Galectin-1 (Gal-1), a member of a family of beta-galactoside-binding protei
ns, has been suggested to play key roles in immunological and inflammatory
processes. The present study deals with the concept of an in vivo role for
Gal-1 in acute inflammation by using the rat hind paw edema test. Local adm
inistration of Gal-1 (0.5, 2, 4 and 8 mu g/ml) inhibited acute inflammation
induced by bee Venom phospholipase A(2) (PLA(2)) when it was injected 30 m
in before the enzyme or co-injected together with PLA,. The anti-inflammato
ry effect was prevented by a specific antibody, but independent of its carb
ohydrate-binding properties. In contrast, Gal-1 failed to inhibit histamine
-induced edema. Histopathological studies showed a clear reduction of the i
nflammatory process when Gal-1 was injected before PLA(2), evidenced by a d
iminished number of infiltrated polymorphonuclear neutrophils and scarce de
granulated mast cells. The anti-inflammatory effect was also assessed in vi
tro, showing that Gal-1 treatment reduced prostaglandin E-2 secretion and a
rachidonic acid release from stimulated peritoneal macrophages. Results pre
sented here provide the first evidence for a role of Gal-1 in acute inflamm
ation and suggest that the anti-inflammatory effect involves the inhibition
of both soluble and cellular mediators of the inflammatory response.