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Fig. 1 | Cell Communication and Signaling

Fig. 1

From: Potential role of autophagy induced by FLT3-ITD and acid ceramidase in acute myeloid leukemia chemo-resistance: new insights

Fig. 1

Sphingolipid metabolism in a summary. Ceramide is a key component of sphingolipid metabolism. Ceramide is made from the condensation of serine and palmitoyl-CoA in the endoplasmatic reticulum (ER) by serine palmitoyltransferase (SPT). After further reduction and acylation by a ceramide synthase (CERS1-6), dihydrosphingosine (dHSph) is produced, which is then desaturated to generate ceramide. Ceramide can be altered to galactosylceramide (GalCer) in the ER, although most ceramide change occurs at the Golgi in a manner that is dependent on their following use. Ceramide is used in the Golgi to produce sphingomyelin (SM) and glycosphingolipids in processes mediated by sphingomyelin synthase 1 (SMS1) and glycosphingolipid synthases (GCSs). SM and glycosphingolipids are delivered to the plasma membrane from the Golgi. By the actions of secretory and neutral sphingomyelinases, SM can be converted back to ceramide (sSMase and nSMase). Ceramide can then be converted to ceramide-1-phosphate (C1P), sphingosine-1-phosphate (S1P), or SM. By accessing the endolysosomal process, complex sphingolipids in the membrane can be utilized as a pool for ceramide recycling. Acid SMases (aSMase) and glycosidases (GCase) create ceramide, which can then be hydrolyzed into sphingosine and utilized in ceramide production or degraded by phosphorylation into S1P followed by degradation to hexadecenal and ethanolamine-1-phosphate (EA1P). Ceramide kinase (CERK) can phosphorylate ceramide in the Golgi, resulting in ceramide-1-phosphate (C1P)

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