Evidence map›Paper›PMID 38383607›Full record

ArticleNature communications2024

Intestinal IL-22RA1 signaling regulates intrinsic and systemic lipid and glucose metabolism to alleviate obesity-associated disorders.

Stephen J Gaudino, Ankita Singh, Huakang Huang, Jyothi Padiadpu, Makheni Jean-Pierre, Cody Kempen, Tej Bahadur, Kiyoshi Shiomitsu, Richard Blumberg, Kenneth R Shroyer and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
15.4field-weighted citation impact, top 1% of its field
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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Anti-Obesity Effects Exerted byFood science & nutrition · 2025
    Article
  8. Review
  9. iMeta · 2025
    Article
  10. Review
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  15. 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

14 authors at 4 institutions in 1 country.

Stephen J GaudinoDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Ankita SinghDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Huakang HuangDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Jyothi PadiadpuCollege of Pharmacy, Oregon State University, Corvallis, OR, USA.ORCID 0000-0002-9507-6133
Makheni Jean-PierreDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Cody KempenDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Tej BahadurDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Kiyoshi ShiomitsuDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.ORCID 0009-0000-6427-1721
Richard BlumbergDepartment of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.ORCID 0000-0002-9704-248X
Kenneth R ShroyerDepartment of Pathology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Semir BeyazCold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
Natalia ShulzhenkoCarlson College of Veterinary Medicine, Oregon State University, Corvallis, OR, USA.ORCID 0000-0003-0077-8456
Andrey MorgunCollege of Pharmacy, Oregon State University, Corvallis, OR, USA.ORCID 0000-0002-8924-6108
Pawan KumarDepartment of Microbiology and Immunology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA. pawan.kumar@stonybrook.edu.
Stony Brook School · USOregon State University · USBrigham and Women's Hospital · USCold Spring Harbor Laboratory · US

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI John Edward Moses · 1987 to 2026
$118.9M
MOLECULAR AND CELL BIOLOGY OF INFECTIOUS DISEASEST32AI007539 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI KONOPKA, JAMES B · 1998 to 2023
$3.6M
Intestinal IL-17RA signaling and mucosal host defenseR01DK121798 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI KUMAR, PAWAN · 2019 to 2023
$2.1M
Gut microbiota mediates the interplay between immunity and glucose metabolismR01DK103761 · NIDDK · OREGON STATE UNIVERSITY · PI SHULZHENKO, NATALIA · 2015 to 2019
$1.7M
Investigating the role of Akkermansia muciniphila and intestinal IL-17RA signaling in autoimmune inflammationR21AI146696 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI KUMAR, PAWAN · 2019 to 2020
$432k
Paneth cell-specific IL-22Ra1 signaling in mucosal host defenseR21AI149257 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI KUMAR, PAWAN · 2020 to 2021
$432k
NCI NIH HHS P30 CA045508NIAID NIH HHS R21 AI146696NIAID NIH HHS R21 AI149257NIAID NIH HHS T32 AI007539NIDDK NIH HHS R01 DK103761NIDDK NIH HHS R01 DK121798U.S. Department of Health & Human Services | National Institutes of Health (NIH) AI149257U.S. Department of Health & Human Services | National Institutes of Health (NIH) T32AI007539
6 · The paper itself

Abstract

IL-22 is critical for ameliorating obesity-induced metabolic disorders. However, it is unknown where IL-22 acts to mediate these outcomes. Here we examine the importance of tissue-specific IL-22RA1 signaling in mediating long-term high fat diet (HFD) driven metabolic disorders. To do so, we generated intestinal epithelium-, liver-, and white adipose tissue (WAT)-specific Il22ra1 knockout and littermate control mice. Intestinal epithelium- and liver-specific IL-22RA1 signaling upregulated systemic glucose metabolism. Intestinal IL-22RA1 signaling also mediated liver and WAT metabolism in a microbiota-dependent manner. We identified an association between Oscillibacter and elevated WAT inflammation, likely induced by Mmp12 expressing macrophages. Mechanistically, transcription of intestinal lipid metabolism genes is regulated by IL-22 and potentially IL-22-induced IL-18. Lastly, we show that Paneth cell-specific IL-22RA1 signaling, in part, mediates systemic glucose metabolism after HFD. Overall, these results elucidate a key role of intestinal epithelium-specific IL-22RA1 signaling in regulating intestinal metabolism and alleviating systemic obesity-associated disorders.

Indexed as

LiverMetabolic DiseasesAnimalsDiet, High-FatGlucoseInflammationLipid MetabolismLipidsMiceMice, Inbred C57BLObesityGlucoseLipids

Identifiers

PMID38383607
PMCPMC10881576
OpenAlexW4392090882

What OpenQuestion 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 OpenQuestion graph.