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Axon Regeneration Requires a Conserved MAP Kinase Pathway
Author(s) -
Marc Hammarlund,
Paola Nix,
Linda Hauth,
Erik M. Jørgensen,
Michael J. Bastiani
Publication year - 2009
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1165527
Subject(s) - regeneration (biology) , axon , biology , microbiology and biotechnology , growth cone , caenorhabditis elegans , mitogen activated protein kinase , neuroscience , kinase , signal transduction , protein kinase a , genetics , gene
Regeneration of injured neurons can restore function, but most neurons regenerate poorly or not at all. The failure to regenerate in some cases is due to a lack of activation of cell-intrinsic regeneration pathways. These pathways might be targeted for the development of therapies that can restore neuron function after injury or disease. Here, we show that the DLK-1 mitogen-activated protein (MAP) kinase pathway is essential for regeneration in Caenorhabditis elegans motor neurons. Loss of this pathway eliminates regeneration, whereas activating it improves regeneration. Further, these proteins also regulate the later step of growth cone migration. We conclude that after axon injury, activation of this MAP kinase cascade is required to switch the mature neuron from an aplastic state to a state capable of growth.

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