J. Lipid Res.
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Journal of Lipid Research, Vol. 41, 2071-2082, December 2000
Copyright © 2000 by Lipid Research, Inc.


Original Article

Epidermal sphingomyelins are precursors for selected stratum corneum ceramides

Yoshikazu Uchidaa,c, Mariko Harac, Hiroyuki Nishiod, Ellen Sidranskye, Shintaro Inouec, Fujio Otsukaf, Akemi Suzukig, Peter M. Eliasa, Walter M. Hollerana,b, and Sumiko Hamanakag
a Departments of Dermatology, University of California, San Francisco, CA 94143 and Dermatology Service and Research Unit, Department of Veterans Affairs Medical Center, San Francisco, CA 94121
b Pharmaceutical Chemistry, University of California, San Francisco, CA 94143 and Dermatology Service and Research Unit, Department of Veterans Affairs Medical Center, San Francisco, CA 94121
c Basic Research Laboratory, Kanebo Ltd., Odawara, 250-0002 Japan
d Cosmetics Laboratory, Kanebo Ltd., Odawara, 250-0002 Japan
e Section on Molecular Neurogenetics, National Institute of Mental Health, Bethesda, MD 20892
f Department of Dermatology, University of Tsukuba, Tsukuba, 305-0006 Japan
g RIKEN Frontier Research System, Suprabiomolecular System Research Group, Sphingolipid Expression Laboratory, Wako 351-0198, Japan

Correspondence to: Walter M. Holleran

Epidermal ceramides (Cer) comprise a heterogeneous family of seven species, including two unique {omega}-hydroxylated Cer, that are key components of the stratum corneum (SC) intercellular lamellar membranes responsible for the epidermal permeability barrier. Although both glucosylceramide (GlcCer) and the phospho-sphingolipid sphingomyelin (SM) are potential precursors of SC Cer, based on reported chemical structures of epidermal GlcCer and SC Cer, it is assumed that all major subfractions of SC Cer are generated from lamellar body-derived GlcCer. Yet, we and others have shown that SM-derived Cer are required for normal barrier homeostasis. Moreover, two pools of SM, one from plasma membrane, the other from lamellar body-derived contents, are potentially available for Cer production. To clarify the role of SM as a potential precursor of bulk or specific SC Cer, we compared Cer moieties in epidermal SM, Cer generated from epidermal SM by sphingomyelinase treatment, Cer within SC, and Cer that persist in Gaucher SC, where GlcCer cannot generate Cer due to an absence of ß-glucocerebrosidase. Using gas chromatography-mass spectrometry, fast atom bombardment-mass spectrometry, and nuclear magnetic resonance for Cer characterization, epidermal SM comprise three major subfractions with distinctive amide-linked (N-acyl) fatty acid (FA) compositions: that is, either long-chain FA (SM-1; C22;–26), short-chain FA (SM-2; primarily C16), and short-chain {alpha}-hydroxy FA (SM-3; C16;–18). In contrast, only trace quantities of {omega}-hydroxy FA were present. For each SM subfraction, the sphingoid base was either sphingosine or sphinganine, but phytosphingosine was not detected. Comparison of these SM with corresponding sphingomyelinase-generated epidermal Cer and SC Cer revealed that the Cer moieties of SM-1 and SM-3 are equivalent to Cer 2 (NS) and Cer 5 (AS), respectively. Moreover, both Cer 2 and Cer 5 occurred in Gaucher SC, whereas other Cer subfractions did not occur.

These results indicate that two epidermal SM, that is, SM-1 and SM-3, are important precursors of two corresponding Cer in mammalian SC, that is, Cer 2 and Cer 5, but other Cer species, including the {omega}-hydroxy Cer species, do not derive from SM. Uchida, Y., M. Hara, H. Nishio, E. Sidransky, S. Inoue, F. Otsuka, A. Suzuki, P. M. Elias, W. M. Holleran, and S. Hamanaka. Epidermal sphingomyelins are precursors for selected stratum corneum ceramides. J. Lipid Res. 2000. 41: 2071;–2082.

Supplementary key words: glucosylceramide, epidermis, Gaucher disease


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