Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 286, Issue 32, Pages 27855-27862Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.R111.254359
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Funding
- National Institutes of Health [R01AG016583, R01GM062887]
- NCI [R01GM43825, R01GM63265, P01CA097132]
- Office of Research and Development, Department of Veterans Affairs
- Ralph H. Johnson Veterans Affairs Medical Center (Charleston, SC)
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Intensive research over the past 2 decades has implicated ceramide in the regulation of several cell responses. However, emerging evidence points to dramatic complexities in ceramide metabolism and structure that defy the prevailing unifying hypothesis on ceramide function that is based on the understanding of ceramide as a single entity. Here, we develop the concept that ceramide constitutes a family of closely related molecules, subject to metabolism by >28 enzymes and with >200 structurally distinct mammalian ceramides distinguished by specific structural modifications. These ceramides are synthesized in a combinatorial fashion with distinct enzymes responsible for the specific modifications. These multiple pathways of ceramide generation led to the hypothesis that individual ceramide molecular species are regulated by specific biochemical pathways in distinct subcellular compartments and execute distinct functions. In this minireview, we describe the many ceramides paradigm, along with the rationale, supporting evidence, and implications for our understanding of bioactive sphingolipids and approaches for unraveling these pathways.
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