S. Furuya et al., LYSOSPHINGOMYELIN-ELICITED CA2-BRAIN MICROSOMES( MOBILIZATION FROM RAT), Journal of lipid mediators and cell signalling, 14(1-3), 1996, pp. 303-311
We have examined the Ca2+ release activity of sphingolipid-derivatives
from rat brain microsomes using a Fura-2 cytofluorometric assay. Sphi
ngosylphosphorylcholine, lysosphingomyelin, elicited a rapid Ca2+ rele
ase from both cerebral and cerebellar microsomes. Other compounds incl
uding sphingosine and sphingosine-1-phosphate were incapable of causin
g the Ca2+. release. The pharmacological properties suggest that the s
phingosylphosphorylcholine-elicited Ca2+ mobilization is not mediated
by inositol 1,4,5-triphosphate receptors. Immunocytochemical study sho
w ed the occurrence of sphingomyelin, a putative precursor for sphingo
sylphosphorylcholine, in the somatodendritic membrane domains of cereb
ellar neurons. These observations imply that sphingosylphosphorylcholi
ne is a potent Ca2+ releaser in brain neurons.