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Cdk5-mediated JIP1 phosphorylation regulates axonal outgrowth through Notch1 inhibition

BACKGROUND: Activated Cdk5 regulates a number of processes during nervous system formation, including neuronal differentiation, growth cone stabilization, and axonal growth. Cdk5 phosphorylates its downstream substrates located in axonal growth cones, where the highly expressed c-Jun N-terminal kina...

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Autores principales: Im, Doo Soon, Joselin, Alvin, Svoboda, Devon, Takano, Tesuya, Rousseaux, Maxime W. C., Callaghan, Steve, Slack, Ruth S., Hisanaga, Shin-ichi, Davis, Roger J., Park, David S., Qu, Dianbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115922/
https://www.ncbi.nlm.nih.gov/pubmed/35581583
http://dx.doi.org/10.1186/s12915-022-01312-4
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author Im, Doo Soon
Joselin, Alvin
Svoboda, Devon
Takano, Tesuya
Rousseaux, Maxime W. C.
Callaghan, Steve
Slack, Ruth S.
Hisanaga, Shin-ichi
Davis, Roger J.
Park, David S.
Qu, Dianbo
author_facet Im, Doo Soon
Joselin, Alvin
Svoboda, Devon
Takano, Tesuya
Rousseaux, Maxime W. C.
Callaghan, Steve
Slack, Ruth S.
Hisanaga, Shin-ichi
Davis, Roger J.
Park, David S.
Qu, Dianbo
author_sort Im, Doo Soon
collection PubMed
description BACKGROUND: Activated Cdk5 regulates a number of processes during nervous system formation, including neuronal differentiation, growth cone stabilization, and axonal growth. Cdk5 phosphorylates its downstream substrates located in axonal growth cones, where the highly expressed c-Jun N-terminal kinase (JNK)-interacting protein1 (JIP1) has been implicated as another important regulator of axonal growth. In addition, stringent control of the level of intracellular domain of Notch1 (Notch1-IC) plays a regulatory role in axonal outgrowth during neuronal differentiation. However, whether Cdk5-JIP1-Notch1 cooperate to regulate axonal outgrowth, and the mechanism of such joint contribution to this pathway, is presently unknown, and here we explore their potential interaction. RESULTS: Our interactome screen identified JIP1 as an interactor of p35, a Cdk5 activator, and we sought to explore the relationship between Cdk5 and JIP1 on the regulation of axonal outgrowth. We demonstrate that JIP1 phosphorylated by Cdk5 at Thr205 enhances axonal outgrowth and a phosphomimic JIP1 rescues the axonal outgrowth defects in JIP1(−/−) and p35(−/−) neurons. Axonal outgrowth defects caused by the specific increase of Notch1 in JIP1(−/−) neurons are rescued by Numb-mediated inhibition of Notch1. Finally, we demonstrate that Cdk5 phosphorylation of JIP1 further amplifies the phosphorylation status of yet another Cdk5 substrate E3-ubiquitin ligase Itch, resulting in increased Notch1 ubiquitination. CONCLUSIONS: Our findings identify a potentially critical signaling axis involving Cdk5-JIP1-Itch-Notch1, which plays an important role in the regulation of CNS development. Future investigation into the way this pathway integrates with additional pathways regulating axonal growth will further our knowledge of normal central nervous system development and pathological conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01312-4.
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spelling pubmed-91159222022-05-19 Cdk5-mediated JIP1 phosphorylation regulates axonal outgrowth through Notch1 inhibition Im, Doo Soon Joselin, Alvin Svoboda, Devon Takano, Tesuya Rousseaux, Maxime W. C. Callaghan, Steve Slack, Ruth S. Hisanaga, Shin-ichi Davis, Roger J. Park, David S. Qu, Dianbo BMC Biol Research Article BACKGROUND: Activated Cdk5 regulates a number of processes during nervous system formation, including neuronal differentiation, growth cone stabilization, and axonal growth. Cdk5 phosphorylates its downstream substrates located in axonal growth cones, where the highly expressed c-Jun N-terminal kinase (JNK)-interacting protein1 (JIP1) has been implicated as another important regulator of axonal growth. In addition, stringent control of the level of intracellular domain of Notch1 (Notch1-IC) plays a regulatory role in axonal outgrowth during neuronal differentiation. However, whether Cdk5-JIP1-Notch1 cooperate to regulate axonal outgrowth, and the mechanism of such joint contribution to this pathway, is presently unknown, and here we explore their potential interaction. RESULTS: Our interactome screen identified JIP1 as an interactor of p35, a Cdk5 activator, and we sought to explore the relationship between Cdk5 and JIP1 on the regulation of axonal outgrowth. We demonstrate that JIP1 phosphorylated by Cdk5 at Thr205 enhances axonal outgrowth and a phosphomimic JIP1 rescues the axonal outgrowth defects in JIP1(−/−) and p35(−/−) neurons. Axonal outgrowth defects caused by the specific increase of Notch1 in JIP1(−/−) neurons are rescued by Numb-mediated inhibition of Notch1. Finally, we demonstrate that Cdk5 phosphorylation of JIP1 further amplifies the phosphorylation status of yet another Cdk5 substrate E3-ubiquitin ligase Itch, resulting in increased Notch1 ubiquitination. CONCLUSIONS: Our findings identify a potentially critical signaling axis involving Cdk5-JIP1-Itch-Notch1, which plays an important role in the regulation of CNS development. Future investigation into the way this pathway integrates with additional pathways regulating axonal growth will further our knowledge of normal central nervous system development and pathological conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01312-4. BioMed Central 2022-05-17 /pmc/articles/PMC9115922/ /pubmed/35581583 http://dx.doi.org/10.1186/s12915-022-01312-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Im, Doo Soon
Joselin, Alvin
Svoboda, Devon
Takano, Tesuya
Rousseaux, Maxime W. C.
Callaghan, Steve
Slack, Ruth S.
Hisanaga, Shin-ichi
Davis, Roger J.
Park, David S.
Qu, Dianbo
Cdk5-mediated JIP1 phosphorylation regulates axonal outgrowth through Notch1 inhibition
title Cdk5-mediated JIP1 phosphorylation regulates axonal outgrowth through Notch1 inhibition
title_full Cdk5-mediated JIP1 phosphorylation regulates axonal outgrowth through Notch1 inhibition
title_fullStr Cdk5-mediated JIP1 phosphorylation regulates axonal outgrowth through Notch1 inhibition
title_full_unstemmed Cdk5-mediated JIP1 phosphorylation regulates axonal outgrowth through Notch1 inhibition
title_short Cdk5-mediated JIP1 phosphorylation regulates axonal outgrowth through Notch1 inhibition
title_sort cdk5-mediated jip1 phosphorylation regulates axonal outgrowth through notch1 inhibition
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115922/
https://www.ncbi.nlm.nih.gov/pubmed/35581583
http://dx.doi.org/10.1186/s12915-022-01312-4
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