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Vol. 286, Issue 1, 439-446, July 1998
Department of Pathology, University of Michigan Medical School, Ann
Arbor, Michigan
We examined the protective effects of GM2941, a sulfated glycomimetic
of the complex carbohydrate sialyl Lewisx, in a model of
pulmonary granuloma development. This study was based on the rationale
that formation of glucan-induced lung granulomas is dependent on
neutrophils and that sialyl Lewisx glycomimetic (GM2941)
interferes, in vitro, with P-selectin-dependent neutrophil-endothelial adhesive interactions. Infusion of particulate yeast cell wall glucan into rats results in the rapid (48 hr) formation
of monocyte/macrophage-rich angiocentric pulmonary granulomas. Development of granulomas exhibits a temporal pattern characterized by
the early, transient influx of neutrophils into blood vessel walls at
sites of glucan embolization, followed by accumulation of monocytes and
macrophages that constitute the definitive angiocentric lesions. Within
1 hr after the infusion of glucan, immunohistochemical analysis
revealed up-regulation of blood vessel wall-associated P-selectin.
Previous studies utilizing neutrophil-depleted animals have revealed
that neutrophils, although not present in definitive lesions, are
required for full granuloma development. The potential of GM2941 to
inhibit neutrophil-endothelial cell adhesive interactions was
demonstrated by the ability of the compound to inhibit
P-selectin-mediated adhesion to histamine-stimulated HUVECs. Infusion
of GM2941 retarded pulmonary granuloma development in a dose-dependent
manner. Whole-lung myeloperoxidase activity, measured at the time of
peak neutrophil accumulation, was significantly reduced in animals
pretreated with GM2941 (30 mg/kg, 24 µM/kg), which suggests that this
compound affords protection, at least in part, through impedance of
neutrophil recruitment. These data indicate that GM2941 affords a
significant degree of protection against granuloma formation associated
with glucan infusion, probably through the interruption of neutrophil recruitment.