Component

Basal and maximal respiration in ergothioneine-treated human HeLa cells

2 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. MPST-deleted HeLa cells showed no significant respiratory increase with ergothioneine versus vehicle.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_access
    Publisher abstract/introduction plus the authors' article and supplementary legends reproduced in an indexed document. This is source-derived extraction, not raw-data verification. Main-text OCR corrupts some micro-unit symbols; ambiguous doses and binding constants are deliberately not transcribed.
    experimental_condition
    vehicle in MPST-deleted HeLa cells 500 micromolar, 72 hours · L-Ergothioneine Condition belongs to the full experimental contrast; do not separate a joint intervention.
    experimental_condition
    vehicle in MPST-deleted HeLa cells CRISPR-Cas9 deletion · Human mercaptopyruvate sulfurtransferase / MPST Condition belongs to the full experimental contrast; do not separate a joint intervention.
    experimental_contrast
    {"intervention": "ergothioneine in MPST-deleted HeLa cells", "comparator": "vehicle in MPST-deleted HeLa cells", "endpoint": "basal and maximal oxygen consumption", "effect_direction": "no_detected_change", "combination": "joint", "conditions": [{"entity_slug": "ergothioneine", "state": "500 micromolar, 72 hours"}, {"entity_slug": "mpst", "state": "CRISPR-Cas9 deletion"}]} Explicit extracted experimental comparison; source-derived draft.
    experimental_model
    CRISPR-Cas9 MPST-deleted human HeLa cells; 500 micromolar ergothioneine for 72 hours.
    interpretation_status
    Source-derived research curation; not independent raw-data verification.
    limitations
    The comparison is ergothioneine versus vehicle within knockout cells. It does not show that every protective action requires MPST, or that human dietary low intake mimics knockout.
    nutrient_topic
    Ergothioneine mitochondrial supplement; shared molecular requirements are not demonstrated dietary interactions. · L-Ergothioneine
    plain_language
    Loss of the target removed this measured response.
    primary_references
    Sprenger et al. Ergothioneine controls mitochondrial function and exercise performance via direct activation of MPST. DOI 10.1016/j.cmet.2025.01.024; PMID 39965563; https://pubmed.ncbi.nlm.nih.gov/39965563/
    source_locator
    Figures S2E-S2F; Results
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Ergothioneine: mitochondrial transport, MPST and sulfur-handling dependencies (2026-10-02) · lines 81–81

    Original AI-assisted curation of five primary studies with publication identifiers, experimental locators and access limitations. Additive chapter supplement, not publisher full text. · supports · CRISPR-Cas9 MPST-deleted human HeLa cells; 500 micromolar ergothioneine for 72 hours. · source_derived_draft · unverified_draft

    MPST-deleted HeLa cells showed no significant respiratory increase with ergothioneine versus vehicle.
    Complete structured claim and evidence
  2. Ergothioneine increased basal and maximal respiration in wild-type human HeLa cells.

    Experimental context and source evidence
    dose
    500 micromolar
    duration
    72 hours
    evidence_access
    Publisher abstract/introduction plus the authors' article and supplementary legends reproduced in an indexed document. This is source-derived extraction, not raw-data verification. Main-text OCR corrupts some micro-unit symbols; ambiguous doses and binding constants are deliberately not transcribed.
    experimental_condition
    vehicle in wild-type HeLa cells added · L-Ergothioneine Condition belongs to the full experimental contrast; do not separate a joint intervention.
    experimental_contrast
    {"intervention": "500 micromolar ergothioneine for 72 hours", "comparator": "vehicle in wild-type HeLa cells", "endpoint": "basal and maximal oxygen consumption", "effect_direction": "increase", "combination": "single", "conditions": [{"entity_slug": "ergothioneine", "state": "added"}]} Explicit extracted experimental comparison; source-derived draft.
    experimental_model
    Human HeLa cells; 500 micromolar ergothioneine for 72 hours, as stated unambiguously in supplementary Figure S2.
    interpretation_status
    Source-derived research curation; not independent raw-data verification.
    limitations
    Cancer-cell culture at this exposure is not a clinical supplementation result or proof of a nutritional requirement.
    nutrient_topic
    Ergothioneine mitochondrial supplement; shared molecular requirements are not demonstrated dietary interactions. · L-Ergothioneine
    organism
    Homo sapiens
    plain_language
    A human cell model showed a respiratory response.
    primary_references
    Sprenger et al. Ergothioneine controls mitochondrial function and exercise performance via direct activation of MPST. DOI 10.1016/j.cmet.2025.01.024; PMID 39965563; https://pubmed.ncbi.nlm.nih.gov/39965563/
    source_locator
    Figure S2E, wild-type panels

    Ergothioneine: mitochondrial transport, MPST and sulfur-handling dependencies (2026-10-02) · lines 73–73

    Original AI-assisted curation of five primary studies with publication identifiers, experimental locators and access limitations. Additive chapter supplement, not publisher full text. · supports · Human HeLa cells; 500 micromolar ergothioneine for 72 hours, as stated unambiguously in supplementary Figure S2. · source_derived_draft · unverified_draft

    Ergothioneine increased basal and maximal respiration in wild-type human HeLa cells.
    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