The use of poly(ethylene glycol) hydrogels to investigate the impact of ECM chemistry and mechanics on smooth muscle cells

Hydrogels based on poly(ethylene glycol) (PEG) are of increasing interest for regenerative medicine applications and are ideal materials to direct cell function due to the ability to confer key functionalities of native extracellular matrix (ECM) on PEG's otherwise inert backbone. Given extensi...

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Veröffentlicht in:Biomaterials 2006-10, Vol.27 (28), p.4881-4893
Hauptverfasser: Peyton, Shelly R., Raub, Christopher B., Keschrumrus, Vic P., Putnam, Andrew J.
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container_end_page 4893
container_issue 28
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container_title Biomaterials
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creator Peyton, Shelly R.
Raub, Christopher B.
Keschrumrus, Vic P.
Putnam, Andrew J.
description Hydrogels based on poly(ethylene glycol) (PEG) are of increasing interest for regenerative medicine applications and are ideal materials to direct cell function due to the ability to confer key functionalities of native extracellular matrix (ECM) on PEG's otherwise inert backbone. Given extensive recent evidence that ECM compliance influences a variety of cell functions, PEG-based hydrogels are also attractive due to the ease with which their mechanical properties can be controlled. In these studies, we exploited the chemical and mechanical tunability of PEG-based gels to study the impact of ECM chemistry and mechanics on smooth muscle cells (SMCs) in both 2-D and 3-D model systems. First, by controlling the extent of crosslinking and therefore the mechanical properties of PEG-based hydrogels (tensile moduli from 13.7 to 423.9 kPa), we report here that the assembly of F-actin stress fibers and focal adhesions, indicative of the state of actin contractility, were influenced by the compliance of 2-D PEG gels functionalized with either short adhesive peptides or full-length ECM proteins. Varying ECM ligand density and identity independent of gel compliance affected the physical properties of the focal adhesions, and also influenced SMC spreading in 2-D. Furthermore, SMCs proliferated to a greater extent as gel stiffness was increased. In contrast, the degree of SMC differentiation, which was qualitatively assessed by the extent of smooth muscle α-actin bundling and the association of calponin and caldesmon with the α-actin fibrils, was found to decrease with substrate stiffness in 2-D cultures. In 3-D, despite the fact that their viability and degree of spreading were greatly reduced, SMCs did express some contractile markers indicative of their differentiated phenotype when cultured within PEG–RGDS constructs. Combined, these data suggest that the mechanical and chemical properties of PEG hydrogels can be tuned to influence SMC phenotype in both 2-D and 3-D.
doi_str_mv 10.1016/j.biomaterials.2006.05.012
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Actins - analysis
Actins - metabolism
Cell Culture Techniques - methods
Cell Differentiation - drug effects
Cell Movement - drug effects
Cell proliferation
Cells, Cultured
Cytoskeleton - drug effects
Cytoskeleton - metabolism
ECM
Extracellular Matrix - chemistry
Focal Adhesions - drug effects
Humans
Hydrogel
Hydrogels
Mechanical properties
Microscopy, Confocal
Microscopy, Fluorescence
Myocytes, Smooth Muscle - chemistry
Myocytes, Smooth Muscle - cytology
Myocytes, Smooth Muscle - drug effects
Oligopeptides - chemistry
Oligopeptides - pharmacology
Polyethylene
Polyethylene Glycols - chemistry
Polyethylene Glycols - pharmacology
Smooth muscle cell
Stress, Mechanical
Tissue Engineering - methods
title The use of poly(ethylene glycol) hydrogels to investigate the impact of ECM chemistry and mechanics on smooth muscle cells
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