Process outgrowth in oligodendrocytes is mediated by CNP, a novel microtubule assembly myelin protein

Author:

Lee John1,Gravel Michel1,Zhang Rulin2,Thibault Pierre3,Braun Peter E.1

Affiliation:

1. Department of Biochemistry, McGill University, Montreal, Quebec H3G 1Y6, Canada

2. WEMB Biochem, Inc., Toronto, Ontario M9W 1E7, Canada

3. Institut de Recherches en Immunologie et Cancer, Université de Montréal, Montreal, Quebec H3C 3J7, Canada

Abstract

Oligodendrocytes (OLs) extend arborized processes that are supported by microtubules (MTs) and microfilaments. Little is known about proteins that modulate and interact with the cytoskeleton during myelination. Several lines of evidence suggest a role for 2′,3′-cyclic nucleotide 3′-phosphodiesterase (CNP) in mediating process formation in OLs. In this study, we report that tubulin is a major CNP-interacting protein. In vitro, CNP binds preferentially to tubulin heterodimers compared with MTs and induces MT assembly by copolymerizing with tubulin. CNP overexpression induces dramatic morphology changes in both glial and nonglial cells, resulting in MT and F-actin reorganization and formation of branched processes. These morphological effects are attributed to CNP MT assembly activity; branched process formation is either substantially reduced or abolished with the expression of loss-of-function mutants. Accordingly, cultured OLs from CNP-deficient mice extend smaller outgrowths with less arborized processes. We propose that CNP is an important component of the cytoskeletal machinery that directs process outgrowth in OLs.

Publisher

Rockefeller University Press

Subject

Cell Biology

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