Objective: The ideal small-caliber arterial graft remains elusive despite s
everal decades of intense research. A novel approach to the development of
small-caliber arterial prostheses with a biomimetic system for in vitro ves
sel culture has recently been described. In this study we examined the effe
cts of culture time and tissue culture scaffolding on engineered vessel mor
phology and function and found that these parameters greatly influence the
function of engineered vessels.
Methods: This report describes the effects of culture time and scaffold typ
e on vessel morphology cellular differentiation, and vessel mechanical char
acteristics. Engineered vessels were cultured from bovine aortic smooth mus
cle cells (SMCs) and endothelial cells that were seeded onto biodegradable
polymer scaffolds and cultured under physiologically pulsatile conditions.
Engineered vessels were subjected to histologic, ultrastructural, immunocyt
ochemical, and mechanical analyses.
Results: Vessel morphology and mechanical characteristics improved as time
in culture increased to 8 weeks. SMCs in the engineered vessel wall were or
ganized into a highly lamellar structure, with cells separated by alternati
ng layers of collagen fibrils. Polymer scaffold remnants were present in ve
ssels cultured for 8 weeks, and SMCs that were in proximity to polymer renm
ants exhibited a dedifferentiated phenotype.
Conclusions: These findings aid in the systematic understandings of the eff
ects of in vitro parameters on engineered vessels and will be useful for th
e translation of vessel culture techniques to human cells for the developme
nt of autologous human vascular grafts.