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Epithelial layer unjamming shifts energy metabolism toward glycolysis

In development of an embryo, healing of a wound, or progression of a carcinoma, a requisite event is collective epithelial cellular migration. For example, cells at the advancing front of a wound edge tend to migrate collectively, elongate substantially, and exert tractions more forcefully compared...

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Autores principales: DeCamp, Stephen J., Tsuda, Victor M. K., Ferruzzi, Jacopo, Koehler, Stephan A., Giblin, John T., Roblyer, Darren, Zaman, Muhammad H., Weiss, Scott T., Kılıç, Ayşe, De Marzio, Margherita, Park, Chan Young, Ogassavara, Nicolas Chiu, Mitchel, Jennifer A., Butler, James P., Fredberg, Jeffrey J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591531/
https://www.ncbi.nlm.nih.gov/pubmed/33110128
http://dx.doi.org/10.1038/s41598-020-74992-z
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author DeCamp, Stephen J.
Tsuda, Victor M. K.
Ferruzzi, Jacopo
Koehler, Stephan A.
Giblin, John T.
Roblyer, Darren
Zaman, Muhammad H.
Weiss, Scott T.
Kılıç, Ayşe
De Marzio, Margherita
Park, Chan Young
Ogassavara, Nicolas Chiu
Mitchel, Jennifer A.
Butler, James P.
Fredberg, Jeffrey J.
author_facet DeCamp, Stephen J.
Tsuda, Victor M. K.
Ferruzzi, Jacopo
Koehler, Stephan A.
Giblin, John T.
Roblyer, Darren
Zaman, Muhammad H.
Weiss, Scott T.
Kılıç, Ayşe
De Marzio, Margherita
Park, Chan Young
Ogassavara, Nicolas Chiu
Mitchel, Jennifer A.
Butler, James P.
Fredberg, Jeffrey J.
author_sort DeCamp, Stephen J.
collection PubMed
description In development of an embryo, healing of a wound, or progression of a carcinoma, a requisite event is collective epithelial cellular migration. For example, cells at the advancing front of a wound edge tend to migrate collectively, elongate substantially, and exert tractions more forcefully compared with cells many ranks behind. With regards to energy metabolism, striking spatial gradients have recently been reported in the wounded epithelium, as well as in the tumor, but within the wounded cell layer little is known about the link between mechanical events and underlying energy metabolism. Using the advancing confluent monolayer of MDCKII cells as a model system, here we report at single cell resolution the evolving spatiotemporal fields of cell migration speeds, cell shapes, and traction forces measured simultaneously with fields of multiple indices of cellular energy metabolism. Compared with the epithelial layer that is unwounded, which is non-migratory, solid-like and jammed, the leading edge of the advancing cell layer is shown to become progressively more migratory, fluid-like, and unjammed. In doing so the cytoplasmic redox ratio becomes progressively smaller, the NADH lifetime becomes progressively shorter, and the mitochondrial membrane potential and glucose uptake become progressively larger. These observations indicate that a metabolic shift toward glycolysis accompanies collective cellular migration but show, further, that this shift occurs throughout the cell layer, even in regions where associated changes in cell shapes, traction forces, and migration velocities have yet to penetrate. In characterizing the wound healing process these morphological, mechanical, and metabolic observations, taken on a cell-by-cell basis, comprise the most comprehensive set of biophysical data yet reported. Together, these data suggest the novel hypothesis that the unjammed phase evolved to accommodate fluid-like migratory dynamics during episodes of tissue wound healing, development, and plasticity, but is more energetically expensive compared with the jammed phase, which evolved to maintain a solid-like non-migratory state that is more energetically economical.
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spelling pubmed-75915312020-10-28 Epithelial layer unjamming shifts energy metabolism toward glycolysis DeCamp, Stephen J. Tsuda, Victor M. K. Ferruzzi, Jacopo Koehler, Stephan A. Giblin, John T. Roblyer, Darren Zaman, Muhammad H. Weiss, Scott T. Kılıç, Ayşe De Marzio, Margherita Park, Chan Young Ogassavara, Nicolas Chiu Mitchel, Jennifer A. Butler, James P. Fredberg, Jeffrey J. Sci Rep Article In development of an embryo, healing of a wound, or progression of a carcinoma, a requisite event is collective epithelial cellular migration. For example, cells at the advancing front of a wound edge tend to migrate collectively, elongate substantially, and exert tractions more forcefully compared with cells many ranks behind. With regards to energy metabolism, striking spatial gradients have recently been reported in the wounded epithelium, as well as in the tumor, but within the wounded cell layer little is known about the link between mechanical events and underlying energy metabolism. Using the advancing confluent monolayer of MDCKII cells as a model system, here we report at single cell resolution the evolving spatiotemporal fields of cell migration speeds, cell shapes, and traction forces measured simultaneously with fields of multiple indices of cellular energy metabolism. Compared with the epithelial layer that is unwounded, which is non-migratory, solid-like and jammed, the leading edge of the advancing cell layer is shown to become progressively more migratory, fluid-like, and unjammed. In doing so the cytoplasmic redox ratio becomes progressively smaller, the NADH lifetime becomes progressively shorter, and the mitochondrial membrane potential and glucose uptake become progressively larger. These observations indicate that a metabolic shift toward glycolysis accompanies collective cellular migration but show, further, that this shift occurs throughout the cell layer, even in regions where associated changes in cell shapes, traction forces, and migration velocities have yet to penetrate. In characterizing the wound healing process these morphological, mechanical, and metabolic observations, taken on a cell-by-cell basis, comprise the most comprehensive set of biophysical data yet reported. Together, these data suggest the novel hypothesis that the unjammed phase evolved to accommodate fluid-like migratory dynamics during episodes of tissue wound healing, development, and plasticity, but is more energetically expensive compared with the jammed phase, which evolved to maintain a solid-like non-migratory state that is more energetically economical. Nature Publishing Group UK 2020-10-27 /pmc/articles/PMC7591531/ /pubmed/33110128 http://dx.doi.org/10.1038/s41598-020-74992-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
DeCamp, Stephen J.
Tsuda, Victor M. K.
Ferruzzi, Jacopo
Koehler, Stephan A.
Giblin, John T.
Roblyer, Darren
Zaman, Muhammad H.
Weiss, Scott T.
Kılıç, Ayşe
De Marzio, Margherita
Park, Chan Young
Ogassavara, Nicolas Chiu
Mitchel, Jennifer A.
Butler, James P.
Fredberg, Jeffrey J.
Epithelial layer unjamming shifts energy metabolism toward glycolysis
title Epithelial layer unjamming shifts energy metabolism toward glycolysis
title_full Epithelial layer unjamming shifts energy metabolism toward glycolysis
title_fullStr Epithelial layer unjamming shifts energy metabolism toward glycolysis
title_full_unstemmed Epithelial layer unjamming shifts energy metabolism toward glycolysis
title_short Epithelial layer unjamming shifts energy metabolism toward glycolysis
title_sort epithelial layer unjamming shifts energy metabolism toward glycolysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591531/
https://www.ncbi.nlm.nih.gov/pubmed/33110128
http://dx.doi.org/10.1038/s41598-020-74992-z
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