The extracellular domain of teneurin-4 promotes cell adhesion for oligodendrocyte differentiation.

Biochem Biophys Res Commun

Department of Biochemistry and Biophysics, Graduate School of Health Care Sciences, TMDU, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8510, Japan; Department of Biochemistry and Biophysics, Graduate School of Medical and Dental Sciences, TMDU, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8510, Japan. Electronic address:

Published: February 2020

Cell adhesion between oligodendrocytes and neuronal axons is a critical step for myelination that enables the rapid propagation of action potential in the central nervous system. Here, we show that the transmembrane protein teneurin-4 plays a role in the cell adhesion required for the differentiation of oligodendrocytes. We found that teneurin-4 formed molecular complexes with all of the four teneurin family members and promoted cell-cell adhesion. Oligodendrocyte lineage cells attached to the recombinant extracellular domain of all the teneurins and formed well-branched cell processes. In an axon-mimicking nanofibers assay, nanofibers coated with the recombinant teneurin-4 extracellular domain increased the differentiation of oligodendrocytes. Our results show that teneurin-4 binds to all teneurins through their extracellular domain, which facilitates the oligodendrocyte-axon adhesion, and promotes oligodendrocyte differentiation via its homophilic interaction.

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http://dx.doi.org/10.1016/j.bbrc.2019.12.002DOI Listing

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