4.6 Article

Directional coupling of oligodendrocyte connexin-47 and astrocyte connexin-43 gap junctions

Journal

GLIA
Volume 66, Issue 11, Pages 2340-2352

Publisher

WILEY
DOI: 10.1002/glia.23471

Keywords

connexin-47; leukodystrophy; oligodendrocyte-astrocyte coupling; pore structure; rectification

Categories

Funding

  1. Spanish Government
  2. European Regional Development Fund [CSD2008_00005, BUF2012-33821, BUF2015-71078P, CTQ2009-10353]
  3. Community of Madrid [S2010/BMD-2460]

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Intercellular communication via gap junction channels between oligodendrocytes and between astrocytes as well as between these cell types is essential to maintain the integrity of myelin in the central nervous system. Oligodendrocyte gap junction connexin-47 (Cx47) is a key element in this crosstalk and indeed, mutations in human Cx47 cause severe myelin disorders. However, the permeation properties of channels of Cx47 alone and in heterotypic combination with astrocyte Cx43 remain unclear. We show here that Cx47 contains three extra residues at 5 ' amino-terminus that play a critical role in the channel pore structure and account for relative low ionic conductivity, cationic permselectivity and voltage-gating properties of oligodendrocyte-oligodendrocyte Cx47 channels. Regarding oligodendrocyte-astrocyte coupling, heterotypic channels formed by Cx47 with Cx43 exhibit ionic and chemical rectification, which creates a directional diffusion barrier for the movement of ions and larger negatively charged molecules from cells expressing Cx47 to those with Cx43. The restrictive permeability of Cx47 channels and the diffusion barrier of Cx47-Cx43 channels was abolished by a mutation associated with leukodystrophy, the Cx47P90S, suggesting a novel pathogenic mechanism underlying myelin disorders that involves alterations in the panglial permeation.

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