A. Nathan et al., TISSUE ENGINEERED PERIVASCULAR ENDOTHELIAL-CELL IMPLANTS REGULATE VASCULAR INJURY, Proceedings of the National Academy of Sciences of the United Statesof America, 92(18), 1995, pp. 8130-8134
Molecular biomaterial engineering permits in vivo transplantation of c
ells and tissues, offering the promise of restoration of physiologic c
ontrol rather than pharmacologic dosing with isolated compounds, We en
grafted endothelial cells on Gelfoam biopolymeric matrices with retent
ion of viability, normal growth kinetics, immunoreactivity, and bioche
mical activity, The production of heparan sulfate proteoglycan and inh
ibition of basic fibroblast growth factor binding and activity by engr
afted cells were indistinguishable from endothelial cells grown in cul
ture, Perivascular implantation of Gelfoam-endothelial cell scaffolds
around balloon-denuded rat carotid arteries reduced intimal hyperplasi
a 88.1%, far better than the isolated administration of heparin, the m
ost effective endothelial mimic compound, In concert with a reduction
in intimal area, cell proliferation was reduced by > 90%. To our knowl
edge, there have been no previous reports of extravascular cell implan
ts controlling vasculoproliferative disease. Tissue engineered cells o
ffer the potential for potent methods of vascular growth regulation an
d insight into the complex autocrine-paracrine control mechanisms with
in the blood vessel wall.