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Journal of Lipid Research
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    • Research Article6

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    • Anto, Liya1
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    • complementary DNA6
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    • Research Article
      Open Access

      Genetic dissection in mice reveals a dynamic crosstalk between the delivery pathways of vitamin A

      Journal of Lipid Research
      Vol. 63Issue 6100215Published online: April 19, 2022
      • Jean Moon
      • Srinivasagan Ramkumar
      • Johannes von Lintig
      Cited in Scopus: 3
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        Vitamin A is distributed within the body to support chromophore synthesis in the eyes and retinoid signaling in most other tissues. Two pathways exist for the delivery of vitamin A: the extrinsic pathway transports dietary vitamin A in lipoproteins from intestinal enterocytes to tissues, while the intrinsic pathway distributes vitamin A from hepatic stores bound to serum retinol binding protein (RBP). Previously, the intestine-specific homeodomain transcription factor (ISX) and the RBP receptor STRA6 were identified as gatekeepers of these pathways; however, it is not clear how mutations in the corresponding genes affect retinoid homeostasis.
        Genetic dissection in mice reveals a dynamic crosstalk between the delivery pathways of vitamin A
      • Research Article
        Open Access

        Hormone-sensitive lipase is localized at synapses and is necessary for normal memory functioning in mice

        Journal of Lipid Research
        Vol. 63Issue 5100195Published online: March 14, 2022
        • Cecilia Skoug
        • Cecilia Holm
        • João M.N. Duarte
        Cited in Scopus: 3
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          Hormone-sensitive lipase (HSL) is mainly present in adipose tissue where it hydrolyzes diacylglycerol. Although expression of HSL has also been reported in the brain, its presence in different cellular compartments is uncertain, and its role in regulating brain lipid metabolism remains hitherto unexplored. We hypothesized that HSL might play a role in regulating the availability of bioactive lipids necessary for neuronal function and therefore investigated whether dampening HSL activity could lead to brain dysfunction.
          Hormone-sensitive lipase is localized at synapses and is necessary for normal memory functioning in mice
        • Research Article
          Open Access

          Gut microbiome-derived glycine lipids are diet-dependent modulators of hepatic injury and atherosclerosis

          Journal of Lipid Research
          Vol. 63Issue 4100192Published online: March 9, 2022
          • Courtney L. Millar
          • Liya Anto
          • Chelsea Garcia
          • Mi-Bo Kim
          • Anisha Jain
          • Anthony A. Provatas
          • and others
          Cited in Scopus: 1
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            Oral and gut Bacteroidetes produce unique classes of serine-glycine lipodipeptides and glycine aminolipids that signal through host Toll-like receptor 2. These glycine lipids have also been detected in human arteries, but their effects on atherosclerosis are unknown. Here, we sought to investigate the bioactivity of bacterial glycine lipids in mouse models of atherosclerosis. Lipid 654 (L654), a serine-glycine lipodipeptide species, was first tested in a high-fat diet (HFD)-fed Ldlr−/− model of atherosclerosis.
            Gut microbiome-derived glycine lipids are diet-dependent modulators of hepatic injury and atherosclerosis
          • Research Article
            Open Access

            KIAA1363 affects retinyl ester turnover in cultured murine and human hepatic stellate cells

            Journal of Lipid Research
            Vol. 63Issue 3100173Published online: January 28, 2022
            • Carina Wagner
            • Victoria Hois
            • Annalena Eggeling
            • Lisa-Maria Pusch
            • Laura Pajed
            • Patrick Starlinger
            • and others
            Cited in Scopus: 3
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              Large quantities of vitamin A are stored as retinyl esters (REs) in specialized liver cells, the hepatic stellate cells (HSCs). To date, the enzymes controlling RE degradation in HSCs are poorly understood. In this study, we identified KIAA1363 (also annotated as arylacetamide deacetylase 1 or neutral cholesterol ester hydrolase 1) as a novel RE hydrolase. We show that KIAA1363 is expressed in the liver, mainly in HSCs, and exhibits RE hydrolase activity at neutral pH. Accordingly, addition of the KIAA1363-specific inhibitor JW480 largely reduced RE hydrolase activity in lysates of cultured murine and human HSCs.
              KIAA1363 affects retinyl ester turnover in cultured murine and human hepatic stellate cells
            • Research Article
              Open Access

              Elevated granulocyte-colony stimulating factor and hematopoietic stem cell mobilization in Niemann-Pick type C1 disease

              Journal of Lipid Research
              Vol. 63Issue 2100167Published online: January 7, 2022
              • Anouk G. Groenen
              • Anouk M. La Rose
              • Mengying Li
              • Venetia Bazioti
              • Arthur F. Svendsen
              • Niels J. Kloosterhuis
              • and others
              Cited in Scopus: 0
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                Niemann-Pick type C1 (NPC1) disease is a progressive lysosomal storage disorder caused by mutations of the NPC1 gene. While neurodegeneration is the most severe symptom, a large proportion of NPC1 patients also present with splenomegaly, which has been attributed to cholesterol and glycosphingolipid accumulation in late endosomes and lysosomes. However, recent data also reveal an increase in the inflammatory monocyte subset in the Npc1nih mouse model expressing an Npc1 null allele. We evaluated the contribution of hematopoietic cells to splenomegaly in NPC1 disease under conditions of hypercholesterolemia.
                Elevated granulocyte-colony stimulating factor and hematopoietic stem cell mobilization in Niemann-Pick type C1 disease
              • Research Article
                Open Access

                Loss of ABCA8B decreases myelination by reducing oligodendrocyte precursor cells in mice

                Journal of Lipid Research
                Vol. 63Issue 1100147Published online: November 6, 2021
                • Yiran Liu
                • David Castano
                • Francesco Girolamo
                • Laia Trigueros-Motos
                • Han-Gyu Bae
                • Suat Peng Neo
                • and others
                Cited in Scopus: 1
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                  The myelin sheath, which is wrapped around axons, is a lipid-enriched structure produced by mature oligodendrocytes. Disruption of the myelin sheath is observed in several neurological diseases, such as multiple sclerosis. A crucial component of myelin is sphingomyelin, levels of which can be increased by ABCA8, a member of the ATP-binding cassette transporter family. ABCA8 is highly expressed in the cerebellum, specifically in oligodendroglia. However, whether ABCA8 plays a role in myelination and mechanisms that would underlie this role remain unknown.
                  Loss of ABCA8B decreases myelination by reducing oligodendrocyte precursor cells in mice
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