Multiplex profiling of cellular invasion in 3D cell culture models.

To-date, most invasion or migration assays use a modified Boyden chamber-like design to assess migration as single-cell or scratch assays on coated or uncoated planar plastic surfaces. Here, we describe a 96-well microplate-based, high-content, three-dimensional cell culture assay capable of assessi...

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Main Authors: Gerald Burgstaller, Bettina Oehrle, Ina Koch, Michael Lindner, Oliver Eickelberg
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23671660/?tool=EBI
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spelling doaj-1a4301e54d784a8c842c7f3cdbda79fa2021-03-03T20:23:17ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0185e6312110.1371/journal.pone.0063121Multiplex profiling of cellular invasion in 3D cell culture models.Gerald BurgstallerBettina OehrleIna KochMichael LindnerOliver EickelbergTo-date, most invasion or migration assays use a modified Boyden chamber-like design to assess migration as single-cell or scratch assays on coated or uncoated planar plastic surfaces. Here, we describe a 96-well microplate-based, high-content, three-dimensional cell culture assay capable of assessing invasion dynamics and molecular signatures thereof. On applying our invasion assay, we were able to demonstrate significant effects on the invasion capacity of fibroblast cell lines, as well as primary lung fibroblasts. Administration of epidermal growth factor resulted in a substantial increase of cellular invasion, thus making this technique suitable for high-throughput pharmacological screening of novel compounds regulating invasive and migratory pathways of primary cells. Our assay also correlates cellular invasiveness to molecular events. Thus, we argue of having developed a powerful and versatile toolbox for an extensive profiling of invasive cells in a 96-well format. This will have a major impact on research in disease areas like fibrosis, metastatic cancers, or chronic inflammatory states.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23671660/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Gerald Burgstaller
Bettina Oehrle
Ina Koch
Michael Lindner
Oliver Eickelberg
spellingShingle Gerald Burgstaller
Bettina Oehrle
Ina Koch
Michael Lindner
Oliver Eickelberg
Multiplex profiling of cellular invasion in 3D cell culture models.
PLoS ONE
author_facet Gerald Burgstaller
Bettina Oehrle
Ina Koch
Michael Lindner
Oliver Eickelberg
author_sort Gerald Burgstaller
title Multiplex profiling of cellular invasion in 3D cell culture models.
title_short Multiplex profiling of cellular invasion in 3D cell culture models.
title_full Multiplex profiling of cellular invasion in 3D cell culture models.
title_fullStr Multiplex profiling of cellular invasion in 3D cell culture models.
title_full_unstemmed Multiplex profiling of cellular invasion in 3D cell culture models.
title_sort multiplex profiling of cellular invasion in 3d cell culture models.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description To-date, most invasion or migration assays use a modified Boyden chamber-like design to assess migration as single-cell or scratch assays on coated or uncoated planar plastic surfaces. Here, we describe a 96-well microplate-based, high-content, three-dimensional cell culture assay capable of assessing invasion dynamics and molecular signatures thereof. On applying our invasion assay, we were able to demonstrate significant effects on the invasion capacity of fibroblast cell lines, as well as primary lung fibroblasts. Administration of epidermal growth factor resulted in a substantial increase of cellular invasion, thus making this technique suitable for high-throughput pharmacological screening of novel compounds regulating invasive and migratory pathways of primary cells. Our assay also correlates cellular invasiveness to molecular events. Thus, we argue of having developed a powerful and versatile toolbox for an extensive profiling of invasive cells in a 96-well format. This will have a major impact on research in disease areas like fibrosis, metastatic cancers, or chronic inflammatory states.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23671660/?tool=EBI
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