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Phosphorylation sites of microtubule-associated protein 1B (MAP 1B) are involved in axon growth and regeneration

The growth cone is a specialized structure that forms at the tip of extending axons in developing and regenerating neurons. This structure is essential for accurate synaptogenesis at developmental stages, and is also involved in plasticity-dependent synaptogenesis and axon regeneration in the mature...

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Autores principales: Ishikawa, Yuya, Okada, Masayasu, Honda, Atsuko, Ito, Yasuyuki, Tamada, Atsushi, Endo, Naoto, Igarashi, Michihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849251/
https://www.ncbi.nlm.nih.gov/pubmed/31711525
http://dx.doi.org/10.1186/s13041-019-0510-z
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author Ishikawa, Yuya
Okada, Masayasu
Honda, Atsuko
Ito, Yasuyuki
Tamada, Atsushi
Endo, Naoto
Igarashi, Michihiro
author_facet Ishikawa, Yuya
Okada, Masayasu
Honda, Atsuko
Ito, Yasuyuki
Tamada, Atsushi
Endo, Naoto
Igarashi, Michihiro
author_sort Ishikawa, Yuya
collection PubMed
description The growth cone is a specialized structure that forms at the tip of extending axons in developing and regenerating neurons. This structure is essential for accurate synaptogenesis at developmental stages, and is also involved in plasticity-dependent synaptogenesis and axon regeneration in the mature brain. Thus, understanding the molecular mechanisms utilized by growth cones is indispensable to understanding neuronal network formation and rearrangement. Phosphorylation is the most important and commonly utilized protein modification in signal transduction. We previously identified microtubule-associated protein 1B (MAP 1B) as the most frequently phosphorylated protein among ~ 1200 phosphorylated proteins. MAP 1B has more than 10 phosphorylation sites that were present more than 50 times among these 1200 proteins. Here, we produced phospho-specific antibodies against phosphorylated serines at positions 25 and 1201 of MAP 1B that specifically recognize growing axons both in cultured neurons and in vivo in various regions of the embryonic brain. Following sciatic nerve injury, immunoreactivity with each antibody increased compared to the sham operated group. Experiments with transected and sutured nerves revealed that regenerating axons were specifically recognized by these antibodies. These results suggest that these MAP 1B phosphorylation sites are specifically involved in axon growth and that phospho-specific antibodies against MAP 1B are useful markers of growing/regenerating axons.
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spelling pubmed-68492512019-11-15 Phosphorylation sites of microtubule-associated protein 1B (MAP 1B) are involved in axon growth and regeneration Ishikawa, Yuya Okada, Masayasu Honda, Atsuko Ito, Yasuyuki Tamada, Atsushi Endo, Naoto Igarashi, Michihiro Mol Brain Research The growth cone is a specialized structure that forms at the tip of extending axons in developing and regenerating neurons. This structure is essential for accurate synaptogenesis at developmental stages, and is also involved in plasticity-dependent synaptogenesis and axon regeneration in the mature brain. Thus, understanding the molecular mechanisms utilized by growth cones is indispensable to understanding neuronal network formation and rearrangement. Phosphorylation is the most important and commonly utilized protein modification in signal transduction. We previously identified microtubule-associated protein 1B (MAP 1B) as the most frequently phosphorylated protein among ~ 1200 phosphorylated proteins. MAP 1B has more than 10 phosphorylation sites that were present more than 50 times among these 1200 proteins. Here, we produced phospho-specific antibodies against phosphorylated serines at positions 25 and 1201 of MAP 1B that specifically recognize growing axons both in cultured neurons and in vivo in various regions of the embryonic brain. Following sciatic nerve injury, immunoreactivity with each antibody increased compared to the sham operated group. Experiments with transected and sutured nerves revealed that regenerating axons were specifically recognized by these antibodies. These results suggest that these MAP 1B phosphorylation sites are specifically involved in axon growth and that phospho-specific antibodies against MAP 1B are useful markers of growing/regenerating axons. BioMed Central 2019-11-11 /pmc/articles/PMC6849251/ /pubmed/31711525 http://dx.doi.org/10.1186/s13041-019-0510-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ishikawa, Yuya
Okada, Masayasu
Honda, Atsuko
Ito, Yasuyuki
Tamada, Atsushi
Endo, Naoto
Igarashi, Michihiro
Phosphorylation sites of microtubule-associated protein 1B (MAP 1B) are involved in axon growth and regeneration
title Phosphorylation sites of microtubule-associated protein 1B (MAP 1B) are involved in axon growth and regeneration
title_full Phosphorylation sites of microtubule-associated protein 1B (MAP 1B) are involved in axon growth and regeneration
title_fullStr Phosphorylation sites of microtubule-associated protein 1B (MAP 1B) are involved in axon growth and regeneration
title_full_unstemmed Phosphorylation sites of microtubule-associated protein 1B (MAP 1B) are involved in axon growth and regeneration
title_short Phosphorylation sites of microtubule-associated protein 1B (MAP 1B) are involved in axon growth and regeneration
title_sort phosphorylation sites of microtubule-associated protein 1b (map 1b) are involved in axon growth and regeneration
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849251/
https://www.ncbi.nlm.nih.gov/pubmed/31711525
http://dx.doi.org/10.1186/s13041-019-0510-z
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