Vanessa Christine Smith, Whitney Ann Ponwith, Steve Smith, Tugba Ozdemir
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引用次数: 0
Abstract
Purpose: The goal of this study was to evaluate the impact of hyaluronic acid binding peptide (HABP) on pericellular matrix remodeling and to determine whether this effect differs between adult and neonatal fibroblasts. Neonatal wound healing is characterized by minimal scarring compared to adult healing, which typically results in fibrotic scar formation. Hyaluronic acid (HA) plays an important role in extracellular matrix organization and collagen remodeling during scarless healing. We hypothesized that HABP would promote endogenous HA retention around the pericellular matrix and influence collagen remodeling in fibroblasts.
Methods: Adult and neonatal human dermal fibroblasts were cultured in both two-dimensional and three-dimensional environments. HABP-tethered surfaces were used to promote HA retention around cells. Pericellular matrix formation and cell morphology were assessed in two-dimensional culture, while collagen contraction and collagen fibril morphology were evaluated in three-dimensional collagen gel systems.
Results: Adult fibroblasts cultured on HABP surfaces appeared similar in shape to neonatal fibroblasts, suggesting that HABP could promote a more regenerative phenotype. Collagen contraction was steeper in peptide-tethered conditions than in control samples for both cell types. The presence of HABP increased contraction significantly in the presence of Hyaluronidase (HAdase). Collagen fibers exhibited altered width and organization in the presence of HABP and Scr-HABP compared with control samples.
Conclusions: These findings suggest that HABP enhances HA retention and alters collagen remodeling, supporting a pro-regenerative fibroblast remodeling response.
期刊介绍:
The field of cellular and molecular bioengineering seeks to understand, so that we may ultimately control, the mechanical, chemical, and electrical processes of the cell. A key challenge in improving human health is to understand how cellular behavior arises from molecular-level interactions. CMBE, an official journal of the Biomedical Engineering Society, publishes original research and review papers in the following seven general areas:
Molecular: DNA-protein/RNA-protein interactions, protein folding and function, protein-protein and receptor-ligand interactions, lipids, polysaccharides, molecular motors, and the biophysics of macromolecules that function as therapeutics or engineered matrices, for example.
Cellular: Studies of how cells sense physicochemical events surrounding and within cells, and how cells transduce these events into biological responses. Specific cell processes of interest include cell growth, differentiation, migration, signal transduction, protein secretion and transport, gene expression and regulation, and cell-matrix interactions.
Mechanobiology: The mechanical properties of cells and biomolecules, cellular/molecular force generation and adhesion, the response of cells to their mechanical microenvironment, and mechanotransduction in response to various physical forces such as fluid shear stress.
Nanomedicine: The engineering of nanoparticles for advanced drug delivery and molecular imaging applications, with particular focus on the interaction of such particles with living cells. Also, the application of nanostructured materials to control the behavior of cells and biomolecules.