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Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity
Serotonin (5-HT) is known to increase the rate of growth cone advance via cofilin-dependent increases in retrograde actin network flow and nonmuscle myosin II activity. We report that myosin II activity is regulated by PKC during 5-HT responses and that PKC activity is necessary for increases in tra...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6605792/ https://www.ncbi.nlm.nih.gov/pubmed/31123185 http://dx.doi.org/10.1083/jcb.201810054 |
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author | Zhang, Xiao-Feng Ajeti, Visar Tsai, Nicole Fereydooni, Arash Burns, William Murrell, Michael De La Cruz, Enrique M. Forscher, Paul |
author_facet | Zhang, Xiao-Feng Ajeti, Visar Tsai, Nicole Fereydooni, Arash Burns, William Murrell, Michael De La Cruz, Enrique M. Forscher, Paul |
author_sort | Zhang, Xiao-Feng |
collection | PubMed |
description | Serotonin (5-HT) is known to increase the rate of growth cone advance via cofilin-dependent increases in retrograde actin network flow and nonmuscle myosin II activity. We report that myosin II activity is regulated by PKC during 5-HT responses and that PKC activity is necessary for increases in traction force normally associated with these growth responses. 5-HT simultaneously induces cofilin-dependent decreases in actin network density and PKC-dependent increases in point contact density. These reciprocal effects facilitate increases in traction force production in domains exhibiting decreased actin network density. Interestingly, when PKC activity was up-regulated, 5-HT treatments resulted in myosin II hyperactivation accompanied by catastrophic cofilin-dependent decreases in actin filament density, sudden decreases in traction force, and neurite retraction. These results reveal a synergistic relationship between cofilin and myosin II that is spatiotemporally regulated in the growth cone via mechanocatalytic effects to modulate neurite growth. |
format | Online Article Text |
id | pubmed-6605792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66057922020-01-01 Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity Zhang, Xiao-Feng Ajeti, Visar Tsai, Nicole Fereydooni, Arash Burns, William Murrell, Michael De La Cruz, Enrique M. Forscher, Paul J Cell Biol Research Articles Serotonin (5-HT) is known to increase the rate of growth cone advance via cofilin-dependent increases in retrograde actin network flow and nonmuscle myosin II activity. We report that myosin II activity is regulated by PKC during 5-HT responses and that PKC activity is necessary for increases in traction force normally associated with these growth responses. 5-HT simultaneously induces cofilin-dependent decreases in actin network density and PKC-dependent increases in point contact density. These reciprocal effects facilitate increases in traction force production in domains exhibiting decreased actin network density. Interestingly, when PKC activity was up-regulated, 5-HT treatments resulted in myosin II hyperactivation accompanied by catastrophic cofilin-dependent decreases in actin filament density, sudden decreases in traction force, and neurite retraction. These results reveal a synergistic relationship between cofilin and myosin II that is spatiotemporally regulated in the growth cone via mechanocatalytic effects to modulate neurite growth. Rockefeller University Press 2019-07-01 2019-05-23 /pmc/articles/PMC6605792/ /pubmed/31123185 http://dx.doi.org/10.1083/jcb.201810054 Text en © 2019 Zhang et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Zhang, Xiao-Feng Ajeti, Visar Tsai, Nicole Fereydooni, Arash Burns, William Murrell, Michael De La Cruz, Enrique M. Forscher, Paul Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity |
title | Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity |
title_full | Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity |
title_fullStr | Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity |
title_full_unstemmed | Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity |
title_short | Regulation of axon growth by myosin II–dependent mechanocatalysis of cofilin activity |
title_sort | regulation of axon growth by myosin ii–dependent mechanocatalysis of cofilin activity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6605792/ https://www.ncbi.nlm.nih.gov/pubmed/31123185 http://dx.doi.org/10.1083/jcb.201810054 |
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