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Journal of Lipid Research
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    • Research Article10

    Author

    • Alvarez-Jarreta, Jorge1
    • Anto, Liya1
    • Arya, Arvind1
    • Balamir, Melek1
    • Bentley, Kirsten1
    • Blesso, Christopher N1
    • Boucher, Jeremie1
    • Brown, Richard William1
    • Buurma, Niklaas J1
    • Calabresi, Laura1
    • Chaurasia, Bhagirath1
    • Choi, Jungmin1
    • Chu, Catherine1
    • Clark, Robert B1
    • Couture, Patrick1
    • Cruz-López, Pio1
    • Dane, Adriaan D1
    • Deng, Mingjuan1
    • Dong, Weilai1
    • Garcia, Chelsea1
    • Geley, Stephan1
    • Golderer, Georg1
    • González, Jose Gerardo1
    • Griffiths, William J1
    • Hagstedt, Therese1

    Keyword

    • triglyceride9
    • CE3
    • lipidomics3
    • lipoproteins3
    • PC3
    • phosphatidylcholine3
    • triglycerides3
    • Cer2
    • ceramide2
    • HbA1c2
    • HFD2
    • IS2
    • PS2
    • TC2
    • (L)PC[O]/[P]1
    • (L)PE[O]/[P]1
    • 3-isobutyl-1-methylxanthine1
    • 3T3-L11
    • ACar1
    • ACE21
    • AE1
    • ALT1
    • ANGPTL41
    • ASCVD1

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    • Research Article
      Open Access

      Associations between insulin-like growth factor binding protein-2 and lipoprotein kinetics in men

      Journal of Lipid Research
      Vol. 63Issue 10100269Published online: August 28, 2022
      • Chloé Rauzier
      • Benoît Lamarche
      • André J. Tremblay
      • Patrick Couture
      • Frédéric Picard
      Cited in Scopus: 0
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        Low circulating concentrations of insulin-like growth factor binding protein-2 (IGFBP-2) have been associated with dyslipidemia, notably with high triglyceride (TG) levels. However, the determinants by which IGFBP-2 influences lipoprotein metabolism, especially that of TG-rich lipoproteins (TRLs), are poorly understood. Here, we aimed to assess the relationships between IGFBP-2 levels and lipoprotein production and catabolism in human subjects. Fasting IGFBP-2 concentrations were measured in the plasma of 219 men pooled from previous lipoprotein kinetics studies.
      • Research Article
        Open Access

        ANGPTL4 silencing via antisense oligonucleotides reduces plasma triglycerides and glucose in mice without causing lymphadenopathy

        Journal of Lipid Research
        Vol. 63Issue 7100237Published online: June 3, 2022
        • Mingjuan Deng
        • Elda Kutrolli
        • Anne Sadewasser
        • Sven Michel
        • Masoumeh Motamedi Joibari
        • Frank Jaschinski
        • and others
        Cited in Scopus: 1
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          Angiopoietin-like 4 (ANGPTL4) is an important regulator of plasma triglyceride (TG) levels and an attractive pharmacological target for lowering plasma lipids and reducing cardiovascular risk. Here, we aimed to study the efficacy and safety of silencing ANGPTL4 in the livers of mice using hepatocyte-targeting GalNAc-conjugated antisense oligonucleotides (ASOs). Compared with injections with negative control ASO, four injections of two different doses of ANGPTL4 ASO over 2 weeks markedly downregulated ANGPTL4 levels in liver and adipose tissue, which was associated with significantly higher adipose LPL activity and lower plasma TGs in fed and fasted mice, as well as lower plasma glucose levels in fed mice.
          ANGPTL4 silencing via antisense oligonucleotides reduces plasma triglycerides and glucose in mice without causing lymphadenopathy
        • Research Article
          Open Access

          Saroglitazar is noninferior to fenofibrate in reducing triglyceride levels in hypertriglyceridemic patients in a randomized clinical trial

          Journal of Lipid Research
          Vol. 63Issue 7100233Published online: May 20, 2022
          • Rene Rodriguez-Gutierrez
          • Jose Gerardo González
          • Deven Parmar
          • Farheen. Shaikh
          • Pio Cruz-López
          Cited in Scopus: 0
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            Saroglitazar, being a dual PPAR-α/γ agonist, has shown beneficial effect in diabetic dyslipidemia and hypertriglyceridemia. Fibrates are commonly used to treat severe hypertriglyceridemia. However, the effect of saroglitazar in patients with moderate to severe hypertriglyceridemia was not evaluated. We conducted a study to compare the efficacy and safety of saroglitazar (4 mg) with fenofibrate (160 mg) in patients with moderate to severe hypertriglyceridemia. This was a multicenter, randomized, double-blinded, double-dummy, active-control, and noninferiority trial in adult patients with fasting triglyceride (TG) levels of 500–1,500 mg/dl.
            Saroglitazar is noninferior to fenofibrate in reducing triglyceride levels in hypertriglyceridemic patients in a randomized clinical trial
          • Research Article
            Open Access

            Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans

            Journal of Lipid Research
            Vol. 63Issue 7100232Published online: May 18, 2022
            • Chiara Pavanello
            • Alice Ossoli
            • Arianna Strazzella
            • Patrizia Risè
            • Fabrizio Veglia
            • Marie Lhomme
            • and others
            Cited in Scopus: 0
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              Mutations in the LCAT gene cause familial LCAT deficiency (Online Mendelian Inheritance in Man ID: #245900), a very rare metabolic disorder. LCAT is the only enzyme able to esterify cholesterol in plasma, whereas sterol O-acyltransferases 1 and 2 are the enzymes esterifying cellular cholesterol in cells. Despite the complete lack of LCAT activity, patients with familial LCAT deficiency exhibit circulating cholesteryl esters (CEs) in apoB-containing lipoproteins. To analyze the origin of these CEs, we investigated 24 carriers of LCAT deficiency in this observational study.
              Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans
            • Research Article
              Open Access

              Adaptations of the 3T3-L1 adipocyte lipidome to defective ether lipid catabolism upon Agmo knockdown

              Journal of Lipid Research
              Vol. 63Issue 6100222Published online: May 7, 2022
              • Sabrina Sailer
              • Katharina Lackner
              • Mia L. Pras-Raves
              • Eric J.M. Wever
              • Jan B. van Klinken
              • Adriaan D. Dane
              • and others
              Cited in Scopus: 0
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                Little is known about the physiological role of alkylglycerol monooxygenase (AGMO), the only enzyme capable of cleaving the 1-O-alkyl ether bond of ether lipids. Expression and enzymatic activity of this enzyme can be detected in a variety of tissues including adipose tissue. This labile lipolytic membrane-bound protein uses tetrahydrobiopterin as a cofactor, and mice with reduced tetrahydrobiopterin levels have alterations in body fat distribution and blood lipid concentrations. In addition, manipulation of AGMO in macrophages led to significant changes in the cellular lipidome, and alkylglycerolipids, the preferred substrates of AGMO, were shown to accumulate in mature adipocytes.
                Adaptations of the 3T3-L1 adipocyte lipidome to defective ether lipid catabolism upon Agmo knockdown
              • Research Article
                Open Access

                Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia

                Journal of Lipid Research
                Vol. 63Issue 6100209Published online: April 20, 2022
                • Weilai Dong
                • Karen H.Y. Wong
                • Youbin Liu
                • Michal Levy-Sakin
                • Wei-Chien Hung
                • Mo Li
                • and others
                Cited in Scopus: 0
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                  Low levels of high density lipoprotein-cholesterol (HDL-C) are associated with an elevated risk of arteriosclerotic coronary heart disease. Heritability of HDL-C levels is high. In this research discovery study, we used whole-exome sequencing to identify damaging gene variants that may play significant roles in determining HDL-C levels. We studied 204 individuals with a mean HDL-C level of 27.8 ± 6.4 mg/dl (range: 4–36 mg/dl). Data were analyzed by statistical gene burden testing and by filtering against candidate gene lists.
                  Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia
                • Research Article
                  Open Access

                  The SARS-CoV2 envelope differs from host cells, exposes procoagulant lipids, and is disrupted in vivo by oral rinses

                  Journal of Lipid Research
                  Vol. 63Issue 6100208Published online: April 14, 2022
                  • Zack Saud
                  • Victoria J. Tyrrell
                  • Andreas Zaragkoulias
                  • Majd B. Protty
                  • Evelina Statkute
                  • Anzelika Rubina
                  • and others
                  Cited in Scopus: 9
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                    The lipid envelope of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an essential component of the virus; however, its molecular composition is undetermined. Addressing this knowledge gap could support the design of antiviral agents as well as further our understanding of viral-host protein interactions, infectivity, pathogenicity, and innate immune system clearance. Lipidomics revealed that the virus envelope comprised mainly phospholipids (PLs), with some cholesterol and sphingolipids, and with cholesterol/phospholipid ratio similar to lysosomes.
                    The SARS-CoV2 envelope differs from host cells, exposes procoagulant lipids, and is disrupted in vivo by oral rinses
                  • Research Article
                    Open Access

                    Determination of tissue contributions to the circulating lipid pool in cold exposure via systematic assessment of lipid profiles

                    Journal of Lipid Research
                    Vol. 63Issue 7100197Published online: March 14, 2022
                    • Raghav Jain
                    • Gina Wade
                    • Irene Ong
                    • Bhagirath Chaurasia
                    • Judith Simcox
                    Cited in Scopus: 1
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                      Plasma lipid levels are altered in chronic conditions such as type 2 diabetes and cardiovascular disease as well as during acute stresses such as fasting and cold exposure. Advances in MS-based lipidomics have uncovered a complex plasma lipidome of more than 500 lipids that serve functional roles, including as energy substrates and signaling molecules. This plasma lipid pool is maintained through regulation of tissue production, secretion, and uptake. A major challenge in understanding the lipidome complexity is establishing the tissues of origin and uptake for various plasma lipids, which is valuable for determining lipid functions.
                      Determination of tissue contributions to the circulating lipid pool in cold exposure via systematic assessment of lipid profiles
                    • 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

                        The SGLT2 inhibitor dapagliflozin promotes systemic FFA mobilization, enhances hepatic β-oxidation, and induces ketosis

                        Journal of Lipid Research
                        Vol. 63Issue 3100176Published online: February 1, 2022
                        • Kristina Wallenius
                        • Tobias Kroon
                        • Therese Hagstedt
                        • Lars Löfgren
                        • Maria Sörhede-Winzell
                        • Jeremie Boucher
                        • and others
                        Cited in Scopus: 15
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                          Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been shown to increase ketone bodies in patients with type 2 diabetes; however, the underlying mechanisms have not been fully elucidated. Here we examined the effect of the SGLT2 inhibitor dapagliflozin (1 mg/kg/day, formulated in a water, PEG400, ethanol, propylene glycol solution, 4 weeks) on lipid metabolism in obese Zucker rats. Fasting FFA metabolism was assessed in the anesthetized state using a [9,10-3H(N)]-palmitic acid tracer by estimating rates of plasma FFA appearance (Ra), whole-body FFA oxidation (Rox), and nonoxidative disposal (Rst).
                          The SGLT2 inhibitor dapagliflozin promotes systemic FFA mobilization, enhances hepatic β-oxidation, and induces ketosis
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