The proliferation of human umbilical vein endothelial cells (HUVECs) cocult
ivated with live B. henselae was enhanced in a bacterial dose-dependent man
ner, and the stimulatory effect was specific to vascular endothelial cells.
The inactivation of B. henselae by UV or heat treatment abolished its stim
ulatory activity, suggesting that live bacteria is necessary for the growth
stimulation effect. To investigate the role of direct contact, live B. hen
selae were separated from HUVECs by a filter membrane (Millicell-CM insert)
. Even under this condition, an enhanced proliferation of HUVECs was observ
ed. However, no morphological changes in the HUVECs were apparent compared
to the B. henselae-infected cells. Furthermore, we isolated a nonpiliated s
train of B. henselae that is unable to attach to and enter into endothelial
cells. The nonpiliated strain possessed the ability to stimulate the proli
feration of cocultivated HUVECs the same as the piliated strain. Moreover,
the culture supernatants of B. henselae were also able to induce HUVEC prol
iferation. Our results indicate that the stimulation of HUVEC proliferation
by B. henselae is mediated by soluble factor(s) secreted from the bacteria
. (C) 1999 Academic Press.