Heparin coated decellularized xenogeneic small diameter vascular conduit for vascular repair with early luminal reendothelialization.
Kishor R TardalkarTejas B MarsaleNilesh C BhamareJeevitaa R KshersagarJitendra K PatilArjun AdnaikMeghanad G JoshiPublished in: Cell and tissue banking (2022)
Small diameter vascular graft is a clinical need in cardiovascular disease (CAD) and peripheral atherosclerotic diseases (PAD). Autologous graft has limitations in availability and harvesting surgery. To make luminal surface modification with heparin coating in xenogeneic small diameter vascular graft. We constructed a conduit from decellularized human saphenous vein (HSV) matrices in small diameter vascular graft (< 0.8 mm diameter). Luminal surface modification was done with heparin coating for transplantation in the rat femoral artery. Biocompatibility of conduit was checked in Chorioallantoic Membrane (CAM) assay and in vivo. The blood flow rate in conduit grafts was measured, and immuno-histological analysis was performed. CAM assay and in vivo biocompatibility test showed cellular recruitment in the HSV scaffold. Heparin binding was achieved on the luminal surface. After three months of transplantation surgery neo-intimal layer was formed in the graft. The graft was patent for two weeks after surgery. There were no statistically differences between blood flow rate in graft (at proximal end 0.5 ± 0.01 m/s and at distal end 0.4 ± 0.01 m/s (n = 6)) and native artery (0.6 ± 0.1 m/second, (n = 3)). Biomarkers of endothelial cells, medial smooth muscle cells, and angiogenesis were observed in the transplanted graft. Our study demonstrates that xenogeneic decellularized vascular grafts with surface modification with heparin coating could be useful for the replacement of small diameter vessels.
Keyphrases
- blood flow
- endothelial cells
- venous thromboembolism
- cardiovascular disease
- optic nerve
- minimally invasive
- growth factor
- coronary artery bypass
- tissue engineering
- coronary artery disease
- stem cells
- extracellular matrix
- acute coronary syndrome
- percutaneous coronary intervention
- atrial fibrillation
- dna binding
- cardiovascular risk factors
- induced pluripotent stem cells