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Mechanosensitive accumulation of non-muscle myosin IIB during mitosis requires its translocation activity
Non-muscle myosin II (NMII) is a force-generating mechanosensitive enzyme that responds to mechanical forces. NMIIs mechanoaccumulate at the cell cortex in response to mechanical forces. It is essential for cells to mechanically adapt to the physical environment, failure of which results in mitotic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504539/ https://www.ncbi.nlm.nih.gov/pubmed/37720093 http://dx.doi.org/10.1016/j.isci.2023.107773 |
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author | Wang, Chao Ding, Jingjing Wei, Qiaodong Du, Shoukang Gong, Xiaobo Chew, Ting Gang |
author_facet | Wang, Chao Ding, Jingjing Wei, Qiaodong Du, Shoukang Gong, Xiaobo Chew, Ting Gang |
author_sort | Wang, Chao |
collection | PubMed |
description | Non-muscle myosin II (NMII) is a force-generating mechanosensitive enzyme that responds to mechanical forces. NMIIs mechanoaccumulate at the cell cortex in response to mechanical forces. It is essential for cells to mechanically adapt to the physical environment, failure of which results in mitotic defects when dividing in confined environment. Much less is known about how NMII mechanoaccumulation is regulated during mitosis. We show that mitotic cells respond to compressive stress by promoting accumulation of active RhoA at the cell cortex as in interphase cells. RhoA mechanoresponse during mitosis activates and stabilizes NMIIB via ROCK signaling, leading to NMIIB mechanoaccumulation at the cell cortex. Using disease-related myosin II mutations, we found that NMIIB mechanoaccumulation requires its motor activity that translocates actin filaments, but not just its actin-binding function. Thus, the motor activity coordinates structural movement and nucleotide state changes to fine-tune actin-binding affinity optimal for NMIIs to generate and respond to forces. |
format | Online Article Text |
id | pubmed-10504539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105045392023-09-17 Mechanosensitive accumulation of non-muscle myosin IIB during mitosis requires its translocation activity Wang, Chao Ding, Jingjing Wei, Qiaodong Du, Shoukang Gong, Xiaobo Chew, Ting Gang iScience Article Non-muscle myosin II (NMII) is a force-generating mechanosensitive enzyme that responds to mechanical forces. NMIIs mechanoaccumulate at the cell cortex in response to mechanical forces. It is essential for cells to mechanically adapt to the physical environment, failure of which results in mitotic defects when dividing in confined environment. Much less is known about how NMII mechanoaccumulation is regulated during mitosis. We show that mitotic cells respond to compressive stress by promoting accumulation of active RhoA at the cell cortex as in interphase cells. RhoA mechanoresponse during mitosis activates and stabilizes NMIIB via ROCK signaling, leading to NMIIB mechanoaccumulation at the cell cortex. Using disease-related myosin II mutations, we found that NMIIB mechanoaccumulation requires its motor activity that translocates actin filaments, but not just its actin-binding function. Thus, the motor activity coordinates structural movement and nucleotide state changes to fine-tune actin-binding affinity optimal for NMIIs to generate and respond to forces. Elsevier 2023-08-29 /pmc/articles/PMC10504539/ /pubmed/37720093 http://dx.doi.org/10.1016/j.isci.2023.107773 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Wang, Chao Ding, Jingjing Wei, Qiaodong Du, Shoukang Gong, Xiaobo Chew, Ting Gang Mechanosensitive accumulation of non-muscle myosin IIB during mitosis requires its translocation activity |
title | Mechanosensitive accumulation of non-muscle myosin IIB during mitosis requires its translocation activity |
title_full | Mechanosensitive accumulation of non-muscle myosin IIB during mitosis requires its translocation activity |
title_fullStr | Mechanosensitive accumulation of non-muscle myosin IIB during mitosis requires its translocation activity |
title_full_unstemmed | Mechanosensitive accumulation of non-muscle myosin IIB during mitosis requires its translocation activity |
title_short | Mechanosensitive accumulation of non-muscle myosin IIB during mitosis requires its translocation activity |
title_sort | mechanosensitive accumulation of non-muscle myosin iib during mitosis requires its translocation activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504539/ https://www.ncbi.nlm.nih.gov/pubmed/37720093 http://dx.doi.org/10.1016/j.isci.2023.107773 |
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