PROFILING EXTRACELLULAR MATRIX REMODELING IN AN IN VITRO FIBROBLAST AND EPITHELIAL CELL CO-CULTURE MODEL
Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal interstitial lung disease driven by persistent fibroblast activation, abnormal epithelial to mesenchymal signaling and excessive extracellular matrix (ECM) remodeling. Better pre-clinical models are needed to reproduce these processes and to support antifibrotic drug development. This thesis tested whether an in vitro co-culture model
