An imprint-based approach to replicate nano- to microscale roughness on gelatin hydrogel scaffolds: surface characterization and effect on endothelialization.
Ali SalehiStefanie SprejzHolger RuehlMonilola A OlayioyeGiorgio CattaneoPublished in: Journal of biomaterials science. Polymer edition (2024)
Biologization of biomaterials with endothelial cells (ECs) is an important step in vascular tissue engineering, aiming at improving hemocompatibility and diminishing the thrombo-inflammatory response of implants. Since subcellular topography in the scale of nano to micrometers can influence cellular adhesion, proliferation, and differentiation, we here investigate the effect of surface roughness on the endothelialization of gelatin hydrogel scaffolds. Considering the micron and sub-micron features of the different native tissues underlying the endothelium in the body, we carried out a biomimetic approach to replicate the surface roughness of tissues and analyzed how this impacted the adhesion and proliferation of human umbilical endothelial cells (HUVECs). Using an imprinting technique, nano and micro-roughness ranging from Sa= 402 nm to Sa= 8 μm were replicated on the surface of gelatin hydrogels. Fluorescent imaging of HUVECs on consecutive days after seeding revealed that microscale topographies negatively affect cell spreading and proliferation. By contrast, nanoscale roughnesses of Sa= 402 and Sa= 538 nm promoted endothelialization as evidenced by the formation of confluent cell monolayers with prominent VE-cadherin surface expression. Collectively, we present an affordable and flexible imprinting method to replicate surface characteristics of tissues on hydrogels and demonstrate how nanoscale roughness positively supports their endothelialization.
Keyphrases
- tissue engineering
- endothelial cells
- inflammatory response
- single cell
- hyaluronic acid
- gene expression
- signaling pathway
- drug delivery
- nitric oxide
- magnetic resonance
- poor prognosis
- stem cells
- atomic force microscopy
- high resolution
- quantum dots
- pseudomonas aeruginosa
- cell migration
- biofilm formation
- long non coding rna
- toll like receptor
- candida albicans
- high speed
- bone marrow
- contrast enhanced