Premium
Dynamic culture induces a cell type‐dependent response impacting on the thickness of engineered connective tissues
Author(s) -
Fortier Guillaume Marceau,
Gauvin Robert,
Proulx Maryse,
Vallée Maud,
Fradette Julie
Publication year - 2013
Publication title -
journal of tissue engineering and regenerative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.835
H-Index - 72
eISSN - 1932-7005
pISSN - 1932-6254
DOI - 10.1002/term.522
Subject(s) - connective tissue , tissue engineering , biomedical engineering , microbiology and biotechnology , materials science , engineering , biology , genetics
Mesenchymal cells are central to connective tissue homeostasis and are widely used for tissue‐engineering applications. Dermal fibroblasts and adipose‐derived stromal cells (ASCs) allow successful tissue reconstruction by the self‐assembly approach of tissue engineering. This method leads to the production of multilayered tissues, devoid of exogenous biomaterials, that can be used as stromal compartments for skin or vesical reconstruction. These tissues are formed by combining cell sheets, generated through cell stimulation with ascorbic acid, which favours the cell‐derived production/organization of matrix components. Since media motion can impact on cell behaviour, we investigated the effect of dynamic culture on mesenchymal cells during tissue reconstruction, using the self‐assembly method. Tissues produced using ASCs in the presence of a wave‐like movement were nearly twice thicker than under standard conditions, while no difference was observed for tissues produced from dermal fibroblasts. The increased matrix deposition was not correlated with an increased proliferation of ASCs, or by higher transcript levels of fibronectin or collagens I and III. A 30% increase of type V collagen mRNA was observed. Interestingly, tissues engineered from dermal fibroblasts featured a four‐fold higher level of MMP‐1 transcripts under dynamic conditions. Mechanical properties were similar for tissues reconstructed using dynamic or static conditions. Finally, cell sheets produced using ASCs under dynamic conditions could readily be manipulated, resulting in a 2 week reduction of the production time (from 5 to 3 weeks). Our results describe a distinctive property of ASCs' response to media motion, indicating that their culture under dynamic conditions leads to optimized tissue engineering. Copyright © 2011 John Wiley & Sons, Ltd.