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Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation

Post-translational modification of tubulin provides differential functions to microtubule networks. Here, we address the role of tubulin acetylation on the penetrative capacity of cells undergoing radial intercalation, which is the process by which cells move apically, insert between outer cells, an...

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Detalles Bibliográficos
Autores principales: Collins, Caitlin, Kim, Sun K., Ventrella, Rosa, Carruzzo, Herve M., Wortman, Juliana C., Han, Hyebin, Suva, Evelyn E., Mitchell, Jennifer W., Yu, Clare C., Mitchell, Brian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383821/
https://www.ncbi.nlm.nih.gov/pubmed/34407402
http://dx.doi.org/10.1016/j.celrep.2021.109556
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author Collins, Caitlin
Kim, Sun K.
Ventrella, Rosa
Carruzzo, Herve M.
Wortman, Juliana C.
Han, Hyebin
Suva, Evelyn E.
Mitchell, Jennifer W.
Yu, Clare C.
Mitchell, Brian J.
author_facet Collins, Caitlin
Kim, Sun K.
Ventrella, Rosa
Carruzzo, Herve M.
Wortman, Juliana C.
Han, Hyebin
Suva, Evelyn E.
Mitchell, Jennifer W.
Yu, Clare C.
Mitchell, Brian J.
author_sort Collins, Caitlin
collection PubMed
description Post-translational modification of tubulin provides differential functions to microtubule networks. Here, we address the role of tubulin acetylation on the penetrative capacity of cells undergoing radial intercalation, which is the process by which cells move apically, insert between outer cells, and join an epithelium. There are opposing forces that regulate intercalation, namely, the restrictive forces of the epithelial barrier versus the penetrative forces of the intercalating cell. Positively and negatively modulating tubulin acetylation in intercalating cells alters the developmental timing such that cells with more acetylation penetrate faster. We find that intercalating cells preferentially penetrate higher-order vertices rather than the more prevalent tricellular vertices. Differential timing in the ability of cells to penetrate different vertices reveals that lower-order vertices represent more restrictive sites of insertion. We shift the accessibility of intercalating cells toward more restrictive junctions by increasing tubulin acetylation, and we provide a geometric-based mathematical model that describes our results.
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spelling pubmed-83838212021-08-24 Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation Collins, Caitlin Kim, Sun K. Ventrella, Rosa Carruzzo, Herve M. Wortman, Juliana C. Han, Hyebin Suva, Evelyn E. Mitchell, Jennifer W. Yu, Clare C. Mitchell, Brian J. Cell Rep Article Post-translational modification of tubulin provides differential functions to microtubule networks. Here, we address the role of tubulin acetylation on the penetrative capacity of cells undergoing radial intercalation, which is the process by which cells move apically, insert between outer cells, and join an epithelium. There are opposing forces that regulate intercalation, namely, the restrictive forces of the epithelial barrier versus the penetrative forces of the intercalating cell. Positively and negatively modulating tubulin acetylation in intercalating cells alters the developmental timing such that cells with more acetylation penetrate faster. We find that intercalating cells preferentially penetrate higher-order vertices rather than the more prevalent tricellular vertices. Differential timing in the ability of cells to penetrate different vertices reveals that lower-order vertices represent more restrictive sites of insertion. We shift the accessibility of intercalating cells toward more restrictive junctions by increasing tubulin acetylation, and we provide a geometric-based mathematical model that describes our results. 2021-08-17 /pmc/articles/PMC8383821/ /pubmed/34407402 http://dx.doi.org/10.1016/j.celrep.2021.109556 Text en 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/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Collins, Caitlin
Kim, Sun K.
Ventrella, Rosa
Carruzzo, Herve M.
Wortman, Juliana C.
Han, Hyebin
Suva, Evelyn E.
Mitchell, Jennifer W.
Yu, Clare C.
Mitchell, Brian J.
Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation
title Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation
title_full Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation
title_fullStr Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation
title_full_unstemmed Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation
title_short Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation
title_sort tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383821/
https://www.ncbi.nlm.nih.gov/pubmed/34407402
http://dx.doi.org/10.1016/j.celrep.2021.109556
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