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Smooth muscle cell adhesion on crosslinked hyaluronan gels
Anand Ramamurthi1, Ivan Vesely
1Department of Biomedical Engineering, ND20, Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio 44120, USA.
Journal of Biomedical Materials Research
|February 9, 2002
Summary
Surface modifications to hyaluronic acid (HA)-based polymers (hylans) significantly improve cell attachment and proliferation. Texturizing hylan scaffolds and coating them with matrix factors enhances their potential as bioengineered materials.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Polymer Chemistry
Background:
- Hyaluronic acid (HA)-based polymers (hylans) offer excellent biocompatibility and tunable mechanical properties.
- Hylans can be structurally modified for use as cellular scaffolds.
Purpose of the Study:
- To evaluate divinyl sulfone-crosslinked solid and particulate hylans as cellular scaffolds.
- To investigate the impact of surface topography and matrix factor coating on cell behavior on hylan scaffolds.
Main Methods:
- Neonatal rat aortic smooth muscle cells were cultured on solid and particulate hylan gels.
- Hylan gels were coated with collagen I, ECM gel, laminin, and fibronectin, or left uncoated.
- Cell attachment, morphology, and proliferation were assessed over 4 weeks.
Main Results:
- Cell attachment was sparse on uncoated hylans but significantly enhanced on matrix factor-coated gels.
- Cell morphology varied based on matrix factors and hylan surface topography (solid vs. particulate).
- Particulate hylan surfaces promoted greater protein deposition, cell attachment, and proliferation, especially when coated with ECM gel.
Conclusions:
- Surface texturizing and matrix factor coating enhance cell attachment and proliferation on hylan scaffolds.
- Tailoring hylan surface characteristics is crucial for developing effective cell-hylan composite biomaterials.
- These findings support the development of advanced bioengineered materials for regenerative medicine.