Literature DB >> 27684088

Ordering Single Cells and Single Embryos in 3D Confinement: A New Device for High Content Screening.

Viktoria Wollrab1, David Caballero1, Raghavan Thiagarajan1, Daniel Riveline2.   

Abstract

Biological cells are usually observed on flat (2D) surfaces. This condition is not physiological, and phenotypes and shapes are highly variable. Screening based on cells in such environments have therefore serious limitations: cell organelles show extreme phenotypes, cell morphologies and sizes are heterogeneous and/or specific cell organelles cannot be properly visualized. In addition, cells in vivo are located in a 3D environment; in this situation, cells show different phenotypes mainly because of their interaction with the surrounding extracellular matrix of the tissue. In order to standardize and generate order of single cells in a physiologically-relevant 3D environment for cell-based assays, we report here the microfabrication and applications of a device for in vitro 3D cell culture. This device consists of a 2D array of microcavities (typically 10(5) cavities/cm(2)), each filled with single cells or embryos. Cell position, shape, polarity and internal cell organization become then normalized showing a 3D architecture. We used replica molding to pattern an array of microcavities, 'eggcups', onto a thin polydimethylsiloxane (PDMS) layer adhered on a coverslip. Cavities were covered with fibronectin to facilitate adhesion. Cells were inserted by centrifugation. Filling percentage was optimized for each system allowing up to 80%. Cells and embryos viability was confirmed. We applied this methodology for the visualization of cellular organelles, such as nucleus and Golgi apparatus, and to study active processes, such as the closure of the cytokinetic ring during cell mitosis. This device allowed the identification of new features, such as periodic accumulations and inhomogeneities of myosin and actin during the cytokinetic ring closure and compacted phenotypes for Golgi and nucleus alignment. We characterized the method for mammalian cells, fission yeast, budding yeast, C. elegans with specific adaptation in each case. Finally, the characteristics of this device make it particularly interesting for drug screening assays and personalized medicine.

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Mesh:

Year:  2016        PMID: 27684088      PMCID: PMC5092031          DOI: 10.3791/51880

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  26 in total

1.  Dissecting temporal and spatial control of cytokinesis with a myosin II Inhibitor.

Authors:  Aaron F Straight; Amy Cheung; John Limouze; Irene Chen; Nick J Westwood; James R Sellers; Timothy J Mitchison
Journal:  Science       Date:  2003-03-14       Impact factor: 47.728

2.  MITOTICALLY SYNCHRONIZED MAMMALIAN CELLS: A SIMPLE METHOD FOR OBTAINING LARGE POPULATIONS.

Authors:  E ROBBINS; P I MARCUS
Journal:  Science       Date:  1964-05-29       Impact factor: 47.728

Review 3.  High content screening: seeing is believing.

Authors:  Fabian Zanella; James B Lorens; Wolfgang Link
Journal:  Trends Biotechnol       Date:  2010-03-24       Impact factor: 19.536

4.  Mechanics of cell spreading within 3D-micropatterned environments.

Authors:  Marion Ghibaudo; Jean-Marc Di Meglio; Pascal Hersen; Benoit Ladoux
Journal:  Lab Chip       Date:  2010-12-06       Impact factor: 6.799

Review 5.  Microfluidic cell culture.

Authors:  Matthias Mehling; Savaş Tay
Journal:  Curr Opin Biotechnol       Date:  2013-11-12       Impact factor: 9.740

6.  Taking cell-matrix adhesions to the third dimension.

Authors:  E Cukierman; R Pankov; D R Stevens; K M Yamada
Journal:  Science       Date:  2001-11-23       Impact factor: 47.728

7.  Basic Caenorhabditis elegans methods: synchronization and observation.

Authors:  Montserrat Porta-de-la-Riva; Laura Fontrodona; Alberto Villanueva; Julián Cerón
Journal:  J Vis Exp       Date:  2012-06-10       Impact factor: 1.355

Review 8.  Evaluating drug efficacy and toxicology in three dimensions: using synthetic extracellular matrices in drug discovery.

Authors:  Glenn D Prestwich
Journal:  Acc Chem Res       Date:  2007-07-27       Impact factor: 22.384

9.  Generation of cell-free extracts of Xenopus eggs and demembranated sperm chromatin for the assembly and isolation of in vitro-formed nuclei for Western blotting and scanning electron microscopy (SEM).

Authors:  T D Allen; S A Rutherford; S Murray; H S Sanderson; F Gardiner; E Kiseleva; M W Goldberg; S P Drummond
Journal:  Nat Protoc       Date:  2007       Impact factor: 13.491

10.  Anillin-related protein Mid1p coordinates the assembly of the cytokinetic contractile ring in fission yeast.

Authors:  Shambaditya Saha; Thomas D Pollard
Journal:  Mol Biol Cell       Date:  2012-08-23       Impact factor: 4.138

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