Vianay Benoit, Senger Fabrice, Alamos Simon, Anjur-Dietrich Maya, Bearce Elizabeth, Cheeseman Bevan, Lee Lisa, Théry Manuel
University of Paris Diderot, INSERM, CEA, Hôpital Saint Louis, Institut Universitaire d'Hematologie, UMRS1160, CytoMorpho Lab, 75010, Paris, France.
University of Grenoble-Alpes, CEA, CNRS, INRA, Biosciences & Biotechnology Institute of Grenoble, Laboratoire de Phyiologie Cellulaire & Végétale, CytoMorpho Lab, 38054, Grenoble, France.
Biol Cell. 2018 Apr;110(4):91-96. doi: 10.1111/boc.201800006. Epub 2018 Mar 12.
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.
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.
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.
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.
组织形态发生源于细胞生长与机械力之间的相互作用。虽然几何限制和机械力对细胞增殖的影响已得到相当充分的表征,但这种反向关系却了解得少得多。在此,我们研究了在细胞周期进程中牵引力如何变化。
为了区分细胞收缩性变化与细胞大小增加,细胞形状在微图案化底物上受到限制。我们对表达细胞周期报告基因的异步分裂细胞进行了牵引力测量,以获取细胞分裂过程中产生的收缩力测量值。我们发现,随着细胞在G1期进程中,力趋于增加,在S期达到平稳状态,然后在G2期下降。
虽然在细胞周期进程中细胞大小有规律地增加,但牵引力基于细胞在早期和晚期生长阶段收缩性的特定且相反调节呈现双相行为。
这些结果突出了细胞信号传导在调节细胞收缩性中的关键作用,与细胞大小和形状无关。细胞周期进程中细胞收缩性的非单调变化可能以复杂且非线性的方式影响组织稳态的机械调节。