We introduce two methods, both of which are based on cellular-extracel
lular matrix interaction, which will facilitate the study of human mic
rovascular endothelial cells. One method describes the means to obtain
a G1 population baseline in human microvasclular endothelial cells. B
ecause of the contribution of the extracellular matrix in endothelial
cell growth, synchronization in G1 was possible only after the incorpo
ration of angiostatic levels of heparin and hydrocortisone into the ex
tracellular matrix. In the second method, we demonstrate that selectiv
e perturbation of human microvascular endothelial cell-extracellular m
atrix interactions results in the induction of a transitional growth s
tate, between proliferative and differentiated growth states, in human
microvascular endothelial cells. In the functional, microtubule forma
tion assays, transitional growth state endothelial cells display rates
that are indermediate between those obtained from differentiated and
proliferative endothelial cells. Our results demonstrate the importanc
e of the human microvascular endothelial cell-extracellular matrix int
eraction in the determination of cellular growth state. Our findings a
lso imply that responsiveness of microvascular endothelial cells to th
eir cellular-extracellular matrix environs is highest during the diffe
rentiated growth state.