Expression of E-selectin on activated endothelium is a critical initial ste
p that leads to extravasation of leucocytes during inflammation, yet E-sele
ctin is largely uncharacterized in several animal species including the hor
se. We have sequenced and compared E-selectin genes derived from activated
cultures of purified equine (horse), cervid (black-tailed deer) and ovine (
sheep) pulmonary artery endothelial cells (ECs). Phylogenetic and amino aci
d sequence comparisons indicate that bovine, cervid and ovine E-selectin ar
e similar, whereas human and equine E-selectin are more closely related to
each other than to the ruminant molecules. Human E- and P-selectin-specific
monoclonal antibodies that also recognize equine E-selectin were identifie
d and used to characterize its expression. Expression of E-selectin was mor
e readily induced by lipopolysaccharide treatment in equine ECs than in hum
an ECs and supported adhesion and activation of neutrophils, consistent wit
h the extreme sensitivity of horses to endotoxaemia and septic shock.