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Perfusion culture enhanced human endometrial stromal cell growth in alginate‐multivalent integrin α5β1 ligand scaffolds
Author(s) -
Li Zhaohui,
Kreiner Michaela,
EdradaEbel RuAngelie,
Cui Zhanfeng,
van der Walle Christopher F.,
Mardon Helen J.
Publication year - 2011
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.33177
Subject(s) - extracellular matrix , fibronectin , stromal cell , materials science , scaffold , tissue engineering , cell culture , cell adhesion , integrin , biomedical engineering , perfusion , adhesion , biophysics , cell growth , microbiology and biotechnology , cell , chemistry , biology , biochemistry , cancer research , medicine , genetics , composite material
A method to functionalize alginate by introducing monomeric or self‐assembling (tetrameric) fibronectin (FN) domains is described, leading to a functional scaffold, which is used for three dimensional (3D) culture of human endometrial stromal cells (EnSCs). EnSCs encapsulated in the functional alginate were cultured under perfusion using the TissueFlex® platform, a multiple parallel microbioreactor system for 3D cell culture. The effect of the novel scaffold and the effect of perfusion were examined. Cell viability, proliferation, and extracellular matrix (ECM) deposition were determined and the results compared with those obtained with cells encapsulated in non‐functionalized alginate, and also those without perfusion. Staining for focal adhesions and actin showed maximal cell adhesion only for alginate‐tetrameric FN scaffolds under perfusion, associated with a significant increase in cell number over 7 days culture; in contrast to poor cell adhesion and a decrease in cell number for non‐functionalized alginate scaffolds (irrespective of perfused/static culture) and 3D static culture (irrespective of the scaffold). Conjugation of alginate to FN was an absolute requirement to attenuate the loss of cell metabolic activity over 7 days culture. ECM deposition for blank alginate and alginate‐monomeric FN was similar, but increased around 2‐fold and 3‐fold for alginate‐tetrameric FN under static and perfusion culture, respectively. It is concluded that the requirement for EnSC engagement with multivalent integrin α5β1 ligands and perfused culture are both essential as a first step toward endometrial tissue engineering. © 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part A:, 2011.