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Journal of Lipid Research
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    • July 2022 - January 2023Remove July 2022 - January 2023 filter
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    Article Type

    • Research Article3

    Author

    • Aoki, Junken1
    • Bogie, Jeroen FJ1
    • Chen, Wentong1
    • He, Xinyu1
    • He, Xueqing1
    • Hendriks, Jerome JA1
    • Hoeksema, Marten A1
    • Huang, Lei1
    • Jongejan, Aldo1
    • Kano, Kuniyuki1
    • Kawana, Hiroki1
    • Kingma, Jenina1
    • Kong, Qin1
    • Kono, Nozomu1
    • Li, Weizu1
    • Loix, Melanie1
    • Lu, Wenjie1
    • Meurs, Amber1
    • Onishi, Hirofumi1
    • Ottenhoff, Roelof1
    • Ozawa, Masaya1
    • Pasterkamp, Gerard1
    • Prange, Koen1
    • Sato, Yukitaka1
    • Shibata, Takeaki1

    Keyword

    • LPE3
    • 1-acyl lysophosphatidylcholine1
    • 1-acyl lysophosphatidylethanolamine1
    • 1-acyl phosphatidylcholine1
    • 1-acyl phosphatidylethanolamine1
    • 1-acylglycerol-3-phosphate-O-acyltransferase1
    • 1-O-alkenyl lysophosphatidylcholine1
    • 1-O-alkenyl lysophosphatidylethanolamine1
    • 1-O-alkenyl phosphatidylcholine1
    • 1-O-alkenyl phosphatidylethanolamine1
    • 1-O-alkyl lysophosphatidylcholine1
    • 1-O-alkyl lysophosphatidylethanolamine1
    • 31-deuterium-labeled palmitic acid1
    • 35-deuterium-labeled stearic acid1
    • 9-deuterium-labeled oleic acid1
    • ABCA11
    • Acetylated LDL1
    • AcLDL1
    • ADH1
    • AGPAT1
    • Alcohol dehydrogenase1
    • ALT1
    • AST1
    • ATP Binding Cassette Subfamily A Member 11
    • ATP synthesis1

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    • Research Article
      Open Access

      Phosphoethanolamine cytidylyltransferase ameliorates mitochondrial function and apoptosis in hepatocytes in T2DM in vitro

      Journal of Lipid Research
      Vol. 64Issue 3100337Published online: January 27, 2023
      • Hu Xu
      • Weizu Li
      • Lei Huang
      • Xinyu He
      • Bei Xu
      • Xueqing He
      • and others
      Cited in Scopus: 0
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        Liver function indicators are often impaired in patients with type 2 diabetes mellitus (T2DM), who present higher concentrations of aspartate aminotransferase, alanine aminotransferase, and gamma-glutamyl transferase than individuals without diabetes. However, the mechanism of liver injury in patients with T2DM has not been clearly elucidated. In this study, we performed a lipidomics analysis on the liver of T2DM mice, and we found that phosphatidylethanolamine (PE) levels were low in T2DM, along with an increase in diglyceride, which may be due to a decrease in the levels of phosphoethanolamine cytidylyltransferase (Pcyt2), thus likely affecting the de novo synthesis of PE.
        Phosphoethanolamine cytidylyltransferase ameliorates mitochondrial function and apoptosis in hepatocytes in T2DM in vitro
      • Research Article
        Open Access

        Sterol-regulated transmembrane protein TMEM86a couples LXR signaling to regulation of lysoplasmalogens in macrophages

        Journal of Lipid Research
        Vol. 64Issue 2100325Published online: December 30, 2022
        • Suzanne A.E. van Wouw
        • Marlene van den Berg
        • Maroua El Ouraoui
        • Amber Meurs
        • Jenina Kingma
        • Roelof Ottenhoff
        • and others
        Cited in Scopus: 0
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          Lysoplasmalogens are a class of vinyl ether bioactive lipids that have a central role in plasmalogen metabolism and membrane fluidity. The liver X receptor (LXR) transcription factors are important determinants of cellular lipid homeostasis owing to their ability to regulate cholesterol and fatty acid metabolism. However, their role in governing the composition of lipid species such as lysoplasmalogens in cellular membranes is less well studied. Here, we mapped the lipidome of bone marrow–derived macrophages (BMDMs) following LXR activation.
          Sterol-regulated transmembrane protein TMEM86a couples LXR signaling to regulation of lysoplasmalogens in macrophages
        • Research Article
          Open Access

          Identification and characterization of LPLAT7 as an sn-1-specific lysophospholipid acyltransferase

          Journal of Lipid Research
          Vol. 63Issue 10100271Published online: August 29, 2022
          • Hiroki Kawana
          • Masaya Ozawa
          • Takeaki Shibata
          • Hirofumi Onishi
          • Yukitaka Sato
          • Kuniyuki Kano
          • and others
          Cited in Scopus: 0
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            The main fatty acids at the sn-1 position of phospholipids (PLs) are saturated or monounsaturated fatty acids such as palmitic acid (C16:0), stearic acid (C18:0), and oleic acid (C18:1) and are constantly replaced, like unsaturated fatty acids at the sn-2 position. However, little is known about the molecular mechanism underlying the replacement of fatty acids at the sn-1 position, i.e., the sn-1 remodeling. Previously, we established a method to evaluate the incorporation of fatty acids into the sn-1 position of lysophospholipids (lyso-PLs).
            Identification and characterization of LPLAT7 as an sn-1-specific lysophospholipid acyltransferase
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