Published December 23, 2022 | Version v1

Dataset related to the article "LUMINAL ENDOTHELIALIZATION OF SMALL CALIBER SILK TUBULAR GRAFT FOR VASCULAR CONSTRUCTS ENGINEERING"

  • 1. Centro Cardiologico Monzino, IRCCS, Milan, Italy; Ph.D. Program in Biomedical Engineering, Politecnico di Milano, Milan, Italy
  • 2. Department of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, Milan, Italy
  • 3. Centro Cardiologico Monzino, IRCCS, Milan, Italy

Description

This record contains raw data related to the article “LUMINAL ENDOTHELIALIZATION OF SMALL CALIBER SILK TUBULAR GRAFT FOR VASCULAR CONSTRUCTS ENGINEERING"

The constantly increasing incidence of coronary artery disease worldwide makes necessary to set advanced therapies and tools such as tissue engineered vessel grafts (TEVGs) to surpass the autologous grafts [(i.e., mammary and internal thoracic arteries, saphenous vein (SV)] currently employed in coronary artery and vascular surgery. To this aim, in vitro cellularization of artificial tubular scaffolds still holds a good potential to overcome the unresolved problem of vessel conduits availability and the issues resulting from thrombosis, intima hyperplasia and matrix remodeling, occurring in autologous grafts especially with small caliber (<6 mm). The employment of silk-based tubular scaffolds has been proposed as a promising approach to engineer small caliber cellularized vascular constructs. The advantage of the silk material is the excellent manufacturability and the easiness of fiber deposition, mechanical properties, low immunogenicity and the extremely high in vivo biocompatibility. In the present work, we propose a method to optimize coverage of the luminal surface of silk electrospun tubular scaffold with endothelial cells. Our strategy is based on seeding endothelial cells (ECs) on the luminal surface of the scaffolds using a low-speed rolling. We show that this procedure allows the formation of a nearly complete EC monolayer suitable for flow-dependent studies and vascular maturation, as a step toward derivation of complete vascular constructs for transplantation and disease modeling.

Notes

This present work has been funded by the Institutional project grants at Centro Cardiologico Monzino (Ricerca Corrente; Progetto 5 per 1000), issued to MP.

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Is supplement to
Journal article: 10.3389/fcvm.2022.1013183 (DOI)