eCM (Eur Cell Mater / e Cells & Materials) Not-for-profit Open Access
Created by Scientists, for Scientists
 ISSN:1473-2262         NLM:100973416 (link)         DOI:10.22203/eCM

2013   Volume No 25 – pages 97-113

Title: Computational model combined with in vitro experiments to analyse mechanotransduction during mesenchymal stem cell adhesion

Author: J-L Milan, S Lavenus, P Pilet, G Louarn, S Wendling, D Heymann, P Layrolle, P Chabrand

Address: Rensselaer Polytechnic Institute, Nanotechnology Center and CBIS,110 Eighth Street, MRC-210, Troy, NY 12180-3590, USA

E-mail: lavens at

Key Words: Mesenchymal stem cells; cell adhesion; cell morphology; computational cell adhesion model; cytoskeleton; mechanical forces; mechanotransduction.

Publication date: January 16th 2013

Abstract: The shape that stem cells reach at the end of adhesion process influences their differentiation. Rearrangement of cytoskeleton and modification of intracellular tension may activate mechanotransduction pathways controlling cell commitment. In the present study, the mechanical signals involved in cell adhesion were computed in in vitro stem cells of different shapes using a single cell model, the so-called Cytoskeleton Divided Medium (CDM) model. In the CDM model, the filamentous cytoskeleton and nucleoskeleton networks were represented as a mechanical system of multiple tensile and compressive interactions between the nodes of a divided medium. The results showed that intracellular tonus, focal adhesion forces as well as nuclear deformation increased with cell spreading. The cell model was also implemented to simulate the adhesion process of a cell that spreads on protein-coated substrate by emitting filopodia and creating new distant focal adhesion points. As a result, the cell model predicted cytoskeleton reorganisation and reinforcement during cell spreading. The present model quantitatively computed the evolution of certain elements of mechanotransduction and may be a powerful tool for understanding cell mechanobiology and designing biomaterials with specific surface properties to control cell adhesion and differentiation.

Article download: Pages 97-113 (PDF file)
DOI: 10.22203/eCM.v025a07

Supplementary files (avi): Video1