Effect of tuned elasticity and chemical modification of substrate on fibrotic and healthy lung fibroblasts

Abstract

Response to substrate elasticity, dependent on mechanical properties of cells, differs for lung fibroblast derived from idiopathic pulmonary fibrosis (IPF) and the healthy ones. These altered interactions might potentially act as a 'biomarker' for easy and reliable IPF diagnosis. In this work, systematic studies on the effect of polydimethylsiloxane (PDMS) substrate elasticity, tuned stepwise from 600 kPa to 1.5 MPa on the growth of IPF-derived (LL97A) and healthy (LL24) lung fibroblasts were reported. Additionally, impact of substrate chemistry on both cell lines was studied for fibroblasts cultured on glass substrates modified with three organosilanes - 3-aminopropyltriethoxysilane (APTES), 3-mercaptopropyltriethoxysilane (MPTES) and 3-glycidyloxypropyl trimethoxysilane (GOPS), with different end groups. Finally, the effect of the simultaneous modification of mechanical and chemical properties on the cellular behavior was studied for fibroblast cultured on PDMS substrates covered with silanes. The growth of cells was traced using fluorescence microscopy and analyzed quantitatively by nucleus-cytoplasm ratio, indicating strong, cell-dependent impact of substrate elasticity dominating over effect of chemical modification.

Keywords: Chemical modification; Idiopathic pulmonary fibrosis; Substrate elasticity.