Component

Human TRPM2

Human calcium-permeable cation channel; historically LTRPC2.

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. Intracellular free ADP-ribose gated calcium-permeable currents in HEK293 cells expressing human TRPM2/LTRPC2.

    ADP-ribose → Human TRPM2 source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    true
    evidence_span
    {"source_cache": "artifacts/niacin-consumption-sources/trpm2001.abstract.txt", "locator": "Indexed abstract", "start_char": 0, "end_char": 964, "file_sha256": "960106d86cb7e891772139bf3b6339a1e50129c93a9e3517ebc7b86d61b4178e", "text_sha256": "960106d86cb7e891772139bf3b6339a1e50129c93a9e3517ebc7b86d61b4178e"}
    experimental_model
    Whole-cell and single-channel electrophysiology
    exposure
    Intracellular free ADP-ribose
    limitations
    This establishes channel gating in the assay, not that all NAD cleavage causes calcium influx in vivo.
    nutrient_topic
    Niacin research collection; topical membership is not evidence of a direct dietary effect. · Niacin (vitamin B3)
    organism
    Human
    plain_language
    Free ADP-ribose can open a channel that conducts calcium.
    primary_references
    [b3-cons-trpm2001] ADP-ribose gating of the calcium-permeable LTRPC2 channel revealed by Nudix motif homology. (2001). https://pubmed.ncbi.nlm.nih.gov/11385575/ DOI: 10.1038/35079100
    tissue_or_cell_type
    HEK293 cells expressing recombinant TRPM2

    Niacin: NAD metabolism, deficiency and nutrient interactions (2026-09-17) · lines 621–633

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Whole-cell and single-channel electrophysiology · source_derived_draft · unverified_draft

    ### b3-cons-adpr-trpm2-gating Intracellular free ADP-ribose gated calcium-permeable currents in HEK293 cells expressing human TRPM2/LTRPC2. Condition category: normal nutrient_topic: Niacin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Free ADP-ribose can open a channel that conducts calcium. organism: Human tissue_or_cell_type: HEK293 cells expressing recombinant TRPM2 experimental_model: Whole-cell and single-channel electrophysiology limitations: This establishes channel gating in the assay, not that all NAD cleavage causes calcium influx in vivo. exposure: Intracellular free ADP-ribose cross_nutrient: true evidence_span: {"source_cache": "artifacts/niacin-consumption-sources/trpm2001.abstract.txt", "locator": "Indexed abstract", "start_char": 0, "end_char": 964, "file_sha256": "960106d86cb7e891772139bf3b6339a1e50129c93a9e3517ebc7b86d61b4178e", "text_sha256": "960106d86cb7e891772139bf3b6339a1e50129c93a9e3517ebc7b86d61b4178e"} [b3-cons-trpm2001] ADP-ribose gating of the calcium-permeable LTRPC2 channel revealed by Nudix motif homology. (2001). https://pubmed.ncbi.nlm.nih.gov/11385575/ DOI: 10.1038/35079100
    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