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  1. Artikel: Metabolic-scale gene activation screens identify SLCO2B1 as a heme transporter that enhances cellular iron availability

    Unlu, Gokhan / Prizer, Benjamin / Erdal, Ranya / Yeh, Hsi-Wen / Bayraktar, Erol C. / Birsoy, Kıvanç

    Molecular cell. 2022 Aug. 04, v. 82, no. 15

    2022  

    Abstract: Iron is the most abundant transition metal essential for numerous cellular processes. Although most mammalian cells acquire iron through transferrin receptors, molecular players of iron utilization under iron restriction are incompletely understood. To ... ...

    Abstract Iron is the most abundant transition metal essential for numerous cellular processes. Although most mammalian cells acquire iron through transferrin receptors, molecular players of iron utilization under iron restriction are incompletely understood. To address this, we performed metabolism-focused CRISPRa gain-of-function screens, which revealed metabolic limitations under stress conditions. Iron restriction screens identified not only expected members of iron utilization pathways but also SLCO2B1, a poorly characterized membrane carrier. SLCO2B1 expression is sufficient to increase intracellular iron, bypass the essentiality of the transferrin receptor, and enable proliferation under iron restriction. Mechanistically, SLCO2B1 mediates heme analog import in cellular assays. Heme uptake by SLCO2B1 provides sufficient iron for proliferation through heme oxygenases. Notably, SLCO2B1 is predominantly expressed in microglia in the brain, and primary Slco2b1⁻/⁻ mouse microglia exhibit strong defects in heme analog import. Altogether, our work identifies SLCO2B1 as a microglia-enriched plasma membrane heme importer and provides a genetic platform to identify metabolic limitations under stress conditions.
    Schlagwörter brain ; gain-of-function mutation ; gene activation ; heme ; heme oxygenase (biliverdin-producing) ; iron ; mice ; neuroglia ; plasma membrane ; transferrin ; transferrin receptors
    Sprache Englisch
    Erscheinungsverlauf 2022-0804
    Umfang p. 2832-2843.e7.
    Erscheinungsort Elsevier Inc.
    Dokumenttyp Artikel
    ZDB-ID 1415236-8
    ISSN 1097-4164 ; 1097-2765
    ISSN (online) 1097-4164
    ISSN 1097-2765
    DOI 10.1016/j.molcel.2022.05.024
    Datenquelle NAL Katalog (AGRICOLA)

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  2. Artikel ; Online: Metabolic-scale gene activation screens identify SLCO2B1 as a heme transporter that enhances cellular iron availability.

    Unlu, Gokhan / Prizer, Benjamin / Erdal, Ranya / Yeh, Hsi-Wen / Bayraktar, Erol C / Birsoy, Kıvanç

    Molecular cell

    2022  Band 82, Heft 19, Seite(n) 3750

    Sprache Englisch
    Erscheinungsdatum 2022-10-08
    Erscheinungsland United States
    Dokumenttyp Published Erratum
    ZDB-ID 1415236-8
    ISSN 1097-4164 ; 1097-2765
    ISSN (online) 1097-4164
    ISSN 1097-2765
    DOI 10.1016/j.molcel.2022.09.004
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Metabolic-scale gene activation screens identify SLCO2B1 as a heme transporter that enhances cellular iron availability.

    Unlu, Gokhan / Prizer, Benjamin / Erdal, Ranya / Yeh, Hsi-Wen / Bayraktar, Erol C / Birsoy, Kıvanç

    Molecular cell

    2022  Band 82, Heft 15, Seite(n) 2832–2843.e7

    Abstract: Iron is the most abundant transition metal essential for numerous cellular processes. Although most mammalian cells acquire iron through transferrin receptors, molecular players of iron utilization under iron restriction are incompletely understood. To ... ...

    Abstract Iron is the most abundant transition metal essential for numerous cellular processes. Although most mammalian cells acquire iron through transferrin receptors, molecular players of iron utilization under iron restriction are incompletely understood. To address this, we performed metabolism-focused CRISPRa gain-of-function screens, which revealed metabolic limitations under stress conditions. Iron restriction screens identified not only expected members of iron utilization pathways but also SLCO2B1, a poorly characterized membrane carrier. SLCO2B1 expression is sufficient to increase intracellular iron, bypass the essentiality of the transferrin receptor, and enable proliferation under iron restriction. Mechanistically, SLCO2B1 mediates heme analog import in cellular assays. Heme uptake by SLCO2B1 provides sufficient iron for proliferation through heme oxygenases. Notably, SLCO2B1 is predominantly expressed in microglia in the brain, and primary Slco2b1
    Mesh-Begriff(e) Animals ; Biological Transport ; Heme/genetics ; Heme/metabolism ; Iron/metabolism ; Mammals/metabolism ; Membrane Transport Proteins/metabolism ; Mice ; Organic Anion Transporters/metabolism ; Transcriptional Activation
    Chemische Substanzen Membrane Transport Proteins ; Organic Anion Transporters ; Slco2b1 protein, mouse ; Heme (42VZT0U6YR) ; Iron (E1UOL152H7)
    Sprache Englisch
    Erscheinungsdatum 2022-06-16
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1415236-8
    ISSN 1097-4164 ; 1097-2765
    ISSN (online) 1097-4164
    ISSN 1097-2765
    DOI 10.1016/j.molcel.2022.05.024
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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