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Growth Factor-Bearing Polymer Brushes--Versatile Bioactive Substrates Influencing Cell Response
Evmorfia Psarra1,2, Elena Foster3, Ulla König1
1Leibniz Institute of Polymer Research Dresden , Hohe Strasse 6, 01069 Dresden, Germany.
Biomacromolecules
|October 9, 2015
Summary
Responsive polymer brushes functionalized with growth factors (GFs) guide cell behavior. Chemisorption offers controlled release of hepatocyte growth factor (HGF) and basic fibroblast growth factor (bFGF), enhancing cell culture substrates.
Area of Science:
- Biomaterials Science
- Cell Biology
- Surface Chemistry
Background:
- Developing advanced cell culture substrates is crucial for regenerative medicine and biological research.
- Controlling cell behavior requires precise presentation of bioactive cues.
- Polymer brushes offer a versatile platform for surface modification and biomolecule immobilization.
Purpose of the Study:
- To develop responsive nanoscale substrates with cell-guiding properties using bioactive signaling cues.
- To investigate the effect of surface-bound hepatocyte growth factor (HGF) and basic fibroblast growth factor (bFGF) on cell behavior.
- To compare physisorption and chemisorption strategies for growth factor immobilization on poly(acrylic)acid (PAA) polymer brushes.
Main Methods:
- Fabrication of dense poly(acrylic)acid (PAA) polymer brush films.
- Biofunctionalization of PAA brushes with HGF and bFGF via physisorption and chemisorption.
- Characterization of growth factor release kinetics.
- Assessment of cell response (growth inhibition, scattering, differentiation) on modified substrates using HepG2 cells and mouse embryonic stem cells (mESCs).
Main Results:
- Both physisorption and chemisorption achieved high growth factor binding efficiencies.
- Physisorbed GFs showed an initial burst release, followed by slow release.
- Chemisorbed HGF exhibited sustained binding (>1 week), while chemisorbed bFGF showed slow release.
- GF-functionalized PAA brushes demonstrated measurable effects on HepG2 cell growth inhibition/scattering and mESC differentiation.
Conclusions:
- PAA polymer brushes can be effectively biofunctionalized with GFs using both physisorption and chemisorption.
- Chemisorption provides enhanced control over GF release kinetics and surface retention.
- GF-modified PAA brushes serve as versatile bioactive cell culture substrates with tunable efficiency for specific cell responses.

