scholarly journals Publisher Correction: Osmotic pressure modulates single cell cycle dynamics inducing reversible growth arrest and reactivation of human metastatic cells

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Hubert M. Taïeb ◽  
Daniela S. Garske ◽  
Jörg Contzen ◽  
Manfred Gossen ◽  
Luca Bertinetti ◽  
...  
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Hubert M. Taïeb ◽  
Daniela S. Garske ◽  
Jörg Contzen ◽  
Manfred Gossen ◽  
Luca Bertinetti ◽  
...  

AbstractBiophysical cues such as osmotic pressure modulate proliferation and growth arrest of bacteria, yeast cells and seeds. In tissues, osmotic regulation takes place through blood and lymphatic capillaries and, at a single cell level, water and osmoregulation play a critical role. However, the effect of osmotic pressure on single cell cycle dynamics remains poorly understood. Here, we investigate the effect of osmotic pressure on single cell cycle dynamics, nuclear growth, proliferation, migration and protein expression, by quantitative time-lapse imaging of single cells genetically modified with fluorescent ubiquitination-based cell cycle indicator 2 (FUCCI2). Single cell data reveals that under hyperosmotic stress, distinct cell subpopulations emerge with impaired nuclear growth, delayed or growth arrested cell cycle and reduced migration. This state is reversible for mild hyperosmotic stress, where cells return to regular cell cycle dynamics, proliferation and migration. Thus, osmotic pressure can modulate the reversible growth arrest and reactivation of human metastatic cells.


2016 ◽  
Vol 130 (2) ◽  
pp. 512-520 ◽  
Author(s):  
Siang-Boon Koh ◽  
Patrice Mascalchi ◽  
Esther Rodriguez ◽  
Yao Lin ◽  
Duncan I. Jodrell ◽  
...  

Nature ◽  
2017 ◽  
Vol 547 (7661) ◽  
pp. 61-67 ◽  
Author(s):  
Takashi Nagano ◽  
Yaniv Lubling ◽  
Csilla Várnai ◽  
Carmel Dudley ◽  
Wing Leung ◽  
...  

2016 ◽  
Author(s):  
Takashi Nagano ◽  
Yaniv Lubling ◽  
Csilla Varnai ◽  
Carmel Dudley ◽  
Wing Leung ◽  
...  

SummaryChromosomes in proliferating metazoan cells undergo dramatic structural metamorphoses every cell cycle, alternating between a highly condensed mitotic structure facilitating chromosome segregation, and a decondensed interphase structure accommodating transcription, gene silencing and DNA replication. These cyclical structural transformations have been evident under the microscope for over a century, but their molecular-level analysis is still lacking. Here we use single-cell Hi-C to study chromosome conformations in thousands of individual cells, and discover a continuum of cis-interaction profiles that finely position individual cells along the cell cycle. We show that chromosomal compartments, topological domains (TADs), contact insulation and long-range loops, all defined by ensemble Hi-C maps, are governed by distinct cell cycle dynamics. In particular, DNA replication correlates with build-up of compartments and reduction in TAD insulation, while loops are generally stable from G1 through S and G2. Analysing whole genome 3D structural models using haploid cell data, we discover a radial architecture of chromosomal compartments with distinct epigenomic signatures. Our single-cell data creates an essential new paradigm for the re-interpretation of chromosome conformation maps through the prism of the cell cycle.


2003 ◽  
Vol 43 (supplement) ◽  
pp. S113
Author(s):  
K. Matsumura ◽  
T. Yagi ◽  
K. Yasuda

Cell Cycle ◽  
2010 ◽  
Vol 9 (1) ◽  
pp. 121-130 ◽  
Author(s):  
Rachel J. Errington ◽  
Martyn R. Brown ◽  
Oscar Silvestre ◽  
Kerenza L. Njoh ◽  
Sally C. Chappell ◽  
...  

2002 ◽  
Vol 363 (3) ◽  
pp. 431-436 ◽  
Author(s):  
Or KAKHLON ◽  
Yosef GRUENBAUM ◽  
Z. Ioav CABANTCHIK

Repression or overexpression of ferritin accelerated or retarded cell cycling respectively, via changes in the cellular labile iron pool (LIP). A rise in LIP is caused by ferritin repression enhanced growth, induced by H-ras, and reverted growth arrest is induced by dominant negative H-ras. The studies indicate that repression of ferritin expression provides a mechanism by which certain oncogenes lead to cell growth stimulation.


Nature ◽  
2015 ◽  
Vol 519 (7544) ◽  
pp. 468-471 ◽  
Author(s):  
Oded Sandler ◽  
Sivan Pearl Mizrahi ◽  
Noga Weiss ◽  
Oded Agam ◽  
Itamar Simon ◽  
...  

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