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External forces control mitotic spindle positioning

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TLDR
It is found that forces applied on the cell body direct spindle orientation during mitosis, and it is proposed that cells divide according to cues provided by their mechanical micro-environment, aligning daughter cells with the external force field.
Abstract
The response of cells to forces is essential for tissue morphogenesis and homeostasis. This response has been extensively investigated in interphase cells, but it remains unclear how forces affect dividing cells. We used a combination of micro-manipulation tools on human dividing cells to address the role of physical parameters of the micro-environment in controlling the cell division axis, a key element of tissue morphogenesis. We found that forces applied on the cell body direct spindle orientation during mitosis. We further show that external constraints induce a polarization of dynamic subcortical actin structures that correlate with spindle movements. We propose that cells divide according to cues provided by their mechanical micro-environment, aligning daughter cells with the external force field.

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Nanoscale surfaces for the long-term maintenance of mesenchymal stem cell phenotype and multipotency

TL;DR: The study identifies a nanostructured surface that retains stem-cell phenotype and maintains stem- cell growth over eight weeks, and implicates a role for small RNAs in repressing key cell signalling and metabolomic pathways, demonstrating the potential of surfaces as non-invasive tools with which to address the stem cell niche.
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Cellular mechanotransduction: From tension to function

TL;DR: A critical review of the recent insights into the molecular basis of cellular mechanotransduction is provided, by analyzing how mechanical stimuli get transformed into a given biological response through the activation of a peculiar genetic program.
Journal ArticleDOI

The Centrosome in Cells and Organisms

TL;DR: The role of the centrosomes in cell polarity, resulting from its ability to position the nucleus at the cell center, is discussed and how centrosome innovation might have been critical during metazoan evolution is discussed.
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Mechanobiology and developmental control.

TL;DR: Work that has revealed the central role that physical forces and extracellular matrix mechanics play in the control of cell fate switching, pattern formation, and tissue development in the embryo is reviewed and how these same mechanical signals contribute to tissue homeostasis and developmental control throughout adult life is reviewed.
References
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Journal ArticleDOI

Local force and geometry sensing regulate cell functions.

TL;DR: Tissue scaffolds that have been engineered at the micro- and nanoscale level now enable better dissection of the mechanosensing, transduction and response mechanisms of eukaryotic cells.
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Lifeact: a versatile marker to visualize F-actin

TL;DR: Lifeact, a 17-amino-acid peptide, is described, which stained filamentous actin (F-actin) structures in eukaryotic cells and tissues and in its chemically modified peptide form allowed visualization of actin dynamics in nontransfectable cells.
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Demonstration of mechanical connections between integrins, cytoskeletal filaments, and nucleoplasm that stabilize nuclear structure

TL;DR: Molecular connections between integrins, cytoskeletal filaments, and nuclear scaffolds may provide a discrete path for mechanical signal transfer through cells as well as a mechanism for producing integrated changes in cell and nuclear structure in response to changes in extracellular matrix adhesivity or mechanics.
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The Influence of Cell Mechanics, Cell-Cell Interactions, and Proliferation on Epithelial Packing

TL;DR: A vertex model is used for the epithelial junctional network in which cell packing geometries correspond to stable and stationary network configurations and accounts qualitatively and quantitatively for the observed packing geometry in the wing disc and its response to perturbation by laser ablation.
Journal ArticleDOI

The optical stretcher: a novel laser tool to micromanipulate cells.

TL;DR: The magnitude of the deforming forces in the optical stretcher bridges the gap between optical tweezers and atomic force microscopy for the study of biologic materials.
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