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  1. Article ; Online: Stearoyl-CoA desaturase 5 (SCD5), a Δ-9 fatty acyl desaturase in search of a function.

    Igal, R Ariel / Sinner, Débora I

    Biochimica et biophysica acta. Molecular and cell biology of lipids

    2020  Volume 1866, Issue 1, Page(s) 158840

    Abstract: A large body of research has demonstrated that human stearoyl-CoA desaturase 1 (SCD1), a universally expressed fatty acid Δ9-desaturase that converts saturated fatty acids (SFA) into monounsaturated fatty acids (MUFA), is a central regulator of metabolic ...

    Abstract A large body of research has demonstrated that human stearoyl-CoA desaturase 1 (SCD1), a universally expressed fatty acid Δ9-desaturase that converts saturated fatty acids (SFA) into monounsaturated fatty acids (MUFA), is a central regulator of metabolic and signaling pathways involved in cell proliferation, differentiation, and survival. Unlike SCD1, stearoyl-CoA desaturase 5 (SCD5), a second SCD isoform found in a variety of vertebrates, including humans, has received considerably less attention but new information on the catalytic properties, regulation and biological functions of this enzyme has begun to emerge. This review will examine the new evidence that supports key metabolic and biological roles for SCD5, as well as the potential implication of this desaturase in the mechanisms of human diseases.
    MeSH term(s) Amino Acid Sequence ; Animals ; Cell Survival ; Cleft Palate/enzymology ; Cleft Palate/genetics ; Cleft Palate/pathology ; Fatty Acids/metabolism ; Fatty Acids, Monounsaturated/metabolism ; Gene Expression Regulation ; Humans ; Lipid Metabolism/genetics ; Neoplasms/enzymology ; Neoplasms/genetics ; Neoplasms/pathology ; Neurodegenerative Diseases/enzymology ; Neurodegenerative Diseases/genetics ; Neurodegenerative Diseases/pathology ; Sequence Alignment ; Sequence Homology, Amino Acid ; Signal Transduction ; Stearoyl-CoA Desaturase/genetics ; Stearoyl-CoA Desaturase/metabolism
    Chemical Substances Fatty Acids ; Fatty Acids, Monounsaturated ; SCD1 protein, human (EC 1.14.19.1) ; SCD5 protein, human (EC 1.14.19.1) ; Stearoyl-CoA Desaturase (EC 1.14.19.1)
    Language English
    Publishing date 2020-10-10
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 60-7
    ISSN 1879-2618 ; 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1879-2618 ; 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/j.bbalip.2020.158840
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Stearoyl-CoA desaturase 5 (SCD5), a Δ-9 fatty acyl desaturase in search of a function

    Igal, R. Ariel / Sinner, Débora I

    Biochimica et biophysica acta. 2021 Jan., v. 1866, no. 1

    2021  

    Abstract: A large body of research has demonstrated that human stearoyl-CoA desaturase 1 (SCD1), a universally expressed fatty acid Δ9-desaturase that converts saturated fatty acids (SFA) into monounsaturated fatty acids (MUFA), is a central regulator of metabolic ...

    Abstract A large body of research has demonstrated that human stearoyl-CoA desaturase 1 (SCD1), a universally expressed fatty acid Δ9-desaturase that converts saturated fatty acids (SFA) into monounsaturated fatty acids (MUFA), is a central regulator of metabolic and signaling pathways involved in cell proliferation, differentiation, and survival. Unlike SCD1, stearoyl-CoA desaturase 5 (SCD5), a second SCD isoform found in a variety of vertebrates, including humans, has received considerably less attention but new information on the catalytic properties, regulation and biological functions of this enzyme has begun to emerge. This review will examine the new evidence that supports key metabolic and biological roles for SCD5, as well as the potential implication of this desaturase in the mechanisms of human diseases.
    Keywords cell proliferation ; humans ; stearoyl-CoA desaturase
    Language English
    Dates of publication 2021-01
    Publishing place Elsevier B.V.
    Document type Article
    Note NAL-AP-2-clean
    ISSN 1388-1981
    DOI 10.1016/j.bbalip.2020.158840
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: In Reference to Establishing an Endoscopic Chronic Subglottic Stenosis Rabbit Model.

    Katz Kadosh, Orna / Nebor, Ivanna / Smith, Matthew M / Hart, Catherine K / Tabangin, Meredith E / Burra, Kaulini / Kasten, Jennifer L / Sinner, Debora I / de Alarcon, Alessandro

    The Laryngoscope

    2023  Volume 133, Issue 5, Page(s) E32

    MeSH term(s) Animals ; Rabbits ; Constriction, Pathologic ; Endoscopy ; Laryngostenosis/etiology ; Laryngostenosis/surgery
    Language English
    Publishing date 2023-03-01
    Publishing country United States
    Document type Letter ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 80180-x
    ISSN 1531-4995 ; 0023-852X
    ISSN (online) 1531-4995
    ISSN 0023-852X
    DOI 10.1002/lary.30548
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Establishing an Endoscopic Chronic Subglottic Stenosis Rabbit Model.

    Kadosh, Orna K / Nebor, Ivanna / Smith, Matthew M / Hart, Catherine K / Tabangin, Meredith E / Burra, Kaulini / Kasten, Jennifer L / Sinner, Debora I / de Alarcon, Alessandro

    The Laryngoscope

    2021  Volume 132, Issue 10, Page(s) 1909–1915

    Abstract: Objectives/hypothesis: To develop a reproducible and consistent chronic subglottic stenosis (SGS) in an endoscopic animal model.: Study design: Prospective study.: Methods: We conducted a prospective study using New Zealand white rabbits. Chronic ... ...

    Abstract Objectives/hypothesis: To develop a reproducible and consistent chronic subglottic stenosis (SGS) in an endoscopic animal model.
    Study design: Prospective study.
    Methods: We conducted a prospective study using New Zealand white rabbits. Chronic SGS was induced endoscopically by Bugbee electrocautery to 50% to 75% of the subglottic area's circumference, followed by 4-hour endotracheal intubation. The rabbit airways were endoscopically assessed and sized with uncuffed endotracheal tubes (ETTs) before the injury, during follow-up, and at the endpoints. There were four endpoints: 2, 4, 6, and 8 weeks post SGS induction. Animals were humanely euthanized for histopathological examination of the subglottic injury site and microscopic measurement of the cricoid lumen.
    Results: Twenty-two rabbits reached the endpoints, and 18 rabbits developed chronic SGS. ETT size significantly decreased by 0.5 from preinjury to the endpoint in all groups, P < .001. Control median cricoid lumen measurements were 20.48 mm
    Conclusion: We developed an animal model to study chronic SGS. This model will be utilized to compare different endoscopic treatment interventions in acute SGS versus chronic SGS and further define the molecular basis of SGS.
    Level of evidence: NA Laryngoscope, 132:1909-1915, 2022.
    MeSH term(s) Animals ; Collagen ; Constriction, Pathologic ; Disease Models, Animal ; Laryngostenosis/pathology ; Prospective Studies ; Rabbits
    Chemical Substances Collagen (9007-34-5)
    Language English
    Publishing date 2021-10-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80180-x
    ISSN 1531-4995 ; 0023-852X
    ISSN (online) 1531-4995
    ISSN 0023-852X
    DOI 10.1002/lary.29873
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: StearoylCoA desaturase-5: a novel regulator of neuronal cell proliferation and differentiation.

    Sinner, Debora I / Kim, Gretchun J / Henderson, Gregory C / Igal, R Ariel

    PloS one

    2012  Volume 7, Issue 6, Page(s) e39787

    Abstract: Recent studies have demonstrated that human stearoylCoA desaturase-1 (SCD1), a Δ9-desaturase that converts saturated fatty acids (SFA) into monounsaturated fatty acids, controls the rate of lipogenesis, cell proliferation and tumorigenic capacity in ... ...

    Abstract Recent studies have demonstrated that human stearoylCoA desaturase-1 (SCD1), a Δ9-desaturase that converts saturated fatty acids (SFA) into monounsaturated fatty acids, controls the rate of lipogenesis, cell proliferation and tumorigenic capacity in cancer cells. However, the biological function of stearoylCoA desaturase-5 (SCD5), a second isoform of human SCD that is highly expressed in brain, as well as its potential role in human disease, remains unknown. In this study we report that the constitutive overexpression of human SCD5 in mouse Neuro2a cells, a widely used cell model of neuronal growth and differentiation, displayed a greater n-7 MUFA-to-SFA ratio in cell lipids compared to empty-vector transfected cells (controls). De novo synthesis of phosphatidylcholine and cholesterolesters was increased whereas phosphatidylethanolamine and triacylglycerol formation was reduced in SCD5-expressing cells with respect to their controls, suggesting a differential use of SCD5 products for lipogenic reactions. We also observed that SCD5 expression markedly accelerated the rate of cell proliferation and suppressed the induction of neurite outgrowth, a typical marker of neuronal differentiation, by retinoic acid indicating that the desaturase plays a key role in the mechanisms of cell division and differentiation. Critical signal transduction pathways that are known to modulate these processes, such epidermal growth factor receptor (EGFR)Akt/ERK and Wnt, were affected by SCD5 expression. Epidermal growth factor-induced phosphorylation of EGFR, Akt and ERK was markedly blunted in SCD5-expressing cells. Furthermore, the activity of canonical Wnt was reduced whereas the non-canonical Wnt was increased by the presence of SCD5 activity. Finally, SCD5 expression increased the secretion of recombinant Wnt5a, a non-canonical Wnt, whereas it reduced the cellular and secreted levels of canonical Wnt7b. Our data suggest that, by a coordinated modulation of key lipogenic pathways and transduction signaling cascades, SCD5 participates in the regulation of neuronal cell growth and differentiation.
    MeSH term(s) Animals ; Cell Differentiation/physiology ; Cell Line ; Cell Line, Tumor ; Cell Proliferation ; Fatty Acids/metabolism ; Humans ; Mice ; Stearoyl-CoA Desaturase/genetics ; Stearoyl-CoA Desaturase/metabolism
    Chemical Substances Fatty Acids ; SCD5 protein, human (EC 1.14.19.1) ; Stearoyl-CoA Desaturase (EC 1.14.19.1)
    Language English
    Publishing date 2012-06-22
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0039787
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Complete Tracheal Ring Deformity. A Translational Genomics Approach to Pathogenesis.

    Sinner, Debora I / Carey, Brenna / Zgherea, Daniela / Kaufman, K M / Leesman, Lauren / Wood, Robert E / Rutter, Michael J / de Alarcon, Alessandro / Elluru, Ravindhra G / Harley, John B / Whitsett, Jeffrey A / Trapnell, Bruce C

    American journal of respiratory and critical care medicine

    2019  Volume 200, Issue 10, Page(s) 1267–1281

    Abstract: Rationale: ...

    Abstract Rationale:
    MeSH term(s) Animals ; Cohort Studies ; Disease Models, Animal ; Humans ; Mice ; Mutation/genetics ; Respiratory System Abnormalities/diagnosis ; Respiratory System Abnormalities/genetics ; Respiratory System Abnormalities/surgery ; Trachea/abnormalities
    Language English
    Publishing date 2019-05-31
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1180953-x
    ISSN 1535-4970 ; 0003-0805 ; 1073-449X
    ISSN (online) 1535-4970
    ISSN 0003-0805 ; 1073-449X
    DOI 10.1164/rccm.201809-1626OC
    Database MEDical Literature Analysis and Retrieval System OnLINE

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