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Mechanically and Chemically Tunable Cell Culture System for Studying the Myofibroblast Phenotype
Author(s) -
Michele K. Saums,
Wei-Feng Wang,
Biao Han,
Lakshmi Madhavan,
Lin Han,
Daeyeon Lee,
Rebecca G. Wells
Publication year - 2014
Publication title -
langmuir
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.042
H-Index - 333
eISSN - 1520-5827
pISSN - 0743-7463
DOI - 10.1021/la4047758
Subject(s) - lumican , self healing hydrogels , myofibroblast , hepatic stellate cell , matrix (chemical analysis) , extracellular matrix , biophysics , cell culture , nanotechnology , chemistry , materials science , microbiology and biotechnology , fibrosis , biochemistry , biology , proteoglycan , pathology , composite material , polymer chemistry , medicine , genetics , decorin
Cell culture systems for studying the combined effects of matrix proteins and mechanical forces on the behavior of soft tissue cells have not been well developed. Here, we describe a new biomimetic cell culture system that allows for the study of mixtures of matrix proteins while controlling mechanical stiffness in a range that is physiological for soft tissues. This system consists of layer-by-layer (LbL)-assembled films of native matrix proteins atop mechanically tunable soft supports. We used hepatic stellate cells, which differentiate to myofibroblasts in liver fibrosis, for proof-of-concept studies. By culturing cells on collagen and lumican LbL-modified hydrogels, we demonstrate that this system is noncytotoxic and offers a valid control substrate, that the hydrogel determines the overall system mechanics, and that the addition of lumican to collagen influences the stellate cell phenotype. LbL-modified hydrogels offer the potential to study the influence of complex environmental factors on soft-tissue cells in culture.

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