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Journal of Lipid Research
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    • Research Article5

    Author

    • Citir, Mevlut1
    • Cordes, Thekla1
    • Dauer, William T1
    • Dogan, Asli E1
    • Erbay, Ebru1
    • Gengatharan, Jivani1
    • Ginsberg, Henry N1
    • Hernandez-Ono, Antonio1
    • Hu, Qingzhe1
    • Kakiyama, Genta1
    • Khare, Sanika V1
    • Kuna, Ramya S1
    • McGregor, Grace H1
    • Metallo, Christian M1
    • Murai, Tsuyoshi1
    • Muthusamy, Thangaselvam1
    • Narushima, Seiko1
    • Nittono, Hiroshi1
    • Qin, Xinyue1
    • Sasaki, Takahiro1
    • Schultz, Carsten1
    • Shen, Guanru1
    • Shin, Ji-Yeon1
    • Suzuki, Mitsuyoshi1
    • Takei, Hajime1

    Keyword

    • high-fat diet2
    • (ATF)1
    • (CHOP)1
    • (CLPP)1
    • (eif2α)1
    • (ER)1
    • (GCN2)1
    • (HRI)1
    • (IRE1)1
    • (ISR)1
    • (LONP1)1
    • (mt)1
    • (mtHSP70)1
    • (PERK)1
    • (PKR)1
    • (RNase)1
    • (S1P)1
    • (SPL)1
    • (UPR)1
    • (Xbp1)1
    • 1-deoxy(dihydro)ceramide1
    • 1-deoxysphinganine1
    • 1-deoxysphingolipid accumulation1
    • AAV1
    • AAV-Cre1

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    • Research Article
      Open Access

      1-Deoxysphingolipid synthesis compromises anchorage-independent growth and plasma membrane endocytosis in cancer cells

      Journal of Lipid Research
      Vol. 63Issue 10100281Published online: September 14, 2022
      • Thekla Cordes
      • Ramya S. Kuna
      • Grace H. McGregor
      • Sanika V. Khare
      • Jivani Gengatharan
      • Thangaselvam Muthusamy
      • and others
      Cited in Scopus: 0
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        Serine palmitoyltransferase (SPT) predominantly incorporates serine and fatty acyl-CoAs into diverse sphingolipids (SLs) that serve as structural components of membranes and signaling molecules within or amongst cells. However, SPT also uses alanine as a substrate in the contexts of low serine availability, alanine accumulation, or disease-causing mutations in hereditary sensory neuropathy type I, resulting in the synthesis and accumulation of 1-deoxysphingolipids (deoxySLs). These species promote cytotoxicity in neurons and impact diverse cellular phenotypes, including suppression of anchorage-independent cancer cell growth.
        1-Deoxysphingolipid synthesis compromises anchorage-independent growth and plasma membrane endocytosis in cancer cells
      • Research Article
        Open Access

        Hepatocytes Deficient in Nuclear Envelope Protein Lamina-associated Polypeptide 1 are an Ideal Mammalian System to Study Intranuclear Lipid Droplets

        Journal of Lipid Research
        Vol. 63Issue 10100277Published online: September 9, 2022
        • Cecilia Östlund
        • Antonio Hernandez-Ono
        • Samantha J. Turk
        • William T. Dauer
        • Henry N. Ginsberg
        • Howard J. Worman
        • and others
        Cited in Scopus: 0
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          Lipid droplets (LDs) are generally considered to be synthesized in the ER and utilized in the cytoplasm. However, LDs have been observed inside nuclei in some cells, although recent research on nuclear LDs has focused on cultured cell lines. To better understand nuclear LDs that occur in vivo, here we examined LDs in primary hepatocytes from mice following depletion of the nuclear envelope protein lamina-associated polypeptide 1 (LAP1). Microscopic image analysis showed that LAP1-depleted hepatocytes contain frequent nuclear LDs, which differ from cytoplasmic LDs in their associated proteins.
          Hepatocytes Deficient in Nuclear Envelope Protein Lamina-associated Polypeptide 1 are an Ideal Mammalian System to Study Intranuclear Lipid Droplets
        • Research Article
          Open Access

          ER Stress-Induced Sphingosine-1-Phosphate Lyase Phosphorylation Potentiates the Mitochondrial Unfolded Protein Response

          Journal of Lipid Research
          Vol. 63Issue 10100279Published online: September 9, 2022
          • Asli D. Yildirim
          • Mevlut Citir
          • Asli E. Dogan
          • Zehra Veli
          • Zehra Yildirim
          • Ozlem Tufanli
          • and others
          Cited in Scopus: 0
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            The unfolded protein response (UPR) is an elaborate signaling network that evolved to maintain proteostasis in the endoplasmic reticulum (ER) and mitochondria (mt). These organelles are functionally and physically associated, and consequently, their stress responses are often intertwined. It is unclear how these two adaptive stress responses are coordinated during ER stress. The inositol-requiring enzyme-1 (IRE1), a central ER stress sensor and proximal regulator of the UPRER, harbors dual kinase and endoribonuclease (RNase) activities.
            ER Stress-Induced Sphingosine-1-Phosphate Lyase Phosphorylation Potentiates the Mitochondrial Unfolded Protein Response
          • Research Article
            Open Access

            Characterization of long-chain fatty acid-linked bile acids: a major conjugation form of 3β-hydroxy bile acids in feces

            Journal of Lipid Research
            Vol. 63Issue 10100275Published online: September 8, 2022
            • Hajime Takei
            • Seiko Narushima
            • Mitsuyoshi Suzuki
            • Genta Kakiyama
            • Takahiro Sasaki
            • Tsuyoshi Murai
            • and others
            Cited in Scopus: 0
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              Although most bile acids (BAs) in feces are present in noncovalent forms that can be extracted with ethanol, non-negligible amounts of saponifiable BAs are also present. It is a major concern that such saponifiable BAs are routinely omitted from fecal BA measurements. We compared the BA profiles of healthy stools that were obtained with/without alkaline hydrolysis and found that as much as 29.7% (2.1–67.7%) of total BAs were saponifiable. Specifically, alkaline treatment led to significant elevations of isodeoxycholic acid (isoDCA) and isolithocholic acid (isoLCA) concentrations, suggesting that considerable proportions of isoDCA and isoLCA were esterified.
              Characterization of long-chain fatty acid-linked bile acids: a major conjugation form of 3β-hydroxy bile acids in feces
            • Research Article
              Open Access

              RGMa promotes dedifferentiation of vascular smooth muscle cells into a macrophage-like phenotype in vivo and in vitro

              Journal of Lipid Research
              Vol. 63Issue 10100276Published online: September 8, 2022
              • Xiaofan Yuan
              • Hongmei Xiao
              • Qingzhe Hu
              • Guanru Shen
              • Xinyue Qin
              Cited in Scopus: 0
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                Repulsive guidance molecule a (RGMa) is a glycosylphosphatidylinositol-anchored glycoprotein that has been demonstrated to influence inflammatory-related diseases in addition to regulating neuronal differentiation and survival during brain development. However, any function or mechanism of RGMa in dedifferentiation of contractile vascular smooth muscle cells (VSMCs) during inflammatory-related atherosclerosis is poorly understood. In the current study, we found that RGMa is expressed in VSMCs-derived macrophage-like cells from the fibrous cap of type V atherosclerotic plaques and the neointima of ligated carotid artery in ApoE−/− mice.
                RGMa promotes dedifferentiation of vascular smooth muscle cells into a macrophage-like phenotype in vivo and in vitro
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