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Variation in traction forces during cell cycle progression

Background Information Tissue morphogenesis results from the interplay between cell growth and mechanical forces. While the impact of geometrical confinement and mechanical forces on cell proliferation has been fairly well characterised, the inverse relationship is much less understood. Here, we inv...

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Published in:Biology of the cell 2018-04, Vol.110 (4), p.91-96
Main Authors: Vianay, Benoit, Senger, Fabrice, Alamos, Simon, Anjur‐Dietrich, Maya, Bearce, Elizabeth, Cheeseman, Bevan, Lee, Lisa, Théry, Manuel
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cited_by cdi_FETCH-LOGICAL-c4806-21f2d21e66c84d8f0187d37b1f3441ed39e116f42795f6ed9f49b960bcb92b1f3
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container_end_page 96
container_issue 4
container_start_page 91
container_title Biology of the cell
container_volume 110
creator Vianay, Benoit
Senger, Fabrice
Alamos, Simon
Anjur‐Dietrich, Maya
Bearce, Elizabeth
Cheeseman, Bevan
Lee, Lisa
Théry, Manuel
description Background Information Tissue morphogenesis results from the interplay between cell growth and mechanical forces. While the impact of geometrical confinement and mechanical forces on cell proliferation has been fairly well characterised, the inverse relationship is much less understood. Here, we investigated how traction forces vary during cell cycle progression. Results Cell shape was constrained on micropatterned substrates in order to distinguish variations in cell contractility from cell size increase. We performed traction force measurements of asynchronously dividing cells expressing a cell‐cycle reporter, to obtain measurements of contractile forces generated during cell division. We found that forces tend to increase as cells progress through G1, before reaching a plateau in S phase, and then decline during G2. Conclusions While cell size increases regularly during cell cycle progression, traction forces follow a biphasic behaviour based on specific and opposite regulation of cell contractility during early and late growth phases. Significance These results highlight the key role of cellular signalling in the regulation of cell contractility, independently of cell size and shape. Non‐monotonous variations of cell contractility during cell cycle progression are likely to impact the mechanical regulation of tissue homoeostasis in a complex and non‐linear manner. Short Communication This manuscript compares cell traction forces according to their position in their cell cycle. It shows that forces increase from early G1 to S phase. It then reveals an unexpected decrease of traction forces from S to G2.
doi_str_mv 10.1111/boc.201800006
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While the impact of geometrical confinement and mechanical forces on cell proliferation has been fairly well characterised, the inverse relationship is much less understood. Here, we investigated how traction forces vary during cell cycle progression. Results Cell shape was constrained on micropatterned substrates in order to distinguish variations in cell contractility from cell size increase. We performed traction force measurements of asynchronously dividing cells expressing a cell‐cycle reporter, to obtain measurements of contractile forces generated during cell division. We found that forces tend to increase as cells progress through G1, before reaching a plateau in S phase, and then decline during G2. Conclusions While cell size increases regularly during cell cycle progression, traction forces follow a biphasic behaviour based on specific and opposite regulation of cell contractility during early and late growth phases. Significance These results highlight the key role of cellular signalling in the regulation of cell contractility, independently of cell size and shape. Non‐monotonous variations of cell contractility during cell cycle progression are likely to impact the mechanical regulation of tissue homoeostasis in a complex and non‐linear manner. Short Communication This manuscript compares cell traction forces according to their position in their cell cycle. It shows that forces increase from early G1 to S phase. It then reveals an unexpected decrease of traction forces from S to G2.</description><identifier>ISSN: 0248-4900</identifier><identifier>EISSN: 1768-322X</identifier><identifier>DOI: 10.1111/boc.201800006</identifier><identifier>PMID: 29388708</identifier><language>eng</language><publisher>England: Wiley</publisher><subject>Cell cycle ; Cell mechanics ; Cellular Biology ; Life Sciences ; Traction forces</subject><ispartof>Biology of the cell, 2018-04, Vol.110 (4), p.91-96</ispartof><rights>2018 Société Française des Microscopies and Société de Biologie Cellulaire de France. Published by John Wiley &amp; Sons Ltd</rights><rights>2018 Société Française des Microscopies and Société de Biologie Cellulaire de France. 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While the impact of geometrical confinement and mechanical forces on cell proliferation has been fairly well characterised, the inverse relationship is much less understood. Here, we investigated how traction forces vary during cell cycle progression. Results Cell shape was constrained on micropatterned substrates in order to distinguish variations in cell contractility from cell size increase. We performed traction force measurements of asynchronously dividing cells expressing a cell‐cycle reporter, to obtain measurements of contractile forces generated during cell division. We found that forces tend to increase as cells progress through G1, before reaching a plateau in S phase, and then decline during G2. Conclusions While cell size increases regularly during cell cycle progression, traction forces follow a biphasic behaviour based on specific and opposite regulation of cell contractility during early and late growth phases. Significance These results highlight the key role of cellular signalling in the regulation of cell contractility, independently of cell size and shape. Non‐monotonous variations of cell contractility during cell cycle progression are likely to impact the mechanical regulation of tissue homoeostasis in a complex and non‐linear manner. Short Communication This manuscript compares cell traction forces according to their position in their cell cycle. It shows that forces increase from early G1 to S phase. 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subjects Cell cycle
Cell mechanics
Cellular Biology
Life Sciences
Traction forces
title Variation in traction forces during cell cycle progression
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