Evidence map›Paper›PMID 39028754›Full record

ArticlePLoS biology2024

Signaling through the nicotinic acetylcholine receptor in the liver protects against the development of metabolic dysfunction-associated steatohepatitis.

Heejin Jun, Shanshan Liu, Alexander J Knights, Kezhou Zhu, Yingxu Ma, Jianke Gong, Ashley E Lenhart, Xiaoling Peng, Yunying Huang, Jared P Ginder and 6 more

Abstract read
In one paragraph

Article in PLoS biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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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

16 authors.

Heejin JunLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Shanshan LiuLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Alexander J KnightsLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Kezhou ZhuLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Yingxu MaLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Jianke GongLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Ashley E LenhartDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Xiaoling PengLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Yunying HuangLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Jared P GinderLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Christopher H DownieLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Erika Thalia RamosDepartment of Nutritional Sciences, College of Human Sciences, Texas Tech University, Lubbock, Texas, United States of America.
Klas KullanderDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Robert T KennedyDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan, United States of America.
X Z Shawn XuLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.
Jun WuLife Sciences Institute, University of Michigan, Ann Arbor, Michigan, United States of America.ORCID 0000-0003-4493-5820

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
TR&D 2 Metabolic Labels for Ultraplexed Protein Quantification p. 453P41GM108538 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI COON, JOSHUA J · 2016 to 2025
$13.1M
The role of immune-adipocyte cholinergic signaling during metabolic adaptation and dysfunctionR01DK107583 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WU, JUN · 2016 to 2024
$3.4M
MICROELECTRODE AND MICRODIALYSIS-BASED INSULIN SENSORSR01DK046960 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 1993 to 2020
$3.3M
A novel cholinergic circuitry in alcoholic liver disease (NIAAA)R01AA028761 · NIAAA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WU, JUN · 2021 to 2025
$2.1M
Chemosensation and longevity in C. elegansR01AG067753 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI XU, SHAWN · 2020 to 2024
$1.8M
Aberrant BCAA utilization in alcohol-induced metabolic dysregulationR15AA031123 · NIAAA · TEXAS TECH UNIVERSITY · PI JUN, HEEJIN · 2023 to 2023
$482k
NIAAA NIH HHS R01 AA028761NIAAA NIH HHS R15 AA031123NIA NIH HHS R01 AG067753NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK046960NIDDK NIH HHS R01 DK107583NIGMS NIH HHS P41 GM108538
6 · The paper itself

Abstract

Metabolic dysfunction-associated steatohepatitis (MASH) is the progressive form of liver steatosis, the most common liver disease, and substantially increases the mortality rate. However, limited therapies are currently available to prevent MASH development. Identifying potential pharmacological treatments for the condition has been hampered by its heterogeneous and complex nature. Here, we identified a hepatic nonneuronal cholinergic signaling pathway required for metabolic adaptation to caloric overload. We found that cholinergic receptor nicotinic alpha 2 subunit (CHRNA2) is highly expressed in hepatocytes of mice and humans. Further, CHRNA2 is activated by a subpopulation of local acetylcholine-producing macrophages during MASH development. The activation of CHRNA2 coordinates defensive programs against a broad spectrum of MASH-related pathogenesis, including steatosis, inflammation, and fibrosis. Hepatocyte-specific loss of CHRNA2 signaling accelerates the disease onset in different MASH mouse models. Activation of this pathway via pharmacological inhibition of acetylcholine degradation protects against MASH development. Our study uncovers a hepatic nicotinic cholinergic receptor pathway that constitutes a cell-autonomous self-defense route against prolonged metabolic stress and holds therapeutic potential for combatting human MASH.

Indexed as

Fatty LiverHepatocytesLiverReceptors, NicotinicSignal TransductionAcetylcholineAnimalsDisease Models, AnimalHumansMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutAcetylcholineReceptors, Nicotinic

Identifiers

PMID39028754
PMCPMC11290650

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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 OpenQuestion graph.