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  1. AU="Erdal, Ranya"
  2. AU="Li, Long-Xia"
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  1. Article: 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.
    Keywords brain ; gain-of-function mutation ; gene activation ; heme ; heme oxygenase (biliverdin-producing) ; iron ; mice ; neuroglia ; plasma membrane ; transferrin ; transferrin receptors
    Language English
    Dates of publication 2022-0804
    Size p. 2832-2843.e7.
    Publishing place Elsevier Inc.
    Document type Article
    ZDB-ID 1415236-8
    ISSN 1097-4164 ; 1097-2765
    ISSN (online) 1097-4164
    ISSN 1097-2765
    DOI 10.1016/j.molcel.2022.05.024
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; 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  Volume 82, Issue 19, Page(s) 3750

    Language English
    Publishing date 2022-10-08
    Publishing country United States
    Document type 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
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; 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  Volume 82, Issue 15, Page(s) 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 term(s) Animals ; Biological Transport ; Heme/genetics ; Heme/metabolism ; Iron/metabolism ; Mammals/metabolism ; Membrane Transport Proteins/metabolism ; Mice ; Organic Anion Transporters/metabolism ; Transcriptional Activation
    Chemical Substances Membrane Transport Proteins ; Organic Anion Transporters ; Slco2b1 protein, mouse ; Heme (42VZT0U6YR) ; Iron (E1UOL152H7)
    Language English
    Publishing date 2022-06-16
    Publishing country United States
    Document type 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
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Kategorien

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