Pathogenic variants of sphingomyelin synthase SMS2 disrupt lipid landscapes in the secretory pathway

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https://doi.org/10.48693/293
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Titel: Pathogenic variants of sphingomyelin synthase SMS2 disrupt lipid landscapes in the secretory pathway
Autor(en): Sokoya, Tolulope
Parolek, Jan
Foged, Mads Møller
Danylchuk, Dmytro I.
Bozan, Manuel
Sarkar, Bingshati
Hilderink, Angelika
Philippi, Michael
Botto, Lorenzo D.
Terhal, Paulien A.
Mäkitie, Outi
Piehler, Jacob
Kim, Yeongho
Burd, Christopher G.
Klymchenko, Andrey S.
Maeda, Kenji
Holthuis, Joost C. M.
ORCID des Autors: https://orcid.org/0000-0003-1831-8706
https://orcid.org/0000-0001-8912-1586
https://orcid.org/0000-0001-8426-369X
https://orcid.org/0000-0002-4547-001X
https://orcid.org/0000-0002-2143-2270
https://orcid.org/0000-0002-1477-925X
Zusammenfassung: Sphingomyelin is a dominant sphingolipid in mammalian cells. Its production in the trans-Golgi traps cholesterol synthesized in the ER to promote formation of a sphingomyelin/sterol gradient along the secretory pathway. This gradient marks a fundamental transition in physical membrane properties that help specify organelle identify and function. We previously identified mutations in sphingomyelin synthase SMS2 that cause osteoporosis and skeletal dysplasia. Here, we show that SMS2 variants linked to the most severe bone phenotypes retain full enzymatic activity but fail to leave the ER owing to a defective autonomous ER export signal. Cells harboring pathogenic SMS2 variants accumulate sphingomyelin in the ER and display a disrupted transbilayer sphingomyelin asymmetry. These aberrant sphingomyelin distributions also occur in patient-derived fibroblasts and are accompanied by imbalances in cholesterol organization, glycerophospholipid profiles, and lipid order in the secretory pathway. We postulate that pathogenic SMS2 variants undermine the capacity of osteogenic cells to uphold nonrandom lipid distributions that are critical for their bone forming activity.
Bibliografische Angaben: Tolulope Sokoya, Jan Parolek, Mads Møller Foged, Dmytro I Danylchuk, Manuel Bozan, Bingshati Sarkar, Angelika Hilderink, Michael Philippi, Lorenzo D Botto, Paulien A Terhal, Outi Mäkitie, Jacob Piehler, Yeongho Kim, Christopher G Burd, Andrey S Klymchenko, Kenji Maeda, Joost CM Holthuis (2022) Pathogenic variants of sphingomyelin synthase SMS2 disrupt lipid landscapes in the secretory pathway eLife 11:e79278
URL: https://doi.org/10.48693/293
https://osnadocs.ub.uni-osnabrueck.de/handle/ds-202304198687
Schlagworte: sphingolipid; mammalian cells; Sphingomyelin synthase
Erscheinungsdatum: 14-Sep-2022
Lizenzbezeichnung: Attribution 4.0 International
URL der Lizenz: http://creativecommons.org/licenses/by/4.0/
Publikationstyp: Einzelbeitrag in einer wissenschaftlichen Zeitschrift [Article]
Enthalten in den Sammlungen:FB05 - Hochschulschriften
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