Evidence map›Paper›PMID 41737207›Full record

ArticleFrontiers in immunology2026

Zinc suppresses Stat3-driven IL-6 production in primary mouse adipocytes.

Hak Chung, John Eom, Michelle Sma Damen, Traci E Stankiewicz, Keisuke Sawada, Pablo C Alarcon, Cassidy J Ulanowicz, Jennifer L Wayland, George S Deepe, Senad Divanovic

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Hak ChungDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
John EomDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Michelle Sma DamenDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Traci E StankiewiczDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Keisuke SawadaDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Pablo C AlarconDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Cassidy J UlanowiczDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Jennifer L WaylandDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
George S DeepeDivision of Infectious Diseases, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Senad DivanovicDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

Funding

PEDIATRIC GASTROENTEROLOGY AND NUTRITION TRAINING GRANTT32DK007727 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Phillip P Minar · 1995 to 2026
$11.3M
Contribution of adipocyte inflammation to parturition timingF30HD117460 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI Jennifer Lynne Wayland · 2025 to 2026
$98k
NICHD NIH HHS F30 HD117460NIDDK NIH HHS T32 DK007727
6 · The paper itself

Abstract

Uncontrolled inflammatory cytokine production promotes pathogenesis of various chronic diseases. Zinc (Zn) regulates immune cell inflammatory cytokine production. However, the influence of Zn on the inflammatory properties of non-immune cells known to contribute to disease pathogenesis is not well understood. Adipocytes respond to various immunological stimuli by activating inflammatory pathways and secreting inflammatory cytokines. Here, we investigated the impact of Zn on adipocyte inflammatory vigor. We show that treatment of primary mouse adipocytes with Zn, in the form of Zn pyrithione, restricted their toll-like receptor ligand-driven IL-6 production. Mechanistically, IL-6 secreted from adipocytes functions in an autocrine fashion to activate the Stat3 pathway and amplify IL-6 production via a positive feedback loop. Notably, Zn treatment of adipocytes suppressed Stat3 signaling activation to break the positive feedback loop and subsequent expression of IL-6 and its receptor genes (

Indexed as

AdipocytesInterleukin-6STAT3 Transcription FactorZincAnimalsCells, CulturedCytokine Receptor gp130Interleukin-6 Receptor alpha SubunitMiceReceptors, Interleukin-6Signal TransductionCytokine Receptor gp130Il6ra protein, mouseIl6st protein, mouseInterleukin-6interleukin-6, mouseInterleukin-6 Receptor alpha SubunitReceptors, Interleukin-6Stat3 protein, mouseSTAT3 Transcription FactorZincadipose tissuecytokinesimmunitymetalsobesitypyrithione

Identifiers

PMID41737207
PMCPMC12926143

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.