Decreased Ceramide Transport Protein (CERT) Function Alters Sphingomyelin Production following UVB Irradiation
| Autor: | Miyuki Kawano, Alexandra Charruyer, Bruce A. Macher, Sean M. Bell, Kentaro Hanada, Ten-Yang Yen, Yoshikazu Uchida, Keigo Kumagai, Walter M. Holleran, Sounthala Douangpanya |
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| Rok vydání: | 2008 |
| Předmět: |
Keratinocytes
Ceramide Ultraviolet Rays Ceramide binding Apoptosis Lipids and Lipoproteins: Metabolism Regulation and Signaling Protein Serine-Threonine Kinases Nitric Oxide Transfection Models Biological Biochemistry Mice chemistry.chemical_compound Cell Line Tumor Sphingomyelin synthase Animals Humans Molecular Biology integumentary system biology Cell Biology Ceramide transport Sphingomyelins Cell biology Oxidative Stress HaCaT chemistry Cell culture biology.protein Sphingomyelin Dimerization HeLa Cells |
| Zdroj: | Journal of Biological Chemistry. 283:16682-16692 |
| ISSN: | 0021-9258 |
| Popis: | Increased cellular ceramide accounts in part for UVB irradiation-induced apoptosis in cultured human keratinocytes with concurrent increased glucosylceramide but not sphingomyelin generation in these cells. Given that conversion of ceramide to non-apoptotic metabolites such as sphingomyelin and glucosylceramide protects cells from ceramide-induced apoptosis, we hypothesized that failed up-regulation of sphingomyelin generation contributes to ceramide accumulation following UVB irradiation. Because both sphingomyelin synthase and glucosylceramide synthase activities were significantly decreased in UVB-irradiated keratinocytes, we investigated whether alteration(s) in the function of ceramide transport protein (or CERT) required for sphingomyelin synthesis occur(s) in UVB-irradiated cells. Fluorescently labeled N-(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-pentanoyl)-d-erythro-sphingosine (C(5)-DMB-ceramide) relocation to the Golgi was diminished after irradiation, consistent with decreased CERT function, whereas the CERT inhibitor N-(3-hydroxy-1-hydroxymethyl-3-phenylpropyl)dodecanamide (1R,3R isomer) (HPA-12) produced an equivalent effect. UVB irradiation also induced the rapid formation of a stable CERT homotrimer complex in keratinocytes as determined by Western immunoblot and mass spectrometry analyses, a finding replicated in HeLa, HEK293T, and HaCaT cells and in murine epidermis. Ceramide binding activity was decreased in recombinant CERT proteins containing the UVB-induced homotrimer. The middle region domain of the CERT protein was required for the homotrimer formation, whereas neither the pleckstrin homology (Golgi-binding) nor the START (ceramide-binding) domains were involved. Finally like UVB-treated keratinocytes, HPA-12 blockade of CERT function increased keratinocyte apoptosis, decreased sphingomyelin synthesis, and led to accumulation of ceramide. Thus, UVB-induced CERT homotrimer formation accounts, at least in part, for apoptosis and failed up-regulation of sphingomyelin synthesis following UVB irradiation, revealing that inactive CERT can attenuate a key metabolic protective mechanism against ceramide-induced apoptosis in keratinocytes. |
| Databáze: | OpenAIRE |
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