Hepatic C9 cells switch their behaviour in short or long exposure to soft substrates

• Published in: Biology of the cell 2020-10, Vol.112 (10), p.265-279
• Main Authors: Cabriales, Lucia, Hautefeuille, Mathieu, Vázquez‐Victorio, Genaro, Martinez‐Pastor, David, Carretero‐Ortega, Jorge, Jiménez‐Escobar, Alejandra, Macias‐Silva, Marina
• Format: Article
• Language: English
• Subjects: C9 hepatic cell line; Life Sciences; MAPK signalling; Polydimethylsiloxane; Proliferation regulation; Substrate stiffness
• ISSN: 0248-4900; 1768-322X
• DOI: 10.1111/boc.201900115

Background Information There have been several studies to understand the influence of stiffness of the culture substrates for different types of adherent cells. It is generally accepted that cell proliferation, spreading and focal adhesions increase with higher matrix stiffness. However, what remains unclear is whether this kind of cell behaviour may be reverted by culturing on soft substrates those cell lines that were originally selected or primed on stiff surfaces. Results Here, we studied the influence of substrate softness on proliferation, adhesion and morphology of the highly proliferative hepatic C9 cell line. We cultured C9 cells on soft and stiff polydimethylsiloxane (PDMS) substrates prepared with two different elastic moduli in the range of 10 and 200 kPa, respectively. Lower cell proliferation was observed on substrates with lower stiffness without affecting cell viability. The proliferation rate of C9 cell line along with extracellular growth‐regulated kinase (ERK) phosphorylation was decreased on soft PDMS. Despite this cell line has been described as a hepatic epithelial cell, our characterisation demonstrated that the origin of C9 cells is uncertain, although clearly epithelial, with the expression of markers of several hepatic cells. Surprisingly, consecutive passages of C9 cells on soft PDMS did not alter this mesenchymal phenotype, vimentin expression did not decrease when culturing cells in soft substrates, even though the ERK phosphorylation levels eventually were increased after several passages on soft PDMS, triggering again an increase of cell proliferation. Conclusions and Significance This study shows that the exposure of C9 cells to soft substrates promoted a decrease of cell proliferation rate, as reported for other types of cells on PDMS, whereas a much longer term exposure caused cells to adapt to softness after trained for several passages, reactivating proliferation. During this phenomenon, the morphology and phenotype of trained cells was modified accompanying the increase of cell proliferation rate contrary to the effect observed in short periods of cell culture. In contrast to previous reports, cell death was not observed during these experiments, discarding a cell selection mechanism and suggesting soft cell adaptation may be limited in time in C9 cells. Research article: The figure shows how cell proliferation is regulated by substrate softness in hepatic C9 cell line. The cell proliferation rate of C9 cells and their