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Phosphatidylserine decarboxylase is critical for the maintenance of skeletal muscle mitochondrial integrity and muscle mass.

Ahrathy Selathurai | Greg M Kowalski | Shaun A Mason | Damien L Callahan | Victoria C Foletta | Paul A Della Gatta | Angus Lindsay | Steven Hamley | Gunveen Kaur | Annie R Curtis | Micah L Burch | Teddy Ang | Sean L McGee | Clinton R Bruce
Molecular metabolism | 2019

Phosphatidylethanolamine (PtdEtn) is a major phospholipid in mammals. It is synthesized via two pathways, the CDP-ethanolamine pathway in the endoplasmic reticulum and the phosphatidylserine (PtdSer) decarboxylase (PSD) pathway in the mitochondria. While the CDP-ethanolamine pathway is considered the major route for PtdEtn synthesis in most mammalian tissues, little is known about the importance of the PSD pathway in vivo, especially in tissues enriched with mitochondria such as skeletal muscle. Therefore, we aimed to examine the role of the mitochondrial PSD pathway in regulating PtdEtn homeostasis in skeletal muscle in vivo.

Pubmed ID: 31285171

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