons. Taken together, these results identify neuronal galectin-4 as a candidate for a soluble regulator of OLG differentiation and, hence, myelination. (c) 2012 Wiley Periodicals, Inc.

Original languageEnglish
Pages (from-to)919-935
Number of pages17
JournalGlia
Volume60
Issue number6
Publication statusPublished - May-2012

    Keywords

  • development, galectin, myelination, neurons, oligodendrocytes, ENTEROCYTE-LIKE CELLS, PORCINE SMALL-INTESTINE, CENTRAL-NERVOUS-SYSTEM, OLIGODENDROCYTE DIFFERENTIATION, SCHWANN-CELLS, MONOCLONAL-ANTIBODY, MULTIPLE-SCLEROSIS, BINDING PROTEINS, IN-VITRO, EXPRESSION

ID: 5542251