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CRMP4-mediated fornix development involves Semaphorin-3E signaling pathway

Тип публикацииJournal Article
Дата публикации2021-12-03
SCImago Q1
Tоп 10% SCImago
БС1
SJR3.395
CiteScore12.9
Impact factor6.4
ISSN2050084X
General Biochemistry, Genetics and Molecular Biology
General Medicine
General Immunology and Microbiology
General Neuroscience
Краткое описание

Neurodevelopmental axonal pathfinding plays a central role in correct brain wiring and subsequent cognitive abilities. Within the growth cone, various intracellular effectors transduce axonal guidance signals by remodeling the cytoskeleton. Semaphorin-3E (Sema3E) is a guidance cue implicated in development of the fornix, a neuronal tract connecting the hippocampus to the hypothalamus. Microtubule-associated protein 6 (MAP6) has been shown to be involved in the Sema3E growth-promoting signaling pathway. In this study, we identified the collapsin response mediator protein 4 (CRMP4) as a MAP6 partner and a crucial effector in Sema3E growth-promoting activity. CRMP4-KO mice displayed abnormal fornix development reminiscent of that observed in Sema3E-KO mice. CRMP4 was shown to interact with the Sema3E tripartite receptor complex within detergent-resistant membrane (DRM) domains, and DRM domain integrity was required to transduce Sema3E signaling through the Akt/GSK3 pathway. Finally, we showed that the cytoskeleton-binding domain of CRMP4 is required for Sema3E’s growth-promoting activity, suggesting that CRMP4 plays a role at the interface between Sema3E receptors, located in DRM domains, and the cytoskeleton network. As the fornix is affected in many psychiatric diseases, such as schizophrenia, our results provide new insights to better understand the neurodevelopmental components of these diseases.

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Seminars in Cell and Developmental Biology
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Neurobiology of Disease
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Frontiers in Cellular Neuroscience
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ГОСТ |
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Boulan B. et al. CRMP4-mediated fornix development involves Semaphorin-3E signaling pathway // eLife. 2021. Vol. 10.
ГОСТ со всеми авторами (до 50) Скопировать
Boulan B., Ravanello C., Peyrel A., Bosc C., Delphin C., Appaix F., Denarier E., Kraut A., Jacquier-Sarlin M., Fournier A., Andrieux A., Gory Fauré S., Deloulme J. CRMP4-mediated fornix development involves Semaphorin-3E signaling pathway // eLife. 2021. Vol. 10.
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TY - JOUR
DO - 10.7554/elife.70361
UR - https://doi.org/10.7554/elife.70361
TI - CRMP4-mediated fornix development involves Semaphorin-3E signaling pathway
T2 - eLife
AU - Boulan, Benoit
AU - Ravanello, Charlotte
AU - Peyrel, Amandine
AU - Bosc, Christophe
AU - Delphin, Christian
AU - Appaix, Florence
AU - Denarier, E.
AU - Kraut, Alexandra
AU - Jacquier-Sarlin, Muriel
AU - Fournier, Alyson
AU - Andrieux, Annie
AU - Gory Fauré, Sylvie
AU - Deloulme, JC
PY - 2021
DA - 2021/12/03
PB - eLife Sciences Publications
VL - 10
PMID - 34860155
SN - 2050-084X
ER -
BibTex
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BibTex (до 50 авторов) Скопировать
@article{2021_Boulan,
author = {Benoit Boulan and Charlotte Ravanello and Amandine Peyrel and Christophe Bosc and Christian Delphin and Florence Appaix and E. Denarier and Alexandra Kraut and Muriel Jacquier-Sarlin and Alyson Fournier and Annie Andrieux and Sylvie Gory Fauré and JC Deloulme},
title = {CRMP4-mediated fornix development involves Semaphorin-3E signaling pathway},
journal = {eLife},
year = {2021},
volume = {10},
publisher = {eLife Sciences Publications},
month = {dec},
url = {https://doi.org/10.7554/elife.70361},
doi = {10.7554/elife.70361}
}
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