Component

Human matrilin-2 / MATN2

Human matrilin-2 / MATN2. Species, exposure and limitations are retained in each linked claim.

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. MATN2 was identified as a primary SXR target responsive to vitamin K2 and rifampicin in osteoblastic cells.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/k2-research/16606623.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a2c0e756d507fd0cef9dea48e3eedc193084378509ec54bce2c097f8491e4b45", "start_char": 0, "end_char": 1266, "text_sha256": "a2c0e756d507fd0cef9dea48e3eedc193084378509ec54bce2c097f8491e4b45"}
    experimental_model
    Microarray, qPCR and gain/loss-of-function studies
    exposure
    Vitamin K2 and rifampicin/SXR stimulation
    limitations
    Cell transcription and collagen accumulation; not a human fracture study.
    nutrient_topic
    Vitamin K2 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin K2 / menaquinone family
    organism
    Human osteoblastic MG63 cells
    plain_language
    The receptor connects to a separately identifiable downstream gene.
    primary_references
    [k2-p16606623] Steroid and xenobiotic receptor SXR mediates vitamin K2-activated transcription of extracellular matrix-related genes and collagen accumulation in osteoblastic cells. (2006). https://pubmed.ncbi.nlm.nih.gov/16606623/ DOI: 10.1074/jbc.m600896200
    tissue_or_cell_type
    Extracellular-matrix gene regulation

    Vitamin K2: menaquinone forms, carboxylation, recycling and nutrient interactions (2026-09-17) · lines 734–745

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Microarray, qPCR and gain/loss-of-function studies · source_derived_draft · unverified_draft

    ### k2-sxr-matn2 MATN2 was identified as a primary SXR target responsive to vitamin K2 and rifampicin in osteoblastic cells. Condition category: normal nutrient_topic: Vitamin K2 research collection; topical membership is not evidence of a direct dietary effect. plain_language: The receptor connects to a separately identifiable downstream gene. organism: Human osteoblastic MG63 cells tissue_or_cell_type: Extracellular-matrix gene regulation experimental_model: Microarray, qPCR and gain/loss-of-function studies limitations: Cell transcription and collagen accumulation; not a human fracture study. exposure: Vitamin K2 and rifampicin/SXR stimulation evidence_span: {"source_cache": "artifacts/k2-research/16606623.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a2c0e756d507fd0cef9dea48e3eedc193084378509ec54bce2c097f8491e4b45", "start_char": 0, "end_char": 1266, "text_sha256": "a2c0e756d507fd0cef9dea48e3eedc193084378509ec54bce2c097f8491e4b45"} [k2-p16606623] Steroid and xenobiotic receptor SXR mediates vitamin K2-activated transcription of extracellular matrix-related genes and collagen accumulation in osteoblastic cells. (2006). https://pubmed.ncbi.nlm.nih.gov/16606623/ DOI: 10.1074/jbc.m600896200
    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