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Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration

Collective migration is important to embryonic development and cancer metastasis, but migratory and nonmigratory cell fate discrimination by differential activity of signal pathways remains elusive. In Drosophila oogenesis, Jak/Stat signaling patterns the epithelial cell fates in early egg chambers...

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Autores principales: Wu, Jhen-Wei, Wang, Chueh-Wen, Chen, Ruo-Yu, Hung, Liang-Yi, Tsai, Yu-Chen, Chan, Yu-Ting, Chang, Yu-Chiuan, Jang, Anna C.-C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307255/
https://www.ncbi.nlm.nih.gov/pubmed/35867785
http://dx.doi.org/10.1126/sciadv.abm2411
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author Wu, Jhen-Wei
Wang, Chueh-Wen
Chen, Ruo-Yu
Hung, Liang-Yi
Tsai, Yu-Chen
Chan, Yu-Ting
Chang, Yu-Chiuan
Jang, Anna C.-C.
author_facet Wu, Jhen-Wei
Wang, Chueh-Wen
Chen, Ruo-Yu
Hung, Liang-Yi
Tsai, Yu-Chen
Chan, Yu-Ting
Chang, Yu-Chiuan
Jang, Anna C.-C.
author_sort Wu, Jhen-Wei
collection PubMed
description Collective migration is important to embryonic development and cancer metastasis, but migratory and nonmigratory cell fate discrimination by differential activity of signal pathways remains elusive. In Drosophila oogenesis, Jak/Stat signaling patterns the epithelial cell fates in early egg chambers but later renders motility to clustered border cells. How Jak/Stat signal spatiotemporally switches static epithelia to motile cells is largely unknown. We report that a nuclear protein, Dysfusion, resides on the inner nuclear membrane and interacts with importin α/β and Nup153 to modulate Jak/Stat signal by attenuating Stat nuclear import. Dysfusion is ubiquitously expressed in oogenesis but specifically down-regulated in border cells when migrating. Increase of nuclear Stat by Dysfusion down-regulation triggers invasive cell behavior and maintains persistent motility. Mammalian homolog of Dysfusion (NPAS4) also negatively regulates the nuclear accumulation of STAT3 and cancer cell migration. Thus, our finding demonstrates that Dysfusion-dependent gating mechanism is conserved and may serve as a therapeutic target for Stat-mediated cancer metastasis.
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spelling pubmed-93072552022-08-09 Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration Wu, Jhen-Wei Wang, Chueh-Wen Chen, Ruo-Yu Hung, Liang-Yi Tsai, Yu-Chen Chan, Yu-Ting Chang, Yu-Chiuan Jang, Anna C.-C. Sci Adv Biomedicine and Life Sciences Collective migration is important to embryonic development and cancer metastasis, but migratory and nonmigratory cell fate discrimination by differential activity of signal pathways remains elusive. In Drosophila oogenesis, Jak/Stat signaling patterns the epithelial cell fates in early egg chambers but later renders motility to clustered border cells. How Jak/Stat signal spatiotemporally switches static epithelia to motile cells is largely unknown. We report that a nuclear protein, Dysfusion, resides on the inner nuclear membrane and interacts with importin α/β and Nup153 to modulate Jak/Stat signal by attenuating Stat nuclear import. Dysfusion is ubiquitously expressed in oogenesis but specifically down-regulated in border cells when migrating. Increase of nuclear Stat by Dysfusion down-regulation triggers invasive cell behavior and maintains persistent motility. Mammalian homolog of Dysfusion (NPAS4) also negatively regulates the nuclear accumulation of STAT3 and cancer cell migration. Thus, our finding demonstrates that Dysfusion-dependent gating mechanism is conserved and may serve as a therapeutic target for Stat-mediated cancer metastasis. American Association for the Advancement of Science 2022-07-22 /pmc/articles/PMC9307255/ /pubmed/35867785 http://dx.doi.org/10.1126/sciadv.abm2411 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Wu, Jhen-Wei
Wang, Chueh-Wen
Chen, Ruo-Yu
Hung, Liang-Yi
Tsai, Yu-Chen
Chan, Yu-Ting
Chang, Yu-Chiuan
Jang, Anna C.-C.
Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration
title Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration
title_full Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration
title_fullStr Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration
title_full_unstemmed Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration
title_short Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration
title_sort spatiotemporal gating of stat nuclear influx by drosophila npas4 in collective cell migration
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307255/
https://www.ncbi.nlm.nih.gov/pubmed/35867785
http://dx.doi.org/10.1126/sciadv.abm2411
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