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Actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle

The Par complex directs fate-determinant segregation from the apical membrane of asymmetrically dividing Drosophila neuroblasts. While the physical interactions that recruit the Par complex have been extensively studied, little is known about how the membrane itself behaves during polarization. We e...

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Detalles Bibliográficos
Autores principales: LaFoya, Bryce, Prehoda, Kenneth E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174105/
https://www.ncbi.nlm.nih.gov/pubmed/34010656
http://dx.doi.org/10.1016/j.celrep.2021.109146
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author LaFoya, Bryce
Prehoda, Kenneth E.
author_facet LaFoya, Bryce
Prehoda, Kenneth E.
author_sort LaFoya, Bryce
collection PubMed
description The Par complex directs fate-determinant segregation from the apical membrane of asymmetrically dividing Drosophila neuroblasts. While the physical interactions that recruit the Par complex have been extensively studied, little is known about how the membrane itself behaves during polarization. We examined the membrane dynamics of neuroblasts and surrounding cells using a combination of super-resolution and time-lapse imaging, revealing cellular-scale movements of diverse membrane features during asymmetric division cycles. Membrane domains that are distributed across the neuroblast membrane in interphase become polarized in early mitosis, where they mediate formation of cortical patches of the Par protein atypical protein kinase C (aPKC). Membrane and protein polarity cycles are precisely synchronized and are generated by extensive actin-dependent forces that deform the surrounding tissue. In addition to suggesting a role for the membrane in asymmetric division, our results reveal the mechanical nature of the neuroblast polarity cycle.
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spelling pubmed-81741052021-06-03 Actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle LaFoya, Bryce Prehoda, Kenneth E. Cell Rep Article The Par complex directs fate-determinant segregation from the apical membrane of asymmetrically dividing Drosophila neuroblasts. While the physical interactions that recruit the Par complex have been extensively studied, little is known about how the membrane itself behaves during polarization. We examined the membrane dynamics of neuroblasts and surrounding cells using a combination of super-resolution and time-lapse imaging, revealing cellular-scale movements of diverse membrane features during asymmetric division cycles. Membrane domains that are distributed across the neuroblast membrane in interphase become polarized in early mitosis, where they mediate formation of cortical patches of the Par protein atypical protein kinase C (aPKC). Membrane and protein polarity cycles are precisely synchronized and are generated by extensive actin-dependent forces that deform the surrounding tissue. In addition to suggesting a role for the membrane in asymmetric division, our results reveal the mechanical nature of the neuroblast polarity cycle. 2021-05-18 /pmc/articles/PMC8174105/ /pubmed/34010656 http://dx.doi.org/10.1016/j.celrep.2021.109146 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
LaFoya, Bryce
Prehoda, Kenneth E.
Actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle
title Actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle
title_full Actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle
title_fullStr Actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle
title_full_unstemmed Actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle
title_short Actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle
title_sort actin-dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174105/
https://www.ncbi.nlm.nih.gov/pubmed/34010656
http://dx.doi.org/10.1016/j.celrep.2021.109146
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