Neural cell 3D microtissue formation is marked by cytokines' up-regulation.

Cells cultured in three dimensional (3D) scaffolds as opposed to traditional two-dimensional (2D) substrates have been considered more physiologically relevant based on their superior ability to emulate the in vivo environment. Combined with stem cell technology, 3D cell cultures can provide a promi...

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Main Authors: Yinzhi Lai, Amish Asthana, Ke Cheng, William S Kisaalita
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3203927?pdf=render
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spelling doaj-0febc946bb3f4e81a939be1b1e6a29872020-11-25T01:48:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2682110.1371/journal.pone.0026821Neural cell 3D microtissue formation is marked by cytokines' up-regulation.Yinzhi LaiAmish AsthanaKe ChengWilliam S KisaalitaCells cultured in three dimensional (3D) scaffolds as opposed to traditional two-dimensional (2D) substrates have been considered more physiologically relevant based on their superior ability to emulate the in vivo environment. Combined with stem cell technology, 3D cell cultures can provide a promising alternative for use in cell-based assays or biosensors in non-clinical drug discovery studies. To advance 3D culture technology, a case has been made for identifying and validating three-dimensionality biomarkers. With this goal in mind, we conducted a transcriptomic expression comparison among neural progenitor cells cultured on 2D substrates, 3D porous polystyrene scaffolds, and as 3D neurospheres (in vivo surrogate). Up-regulation of cytokines as a group in 3D and neurospheres was observed. A group of 13 cytokines were commonly up-regulated in cells cultured in polystyrene scaffolds and neurospheres, suggesting potential for any or a combination from this list to serve as three-dimensionality biomarkers. These results are supportive of further cytokine identification and validation studies with cells from non-neural tissue.http://europepmc.org/articles/PMC3203927?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yinzhi Lai
Amish Asthana
Ke Cheng
William S Kisaalita
spellingShingle Yinzhi Lai
Amish Asthana
Ke Cheng
William S Kisaalita
Neural cell 3D microtissue formation is marked by cytokines' up-regulation.
PLoS ONE
author_facet Yinzhi Lai
Amish Asthana
Ke Cheng
William S Kisaalita
author_sort Yinzhi Lai
title Neural cell 3D microtissue formation is marked by cytokines' up-regulation.
title_short Neural cell 3D microtissue formation is marked by cytokines' up-regulation.
title_full Neural cell 3D microtissue formation is marked by cytokines' up-regulation.
title_fullStr Neural cell 3D microtissue formation is marked by cytokines' up-regulation.
title_full_unstemmed Neural cell 3D microtissue formation is marked by cytokines' up-regulation.
title_sort neural cell 3d microtissue formation is marked by cytokines' up-regulation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Cells cultured in three dimensional (3D) scaffolds as opposed to traditional two-dimensional (2D) substrates have been considered more physiologically relevant based on their superior ability to emulate the in vivo environment. Combined with stem cell technology, 3D cell cultures can provide a promising alternative for use in cell-based assays or biosensors in non-clinical drug discovery studies. To advance 3D culture technology, a case has been made for identifying and validating three-dimensionality biomarkers. With this goal in mind, we conducted a transcriptomic expression comparison among neural progenitor cells cultured on 2D substrates, 3D porous polystyrene scaffolds, and as 3D neurospheres (in vivo surrogate). Up-regulation of cytokines as a group in 3D and neurospheres was observed. A group of 13 cytokines were commonly up-regulated in cells cultured in polystyrene scaffolds and neurospheres, suggesting potential for any or a combination from this list to serve as three-dimensionality biomarkers. These results are supportive of further cytokine identification and validation studies with cells from non-neural tissue.
url http://europepmc.org/articles/PMC3203927?pdf=render
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AT kecheng neuralcell3dmicrotissueformationismarkedbycytokinesupregulation
AT williamskisaalita neuralcell3dmicrotissueformationismarkedbycytokinesupregulation
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