The alternative complement pathway (ACP) in vertebrates is known to be
important in inflammatory reactions, and to be activated by foreign s
ubstances such as bacterial lipopolysaccharide (LPS) and zymosan. alth
ough to date no intrinsic activators have been identified except compl
ement receptor type 2. From the point of the structural similarity of
LPS to ganglioside, we have investigated gangliosides which are abunda
ntly present in animal cells for their activity on the human ACP. All
of seven gangliosides tested were found to activate this pathway in a
manner depending on the number of sialic acids and neutral sugars cont
ained in the molecules. A dose - response study suggested a correlatio
n of the threshold in ganglioside concentration with its critical mice
lle concentration. Gangliosides may thus serve as an intrinsic activat
or for ACP in animals, thereby leading to inflammation. The possibilit
y of the participation of sialidase in complement activation is also d
iscussed.