## Abstract Hyaluronan (HA) accumulates in vascular disease but its functional role is not fully understood. To investigate the impact of HA enriched extracellular matrices (ECM) on cell phenotype, arterial smooth muscle cells (ASMCs) were transduced with retroviral constructs (LXSN) encoding murin
Smooth muscle cell adhesion on crosslinked hyaluronan gels
✍ Scribed by Ramamurthi, Anand ;Vesely, Ivan
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 187 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0021-9304
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Hyaluronic acid (HA)‐based polymers (hylans) are highly biocompatible and can be structurally modified to obtain desired mechanical properties. This study evaluated divinyl sulfone‐crosslinked solid and particulate hylans as cellular scaffolds. These two hylan types differ in surface characteristics, mode of preparation, HA content, and extent of crosslinking. Neonatal rat aortic smooth muscle cells were cultured on hylan gels coated with matrix factors including collagen I, ECM gel, laminin, and fibronectin and on uncoated controls for ≤4 weeks. Cell attachment was sparse on uncoated controls but significantly enhanced on coated gels. Cell morphology was influenced by the identity of the matrix factors coated and the surface topography of the hylan gels. Cells attached to coated particulate gels appeared either highly spread (collagen, fibronectin) or irregularly shaped (ECM gel, laminin). Cells on laminin and fibronectin‐coated solid gels were rounded and nonproliferative. Cells proliferated most rapidly on ECM gel‐coated gels. The uneven surface of particulate gels induced more protein deposition and the subsequent attachment and active proliferation of cells. This study shows that surface texturizing and subsequent surface treatment with matrix factors enhances cell attachment and proliferation of hylans. These results are useful toward developing bioengineered materials based on cell‐hylan composites. © 2002 Wiley Periodicals, Inc. J Biomed Mater Res 60: 196–205, 2002
📜 SIMILAR VOLUMES
## Abstract Smooth muscle cells (SMC) were cultured for up to 6 days on copolymer films fabricated from a PCL‐PEG‐PCL block copolymer or P(ε‐CL‐__co__‐D,L‐LA)‐PEG‐P(ε‐CL‐__co__‐D,L‐LA), named P(100/0) and P(70/30), respectively. The films were modified by aminolysis using 1,6‐hexanediamine, and fib
## Abstract The effects of cell adhesion peptides (RGDS, KQAGDV, VAPG) on vascular smooth muscle cells grown on modified surfaces and in tissue‐engineering scaffolds were examined. Cells were more strongly adhered to surfaces modified with adhesive ligands than to control surfaces (no ligand or a n
## Abstract Previous studies investigating the design of synthetic bladder wall substitutes have involved polymers with micro dimensional structures. Since the body is made up of nano‐structured components (e.g., extracellular matrix proteins), the focus of the present __in vitro__ study was to des
## Abstract Smooth muscle cell migration, proliferation, and deposition of extracellular matrix are key events in atherogenesis and restenosis development. To explore the mechanisms that regulate smooth muscle cell function, we have investigated whether perlecan, a basement membrane heparan sulfate