Component

Placental-cell iron uptake

Placental-cell iron uptake

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Suppressing endogenous human ZIP8 in BeWo placental cells reduced iron uptake by approximately 40%.

    Human ZIP8 (SLC39A8) → Placental-cell iron uptake source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    cross_nutrient
    true
    experimental_model
    ZIP8 suppression in BeWo trophoblast-derived cells
    exposure
    Endogenous ZIP8 knockdown compared with controls.
    limitations
    This is iron uptake in a placental cell line, not direct transplacental zinc flux or an in vivo fetal iron requirement for dietary zinc.
    nutrient_topic
    Zinc research collection; topical membership is not evidence of a direct dietary effect. · Zinc
    organism
    Homo sapiens
    plain_language
    ZIP8 contributed to iron entry in a human placental cell model.
    primary_references
    [zinc-trans-22898811] ZIP8 is an iron and zinc transporter whose cell-surface expression is up-regulated by cellular iron loading. (2012). https://pubmed.ncbi.nlm.nih.gov/22898811/ DOI: 10.1074/jbc.m112.367284
    tissue_or_cell_type
    BeWo placental cell line
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Zinc: transport, enzyme loading, deficiency and nutrient interactions (2026-09-17) · lines 466–477

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · ZIP8 suppression in BeWo trophoblast-derived cells · source_derived_draft · unverified_draft

    ### zinc-trans-zip8-placental-iron Suppressing endogenous human ZIP8 in BeWo placental cells reduced iron uptake by approximately 40%. Condition category: machinery_impairment nutrient_topic: Zinc research collection; topical membership is not evidence of a direct dietary effect. plain_language: ZIP8 contributed to iron entry in a human placental cell model. organism: Homo sapiens tissue_or_cell_type: BeWo placental cell line experimental_model: ZIP8 suppression in BeWo trophoblast-derived cells limitations: This is iron uptake in a placental cell line, not direct transplacental zinc flux or an in vivo fetal iron requirement for dietary zinc. exposure: Endogenous ZIP8 knockdown compared with controls. cross_nutrient: true [zinc-trans-22898811] ZIP8 is an iron and zinc transporter whose cell-surface expression is up-regulated by cellular iron loading. (2012). https://pubmed.ncbi.nlm.nih.gov/22898811/ DOI: 10.1074/jbc.m112.367284
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards