Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Xiao-Feng, Ajeti, Visar, Tsai, Nicole, Fereydooni, Arash, Burns, William, Murrell, Michael, De La Cruz, Enrique M., Forscher, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
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
_version_ 1783431830249144320
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
work_keys_str_mv AT zhangxiaofeng regulationofaxongrowthbymyosiniidependentmechanocatalysisofcofilinactivity
AT ajetivisar regulationofaxongrowthbymyosiniidependentmechanocatalysisofcofilinactivity
AT tsainicole regulationofaxongrowthbymyosiniidependentmechanocatalysisofcofilinactivity
AT fereydooniarash regulationofaxongrowthbymyosiniidependentmechanocatalysisofcofilinactivity
AT burnswilliam regulationofaxongrowthbymyosiniidependentmechanocatalysisofcofilinactivity
AT murrellmichael regulationofaxongrowthbymyosiniidependentmechanocatalysisofcofilinactivity
AT delacruzenriquem regulationofaxongrowthbymyosiniidependentmechanocatalysisofcofilinactivity
AT forscherpaul regulationofaxongrowthbymyosiniidependentmechanocatalysisofcofilinactivity