Endothelial cells (EC) that form the inner lining of blood vessels remain q
uiescent in the normal adult vasculature except during angiogenesis and ree
ndothelialization, which result in EC proliferation and migration. EC place
d in culture at subconfluent density also undergo cell multiplication and m
ovement. This report demonstrates that whereas in confluent EC in a compact
monolayer, the EC-EC adhesion molecule platelet-endothelial cell adhesion
molecule-1 (PECAM-1) is strongly expressed at cell borders, little or no PE
CAM-1 immunostaining Is detected in sparse or migrating cultured EC. Consis
tent with this observation, steady-state PECAM-1 mRNA expression was much l
ower in subconfluent EC than in confluent EC. The absence of PECAM-1 expres
sion in sparse EC appeared not to be linked to ability to proliferate, sinc
e PECAM-1 expression remained low even in the presence of nitric oxide (NO)
or mitomycin C, agents that inhibit EC growth. However, another growth-inh
ibitory agent, TGF-beta1, did not alter PECAM-1 staining. Based on these ob
servations, it is hypothesized that cell-associated mechanical forces under
lying cell tensegrity regulate PECAM-1 expression.