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Journal of Lipid Research
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    • Fong, Vincent2
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    Keyword

    • 7-DHC4
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    • 7-dehydrocholesterol3
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    • Research Article
      Open Access

      Individual and simultaneous treatment with antipsychotic aripiprazole and antidepressant trazodone inhibit sterol biosynthesis in the adult brain

      Journal of Lipid Research
      Vol. 63Issue 8100249Published online: July 12, 2022
      • Marta Balog
      • Allison Anderson
      • Thiago C. Genaro-Mattos
      • Zeljka Korade
      • Karoly Mirnics
      Cited in Scopus: 2
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        Polypharmacy, or the simultaneous use of multiple drugs to treat a single patient, is a common practice in psychiatry. Unfortunately, data on the health effects of commonly used combinations of medications are very limited. In this study, we therefore investigated the effects and interactions between two commonly prescribed psychotropic medications with sterol inhibiting side effects, trazodone (TRZ), an antidepressant, and aripiprazole (ARI), an antipsychotic. In vitro cell culture experiments revealed that both medications alone disrupted neuronal and astroglial sterol biosynthesis in dose-dependent manners.
        Individual and simultaneous treatment with antipsychotic aripiprazole and antidepressant trazodone inhibit sterol biosynthesis in the adult brain
      • Research Article
        Open Access

        The small GTPase RAB10 regulates endosomal recycling of the LDL receptor and transferrin receptor in hepatocytes

        Journal of Lipid Research
        Vol. 63Issue 8100248Published online: June 23, 2022
        • Taslima Gani Khan
        • David Ginsburg
        • Brian T. Emmer
        Cited in Scopus: 0
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          The low-density lipoprotein receptor (LDLR) mediates the hepatic uptake of circulating low-density lipoproteins (LDLs), a process that modulates the development of atherosclerotic cardiovascular disease. We recently identified RAB10, encoding a small GTPase, as a positive regulator of LDL uptake in hepatocellular carcinoma cells (HuH7) in a genome-wide CRISPR screen, though the underlying molecular mechanism for this effect was unknown. We now report that RAB10 regulates hepatocyte LDL uptake by promoting the recycling of endocytosed LDLR from RAB11-positive endosomes to the plasma membrane.
          The small GTPase RAB10 regulates endosomal recycling of the LDL receptor and transferrin receptor in hepatocytes
        • Research Article
          Open Access

          Measurement of 7-dehydrocholesterol and cholesterol in hair can be used in the diagnosis of Smith-Lemli-Opitz syndrome

          Journal of Lipid Research
          Vol. 63Issue 6100228Published online: May 13, 2022
          • Yitao Luo
          • Chengqiang Zhang
          • Li Ma
          • Yuxiao Zhang
          • Zhengyuan Liu
          • Li Chen
          • and others
          Cited in Scopus: 0
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            7-dehydrocholesterol (7-DHC) and cholesterol (CHOL) are biomarkers of Smith-Lemli-Opitz Syndrome (SLOS), a congenital autosomal recessive disorder characterized by elevated 7-DHC level in patients. Hair samples have been shown to have great diagnostic and research value, which has long been neglected in the SLOS field. In this study, we sought to investigate the feasibility of using hair for SLOS diagnosis. In the presence of antioxidants (2,6-ditert-butyl-4-methylphenol and triphenylphosphine), hair samples were completely pulverized and extracted by micro-pulverized extraction in alkaline solution or in n-hexane.
            Measurement of 7-dehydrocholesterol and cholesterol in hair can be used in the diagnosis of Smith-Lemli-Opitz syndrome
          • Research Article
            Open Access

            ω-O-Acylceramides but not ω-hydroxy ceramides are required for healthy lamellar phase architecture of skin barrier lipids

            Journal of Lipid Research
            Vol. 63Issue 6100226Published online: May 11, 2022
            • Lukáš Opálka
            • Jason M. Meyer
            • Veronika Ondrejčeková
            • Linda Svatošová
            • Franz P.W. Radner
            • Kateřina Vávrová
            Cited in Scopus: 3
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              Epidermal omega-O-acylceramides (ω-O-acylCers) are essential components of a competent skin barrier. These unusual sphingolipids with ultralong N-acyl chains contain linoleic acid esterified to the terminal hydroxyl of the N-acyl, the formation of which requires the transacylase activity of patatin-like phospholipase domain containing 1 (PNPLA1). In ichthyosis with dysfunctional PNPLA1, ω-O-acylCer levels are significantly decreased, and ω-hydroxylated Cers (ω-OHCers) accumulate. Here, we explore the role of the linoleate moiety in ω-O-acylCers in the assembly of the skin lipid barrier.
              ω-O-Acylceramides but not ω-hydroxy ceramides are required for healthy lamellar phase architecture of skin barrier lipids
            • Research Article
              Open Access

              Chronic cholesterol depletion increases F-actin levels and induces cytoskeletal reorganization via a dual mechanism

              Journal of Lipid Research
              Vol. 63Issue 5100206Published online: April 4, 2022
              • Parijat Sarkar
              • G. Aditya Kumar
              • Sandeep Shrivastava
              • Amitabha Chattopadhyay
              Cited in Scopus: 2
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                Previous work from us and others has suggested that cholesterol is an important lipid in the context of the organization of the actin cytoskeleton. However, reorganization of the actin cytoskeleton upon modulation of membrane cholesterol is rarely addressed in the literature. In this work, we explored the signaling crosstalk between cholesterol and the actin cytoskeleton by using a high-resolution confocal microscopic approach to quantitatively measure changes in F-actin content upon cholesterol depletion.
                Chronic cholesterol depletion increases F-actin levels and induces cytoskeletal reorganization via a dual mechanism
              • 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

                  Cholesterol sulfate fluidizes the sterol fraction of the stratum corneum lipid phase and increases its permeability

                  Journal of Lipid Research
                  Vol. 63Issue 3100177Published online: February 6, 2022
                  • Ferdinand Fandrei
                  • Oskar Engberg
                  • Lukáš Opálka
                  • Pavla Jančálková
                  • Petra Pullmannová
                  • Miloš Steinhart
                  • and others
                  Cited in Scopus: 0
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                    Desulfation of cholesterol sulfate (CholS) to cholesterol (Chol) is an important event in epidermal homeostasis and necessary for stratum corneum (SC) barrier function. The CholS/Chol ratio decreases during SC maturation but remains high in pathological conditions, such as X-linked ichthyosis, characterized by dry and scaly skin. The aim of this study was to characterize the influence of the CholS/Chol molar ratio on the structure, dynamics, and permeability of SC lipid model mixtures. We synthesized deuterated CholS and investigated lipid models with specifically deuterated components using 2H solid-state NMR spectroscopy at temperatures from 25°C to 80°C.
                    Cholesterol sulfate fluidizes the sterol fraction of the stratum corneum lipid phase and increases its permeability
                  • Research Article
                    Open Access

                    Generation and validation of a conditional knockout mouse model for desmosterolosis

                    Journal of Lipid Research
                    Vol. 62100028Published online: January 29, 2021
                    • Babunageswararao Kanuri
                    • Vincent Fong
                    • Sithara Raju Ponny
                    • Ranjuna Weerasekera
                    • Kirthi Pulakanti
                    • Kriya S. Patel
                    • and others
                    Cited in Scopus: 0
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                      The enzyme 3β-hydroxysterol-Δ24 reductase (DHCR24, EC 1.3.1.72) catalyzes the conversion of desmosterol to cholesterol and is obligatory for post-squalene cholesterol synthesis. Genetic loss of this enzyme results in desmosterolosis (MIM # 602398 ), a rare disease that presents with multiple congenital anomalies, features of which overlap with subjects with the Smith-Lemli-Opitz syndrome (another post-squalene cholesterol disorder). Global knockout (KO) of Dhcr24 in mice recapitulates the biochemical phenotype, but pups die within 24 h from a lethal dermopathy, limiting its utility as a disease model.
                      Generation and validation of a conditional knockout mouse model for desmosterolosis
                    • Research Article
                      Open Access

                      The ligand-bound state of a G protein-coupled receptor stabilizes the interaction of functional cholesterol molecules

                      Journal of Lipid Research
                      Vol. 62100059Published online: February 26, 2021
                      • Laura Lemel
                      • Katarzyna Nieścierowicz
                      • M. Dolores García-Fernández
                      • Leonardo Darré
                      • Thierry Durroux
                      • Marta Busnelli
                      • and others
                      Cited in Scopus: 0
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                        Cholesterol is a major component of mammalian plasma membranes that not only affects the physical properties of the lipid bilayer but also is the function of many membrane proteins including G protein-coupled receptors. The oxytocin receptor (OXTR) is involved in parturition and lactation of mammals and in their emotional and social behaviors. Cholesterol acts on OXTR as an allosteric modulator inducing a high-affinity state for orthosteric ligands through a molecular mechanism that has yet to be determined.
                        The ligand-bound state of a G protein-coupled receptor stabilizes the interaction of functional cholesterol molecules
                      • Research Article
                        Open Access

                        25-Hydroxycholesterol 3-sulfate is an endogenous ligand of DNA methyltransferases in hepatocytes

                        Journal of Lipid Research
                        Vol. 62100063Published online: March 7, 2021
                        • Yaping Wang
                        • Weiqi Lin
                        • James E. Brown
                        • Lanming Chen
                        • Williams M. Pandak
                        • Phillip B. Hylemon
                        • and others
                        Cited in Scopus: 0
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                          The oxysterol sulfate, 25-hydroxycholesterol 3-sulfate (25HC3S), has been shown to play an important role in lipid metabolism, inflammatory response, and cell survival. However, the mechanism(s) of its function in global regulation is unknown. The current study investigates the molecular mechanism by which 25HC3S functions as an endogenous epigenetic regulator. To study the effects of oxysterols/sterol sulfates on epigenetic modulators, 12 recombinant epigenetic enzymes were used to determine whether 25HC3S acts as their endogenous ligand.
                          25-Hydroxycholesterol 3-sulfate is an endogenous ligand of DNA methyltransferases in hepatocytes
                        • Research Article
                          Open Access

                          Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure

                          Journal of Lipid Research
                          Vol. 62100083Published online: April 30, 2021
                          • Hannah L.M. Steffen
                          • Josephine L.C. Anderson
                          • Margot L. Poot
                          • Yu Lei
                          • Margery A. Connelly
                          • Stephan J.L. Bakker
                          • and others
                          Cited in Scopus: 0
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                            Lipoprotein-proteoglycan binding is an early key event in atherosclerotic lesion formation and thus conceivably could play a major role in vasculopathy-driven chronic graft failure and cardiovascular mortality in renal transplant recipients. The present study investigated whether lipoprotein-proteoglycan binding susceptibility (LPBS) of apoB-containing lipoproteins and levels of the classical atherosclerosis biomarker LDL-C were associated with cardiovascular mortality (n = 130) and graft failure (n = 73) in 589 renal transplant recipients who were followed up from at least 1 year after transplantation for 9.5 years.
                            Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure
                          • Research Article
                            Open Access

                            Evaluation of the available cholesterol concentration in the inner leaflet of the plasma membrane of mammalian cells

                            Journal of Lipid Research
                            Vol. 62100084Published online: May 4, 2021
                            • Pawanthi Buwaneka
                            • Arthur Ralko
                            • Shu-Lin Liu
                            • Wonhwa Cho
                            Cited in Scopus: 0
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                              Cholesterol is an essential component of the mammalian plasma membrane involved in diverse cellular processes. Our recent quantitative imaging analysis using ratiometric cholesterol sensors showed that the available cholesterol concentration in the inner leaflet of the plasma membrane (IPM) is low in unstimulated cells and increased in a stimulus-specific manner to trigger cell signaling events. However, the transbilayer distribution of cholesterol in the plasma membrane of mammalian cells remains controversial.
                              Evaluation of the available cholesterol concentration in the inner leaflet of the plasma membrane of mammalian cells
                            • Research Article
                              Open Access

                              Monomeric bile acids modulate the ATPase activity of detergent-solubilized ABCB4/MDR3

                              Journal of Lipid Research
                              Vol. 62100087Published online: May 19, 2021
                              • Tim Kroll
                              • Sander H.J. Smits
                              • Lutz Schmitt
                              Cited in Scopus: 0
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                                ABCB4, also called multidrug-resistant protein 3 (MDR3), is an ATP binding cassette transporter located in the canalicular membrane of hepatocytes that specifically translocates phosphatidylcholine (PC) lipids from the cytoplasmic to the extracellular leaflet. Due to the harsh detergent effect of bile acids, PC lipids provided by ABCB4 are extracted into the bile. While it is well known that bile acids are the major extractor of PC lipids from the membrane into bile, it is unknown whether only PC lipid extraction is improved or whether bile acids also have a direct effect on ABCB4.
                                Monomeric bile acids modulate the ATPase activity of detergent-solubilized ABCB4/MDR3
                              • Research Article
                                Open Access

                                Shark liver oil supplementation enriches endogenous plasmalogens and reduces markers of dyslipidemia and inflammation

                                Journal of Lipid Research
                                Vol. 62100092Published online: June 15, 2021
                                • Sudip Paul
                                • Adam Alexander T. Smith
                                • Kevin Culham
                                • Kevin A. Gunawan
                                • Jacqueline M. Weir
                                • Michelle A. Cinel
                                • and others
                                Cited in Scopus: 0
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                                  Plasmalogens are membrane glycerophospholipids with diverse biological functions. Reduced plasmalogen levels have been observed in metabolic diseases; hence, increasing their levels might be beneficial in ameliorating these conditions. Shark liver oil (SLO) is a rich source of alkylglycerols that can be metabolized into plasmalogens. This study was designed to evaluate the impact of SLO supplementation on endogenous plasmalogen levels in individuals with features of metabolic disease. In this randomized, double-blind, placebo-controlled cross-over study, the participants (10 overweight or obese males) received 4-g Alkyrol® (purified SLO) or placebo (methylcellulose) per day for 3 weeks followed by a 3-week washout phase and were then crossed over to 3 weeks of the alternate placebo/Alkyrol® treatment.
                                  Shark liver oil supplementation enriches endogenous plasmalogens and reduces markers of dyslipidemia and inflammation
                                • Research Article
                                  Open Access

                                  Antisense oligonucleotide–mediated inhibition of angiopoietin-like protein 3 increases reverse cholesterol transport in mice

                                  Journal of Lipid Research
                                  Vol. 62100101Published online: August 5, 2021
                                  • Thomas A. Bell III
                                  • Mingxia Liu
                                  • Aaron J. Donner
                                  • Richard G. Lee
                                  • Adam E. Mullick
                                  • Rosanne M. Crooke
                                  Cited in Scopus: 0
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                                    Supported by an abundance of experimental and genetic evidence, angiopoietin-like protein 3 (ANGPTL3) has emerged as a promising therapeutic target for cardiovascular disease. ANGPTL3 is primarily produced by the liver and is a potent modulator of plasma lipids and lipoproteins. Experimental models and subjects with loss-of-function Angptl3 mutations typically present with lower levels of HDL-C than noncarriers. The effect of ANGPTL3 on HDL-C is typically attributed to its function as an inhibitor of the enzyme endothelial lipase.
                                    Antisense oligonucleotide–mediated inhibition of angiopoietin-like protein 3 increases reverse cholesterol transport in mice
                                  • Research Article
                                    Open Access

                                    Nonalcoholic fatty liver disease stratification by liver lipidomics

                                    Journal of Lipid Research
                                    Vol. 62100104Published online: August 9, 2021
                                    • Olga Vvedenskaya
                                    • Tim Daniel Rose
                                    • Oskar Knittelfelder
                                    • Alessandra Palladini
                                    • Judith Andrea Heidrun Wodke
                                    • Kai Schuhmann
                                    • and others
                                    Cited in Scopus: 18
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                                      Nonalcoholic fatty liver disease (NAFLD) is a common metabolic dysfunction leading to hepatic steatosis. However, NAFLD's global impact on the liver lipidome is poorly understood. Using high-resolution shotgun mass spectrometry, we quantified the molar abundance of 316 species from 22 major lipid classes in liver biopsies of 365 patients, including nonsteatotic patients with normal or excessive weight, patients diagnosed with NAFL (nonalcoholic fatty liver) or NASH (nonalcoholic steatohepatitis), and patients bearing common mutations of NAFLD-related protein factors.
                                      Nonalcoholic fatty liver disease stratification by liver lipidomics
                                    • Research Article
                                      Open Access

                                      HSP90 inhibitors reduce cholesterol storage in Niemann-Pick type C1 mutant fibroblasts

                                      Journal of Lipid Research
                                      Vol. 62100114Published online: September 2, 2021
                                      • Nina H. Pipalia
                                      • Syed Z. Saad
                                      • Kanagaraj Subramanian
                                      • Abigail Cross
                                      • Aisha al-Motawa
                                      • Kunal Garg
                                      • and others
                                      Cited in Scopus: 0
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                                        Niemann-Pick type C1 (NPC1) disease is a lysosomal lipid storage disorder caused by mutations of the NPC1 gene. More than 300 disease-associated mutations are reported in patients, resulting in abnormal accumulation of unesterified cholesterol, glycosphingolipids, and other lipids in late endosomes and lysosomes (LE/Ly) of many cell types. Previously, we showed that treatment of many different NPC1 mutant fibroblasts with histone deacetylase inhibitors resulted in reduction of cholesterol storage, and we found that this was associated with enhanced exit of the NPC1 protein from the endoplasmic reticulum and delivery to LE/Ly.
                                        HSP90 inhibitors reduce cholesterol storage in Niemann-Pick type C1 mutant fibroblasts
                                      • Research Article
                                        Open Access

                                        Red blood cell triglycerides—a unique pool that incorporates plasma-free fatty acids and relates to metabolic health

                                        Journal of Lipid Research
                                        Vol. 62100131Published online: October 3, 2021
                                        • Yilin Song
                                        • Michael D. Jensen
                                        Cited in Scopus: 0
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                                          Most research into red blood cell (RBC) lipids focuses on membrane phospholipids and their relationships to metabolic conditions and diet. Triglycerides (TGs) exist in most cells; the TG-fatty acids serve as readily available fuel for oxidative phosphorylation. Because RBCs lack mitochondria, they would not be expected to store fatty acids in TG. We followed up on a previous in vitro study that found FFA can be incorporated into RBC-TG by testing whether intravenously infused [U-13C]palmitate could be detected in RBC-TG.
                                          Red blood cell triglycerides—a unique pool that incorporates plasma-free fatty acids and relates to metabolic health
                                        • Research Article
                                          Open Access

                                          Human cholesteryl ester transfer protein lacks lipopolysaccharide transfer activity, but worsens inflammation and sepsis outcomes in mice

                                          Journal of Lipid Research
                                          Vol. 62100011Published online: December 15, 2020
                                          • Aloïs Dusuel
                                          • Valérie Deckert
                                          • Jean-Paul Pais de Barros
                                          • Kevin van Dongen
                                          • Hélène Choubley
                                          • Émilie Charron
                                          • and others
                                          Cited in Scopus: 0
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                                            Bacterial lipopolysaccharides (LPSs or endotoxins) can bind most proteins of the lipid transfer/LPS-binding protein (LT/LBP) family in host organisms. The LPS-bound LT/LBP proteins then trigger either an LPS-induced proinflammatory cascade or LPS binding to lipoproteins that are involved in endotoxin inactivation and detoxification. Cholesteryl ester transfer protein (CETP) is an LT/LBP member, but its impact on LPS metabolism and sepsis outcome is unclear. Here, we performed fluorescent LPS transfer assays to assess the ability of CETP to bind and transfer LPS.
                                            Human cholesteryl ester transfer protein lacks lipopolysaccharide transfer activity, but worsens inflammation and sepsis outcomes in mice
                                          • Research Article
                                            Open Access

                                            Generation and validation of a conditional knockout mouse model for the study of the Smith-Lemli-Opitz syndrome

                                            Journal of Lipid Research
                                            Vol. 62100002Published online: November 22, 2020
                                            • Babunageswararao Kanuri
                                            • Vincent Fong
                                            • Sithara Raju Ponny
                                            • Keri A. Tallman
                                            • Sriganesh Ramachandra Rao
                                            • Ned Porter
                                            • and others
                                            Cited in Scopus: 0
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                                              Smith-Lemli-Opitz Syndrome (SLOS) is a developmental disorder (OMIM # 270400 ) caused by autosomal recessive mutations in the Dhcr7 gene, which encodes the enzyme 3β-hydroxysterol-Δ7 reductase. SLOS patients present clinically with dysmorphology and neurological, behavioral, and cognitive defects, with characteristically elevated levels of 7-dehydrocholesterol (7-DHC) in all bodily tissues and fluids. Previous mouse models of SLOS have been hampered by postnatal lethality when Dhcr7 is knocked out globally, while a hypomorphic mouse model showed improvement in the biochemical phenotype with aging and did not manifest most other characteristic features of SLOS.
                                              Generation and validation of a conditional knockout mouse model for the study of the Smith-Lemli-Opitz syndrome
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