The ubiquitous sphingophospholipid sphingomyelin (SM) can be hydrolysed in
human cells to ceramide by different sphingomyelinases (SMases). These enzy
mes exert a dual role, enabling not only the turnover of membrane SM and th
e degradation of exogenous (lipoprotein) SM, but also the signal-induced ge
neration of the lipid second messenger ceramide. This review focuses on the
function(s) of the different SMases in living cells. While both lysosomal
and non-lysosomal pathways that ensure SM hydrolysis in intact cells can be
distinguished, the precise contribution of each of these SM-cleaving enzym
es to the production of ceramide as a signalling molecule remains to be cla
rified. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.