Abstract
Endothelial cells play a central role in the vascular system, where their function is tightly regulated by both cell-extracellular matrix (e.g., via integrins) and cell–cell interactions (e.g., via cadherins). In this study, we incorporated cholesterol-modified integrin and N-cadherin peptide binding ligands in fluid supported lipid bilayers. Human umbilical vein endothelial cell adhesion, spreading and vinculin localization in these cells were dependent on ligand density. One composition led to observe a higher extent of cell spreading, where cells exhibited extensive lamellipodia formation and a qualitatively more distinct N-cadherin localization at the cell periphery, which is indicative of N-cadherin clustering and a mimic of cell–cell contact formation. The results can be used to reconstitute the endothelial-pericyte interface on biomedical devices and materials.
| Original language | English |
|---|---|
| Article number | 116850 |
| Journal | Bioorganic & medicinal chemistry |
| Volume | 68 |
| Early online date | 25 May 2022 |
| DOIs | |
| Publication status | Published - 15 Aug 2022 |
Keywords
- Cell-instructive
- Cell-surface interactions
- Peptide ligands
- Supported lipid bilayers
- Surface modification
- UT-Hybrid-D
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