Literature DB >> 12190865

Human epidermal glucosylceramides are major precursors of stratum corneum ceramides.

Sumiko Hamanaka1, Mariko Hara, Hiroyuki Nishio, Fujio Otsuka, Akemi Suzuki, Yoshikazu Uchida.   

Abstract

Ceramides are the major component of the stratum corneum, accounting for 30%-40% of stratum corneum lipids by weight, and are composed of at least seven molecular groups (designated ceramides 1-7). Stratum corneum ceramides, together with cholesterol and fatty acids, form extracellular lamellae that are responsible for the epidermal permeability barrier. Previous studies indicated that beta-glucocerebrosidase- and sphingomyelinase-dependent ceramide production from glucosylceramides and sphingomyelins, respectively, is important for epidermal permeability barrier homeostasis. A recent study indicated that sphingomyelins are precursors of two stratum corneum ceramide molecular groups (ceramides 2 and 5). In this study, we have examined the role of glucosylceramides in the generation of each of the seven stratum corneum ceramide molecular groups. First, the structures of various glucosylceramide species in human epidermis were determined by gas chromatography-mass spectrometry, fast atom bombardment-mass spectrometry, and nuclear magnetic resonance. The results indicate that total epidermal glucosylceramides are composed of six distinct molecular groups, glucosylceramides 1-6. Glucosylceramide 1 contains sphingenine and nonhydroxy fatty acids, glucosylceramide 2, phytosphingosine and nonhydroxy fatty acids, glucosylceramide 3, phytosphingosine with one double bond and nonhydroxy fatty acids, glucosylceramide 4, sphingenine and alpha-hydroxy fatty acids, glucosylceramide 5, phytosphingosine and alpha-hydroxy fatty acids, and glucosylceramide 6, phytosphingosine with one double bond and alpha-hydroxy fatty acids. The nonhydroxy fatty acids typically have 16-24-carbon-length chains, whereas alpha-hydroxy fatty acids are limited to 24-, 25-, and 26-carbon chains. The sphingosine bases are C18 or C20 chains. Next, acylglucosylceramides and glucosylceramides were treated with beta-glucocerebrosidase and the ceramides released were compared with stratum corneum ceramides. Ceramide moieties of acylglucosylceramides and glucosylceramides 1, 2, 4-6 correspond to stratum corneum ceramides 1-7. These results, together with those of our previous reports characterizing epidermal sphingomyelins, indicate that all ceramide species, including omega-hydroxy fatty-acid-containing ceramides, are derived from glucosylceramides, and fractions of ceramides 2 and 5 are from sphingomyelins. Furthermore, structural analysis of glucosylceramides revealed that human epidermal glycosphingolipids display a unique lipid profile that is rich in very long chain hydroxylated (alpha- and omega-hydroxy) fatty acids and phytosphingosine.

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Year:  2002        PMID: 12190865     DOI: 10.1046/j.1523-1747.2002.01836.x

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  41 in total

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Journal:  Hum Mol Genet       Date:  2007-01-05       Impact factor: 6.150

2.  Vitamin D receptor and coactivators SRC2 and 3 regulate epidermis-specific sphingolipid production and permeability barrier formation.

Authors:  Yuko Oda; Yoshikazu Uchida; Sam Moradian; Debra Crumrine; Peter M Elias; Daniel D Bikle
Journal:  J Invest Dermatol       Date:  2008-12-04       Impact factor: 8.551

3.  Sphingolipids Modulate Secretion of Glycosylphosphatidylinositol-Anchored Plasmodesmata Proteins and Callose Deposition.

Authors:  Arya Bagus Boedi Iswanto; Jong Cheol Shon; Kwang Hyeon Liu; Minh Huy Vu; Ritesh Kumar; Jae-Yean Kim
Journal:  Plant Physiol       Date:  2020-07-07       Impact factor: 8.340

4.  Lowered humidity produces human epidermal equivalents with enhanced barrier properties.

Authors:  Richard Sun; Anna Celli; Debra Crumrine; Melanie Hupe; Lillian C Adame; Sally D Pennypacker; Kyungho Park; Yoshikazu Uchida; Kenneth R Feingold; Peter M Elias; Dusko Ilic; Theodora M Mauro
Journal:  Tissue Eng Part C Methods       Date:  2015-01       Impact factor: 3.056

5.  Gromwell (Lithospermum erythrorhizon) supplementation enhances epidermal levels of ceramides, glucosylceramides, β-glucocerebrosidase, and acidic sphingomyelinase in NC/Nga mice.

Authors:  Jungmin Kim; Yunhi Cho
Journal:  J Med Food       Date:  2013-09-27       Impact factor: 2.786

6.  Premature terminal differentiation and a reduction in specific proteases associated with loss of ABCA12 in Harlequin ichthyosis.

Authors:  Anna C Thomas; Daniel Tattersall; Elizabeth E Norgett; Edel A O'Toole; David P Kelsell
Journal:  Am J Pathol       Date:  2009-01-29       Impact factor: 4.307

7.  Elovl4 and Fa2h expression during rat spermatogenesis: a link to the very-long-chain PUFAs typical of germ cell sphingolipids.

Authors:  Florencia X Santiago Valtierra; Daniel A Peñalva; Jessica M Luquez; Natalia E Furland; Claudia Vásquez; Juan G Reyes; Marta I Aveldaño; Gerardo M Oresti
Journal:  J Lipid Res       Date:  2018-05-03       Impact factor: 5.922

8.  Endogenous β-glucocerebrosidase activity in Abca12⁻/⁻epidermis elevates ceramide levels after topical lipid application but does not restore barrier function.

Authors:  Jorge F Haller; Paul Cavallaro; Nicholas J Hernandez; Lee Dolat; Stephanie J Soscia; Ruth Welti; Gregory A Grabowski; Michael L Fitzgerald; Mason W Freeman
Journal:  J Lipid Res       Date:  2013-11-30       Impact factor: 5.922

9.  2,3,7,8-Tetrachlorodibenzo-p-dioxin-mediated production of reactive oxygen species is an essential step in the mechanism of action to accelerate human keratinocyte differentiation.

Authors:  Lawrence H Kennedy; Carrie Hayes Sutter; Sandra Leon Carrion; Quynh T Tran; Sridevi Bodreddigari; Elizabeth Kensicki; Robert P Mohney; Thomas R Sutter
Journal:  Toxicol Sci       Date:  2012-11-14       Impact factor: 4.849

10.  DES2 protein is responsible for phytoceramide biosynthesis in the mouse small intestine.

Authors:  Fumio Omae; Masao Miyazaki; Ayako Enomoto; Minoru Suzuki; Yusuke Suzuki; Akemi Suzuki
Journal:  Biochem J       Date:  2004-05-01       Impact factor: 3.857

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