1. Formation of keto-type ceramides in palmoplantar keratoderma based on biallelic KDSR mutations in patients
- Author
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Judith Fischer, Adam Majcher, Roger Sandhoff, Elise Brischoux-Boucher, Alexander Enk, Silvia Mihalceanu, Elisabeth Grimm, Knut Schäkel, Anne-Claire Bursztejn, François Aubin, Lukáš Opálka, Lionel Van Maldergem, and Robert Pilz
- Subjects
Ceramide ,Anabolism ,Reductase ,Biology ,Ceramides ,Compound heterozygosity ,Dermatitis, Atopic ,chemistry.chemical_compound ,Keratoderma, Palmoplantar ,Genetics ,medicine ,Stratum corneum ,Humans ,Molecular Biology ,Genetics (clinical) ,Sphingolipids ,Ichthyosis ,General Medicine ,Harlequin Ichthyosis ,medicine.disease ,Sphingolipid ,Molecular biology ,Palmoplantar keratoderma ,medicine.anatomical_structure ,chemistry ,Mutation ,Epidermis ,Oxidoreductases - Abstract
Functional skin barrier requires sphingolipid homeostasis; 3-ketodihydrosphingosine reductase or KDSR is a key enzyme of sphingolipid anabolism catalyzing the reduction of 3-ketodihydrosphingosine to sphinganine. Biallelic mutations in the KDSR gene may cause erythrokeratoderma variabilis et progressive-4, later specified as PERIOPTER syndrome, emphasizing a characteristic periorifical and ptychotropic erythrokeratoderma. We report another patient with compound heterozygous mutations in KDSR, born with generalized harlequin ichthyosis, which progressed into palmoplantar keratoderma. To determine whether patient-associated KDSR mutations lead to KDSR substrate accumulation and/or unrecognized sphingolipid downstream products in stratum corneum (SC), we analyzed lipids of this and previously published patients with non-identical biallelic mutations in KDSR. In SC of both patients, we identified ‘hitherto’ unobserved skin ceramides with an unusual keto-type sphingoid base in lesional and non-lesional areas, which accounted for up to 10% of the measured ceramide species. Furthermore, an overall shorter mean chain length of free and bound sphingoid bases was observed—shorter mean chain length of free sphingoid bases was also observed in lesional psoriasis vulgaris SC, but not generally in lesional atopic dermatitis SC. Formation of keto-type ceramides is probably due to a bottle neck in metabolic flux through KDSR and a bypass by ceramide synthases, which highlights the importance of tight intermediate regulation during sphingolipid anabolism and reveals substrate deprivation as potential therapy.
- Published
- 2021