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Collapsin response mediator protein‐2 phosphorylation promotes the reversible retraction of oligodendrocyte processes in response to non‐lethal oxidative stress
Author(s) -
FernándezGamba Agata,
Leal María Celeste,
Maarouf Chera L.,
RichterLandsberg Christiane,
Wu Terence,
Morelli Laura,
Roher Alex E.,
Castaño Eduardo M.
Publication year - 2012
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2012.07742.x
Subject(s) - mediator , oxidative stress , phosphorylation , fight or flight response , oxidative phosphorylation , oligodendrocyte , microbiology and biotechnology , chemistry , neuroscience , biology , biophysics , biochemistry , myelin , central nervous system , gene
J. Neurochem. (2012) 121 , 985–995. Abstract The extension of processes of oligodendrocyte (OLG) and their precursor cells are crucial for migration, axonal contact and myelination. Here we show that a non‐lethal oxidative stress induced by 3‐nitropropionic acid (3‐NP) elicited a rapid shortening of processes (∼24%) in primary OLGs and in oligodendroglial cell line (OLN‐93) cells (∼36%) as compared with vehicle‐exposed cells. This was reversible and prevented by antioxidants. Proteomics of OLG lysates with and without 3‐NP treatment yielded collapsin response mediator protein 2 (CRMP‐2) as a candidate effector molecule. Inhibition of rho kinase was sufficient to prevent process retraction in both OLGs and OLN‐93 cells. Oxidative stress increased phosphorylation of CRMP‐2 at T555 that was completely prevented by Y27632. Moreover, transfection of OLN‐93 cells with the mutant CRMP‐2 T555A which cannot be phosphorylated by rho kinase, prevented process shortening induced by 3‐NP as compared with wild‐type CRMP‐2. Our results suggest a role for endogenous reactive oxygen species in a pathway that regulates OLG process extension. The vulnerability of late myelinated neurons in the adult brain and the presence of white matter pathology in human dementias warrant the study of this oligodendroglial pathway in the early stages of neurodegenerative conditions characterized by oxidative stress.