The Journal of Cell Biology · 2021 · 173 citations · 41 references
Life SciencesCell BiologyMolecular BiologyLipid BiochemistryMolecular VirologyVirologyEndomembrane SystemLipid HomeostasisLipid MetabolismMembrane Lipid CompositionProtein-lipid InteractionsViral InfectionsCellular Cholesterol HomeostasisEndoplasmic Reticulum Lipid CompositionIntegral Membrane ProteinsLipid Droplet ProteinsOrganelle Biogenesis PathwaysPhospholipid ContentPhospholipid ScramblasesPhospholipid Scrambling
TMEM41B and VMP1 are integral membrane proteins of the endoplasmic reticulum (ER) and regulate the formation of autophagosomes, lipid droplets (LDs), and lipoproteins. Recently, TMEM41B was identified as a crucial host factor for infection by all coronaviruses and flaviviruses. The molecular function of TMEM41B and VMP1, which belong to a large evolutionarily conserved family, remains elusive. Here, we show that TMEM41B and VMP1 are phospholipid scramblases whose deficiency impairs the normal cellular distribution of cholesterol and phosphatidylserine. Their mechanism of action on LD formation is likely to be different from that of seipin. Their role in maintaining cellular phosphatidylserine and cholesterol homeostasis may partially explain their requirement for viral infection. Our results suggest that the proper sorting and distribution of cellular lipids are essential for organelle biogenesis and viral infection.
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