CER can be generated intracellularly via the de novo and recycling pathways. In the de novo pathway, palmitoyl-CoA and serine are converted to CER, a step catalyzed by serine palmitoyl transferase. In the recycling pathway, CER is formed via degradation of sphingomyelins; these steps are mediated by a variety of sphingomyelinases. CER is converted sphingosine by ceramidase. Sphingosine is converted to sphingosine-1-phosphate by sphingosine kinase. It is noteworthy that both CER and sphingosine have been shown to promote cell cycle arrest and cell senescence and induce cell apoptosis. Interestingly, however, sphingosine-1-phosphate exerts positive modulatory effects on cell function including cell proliferation, motility and survival. Therefore, intermediates of these pathway play both positive and negative modulatory roles in cell function.