Evidence map›Paper›PMID 36169399›Full record

ArticleeLife2022

Phosphoproteomic mapping reveals distinct signaling actions and activation of muscle protein synthesis by Isthmin-1.

Meng Zhao, Niels Banhos Danneskiold-Samsøe, Livia Ulicna, Quennie Nguyen, Laetitia Voilquin, David E Lee, James P White, Zewen Jiang, Nickeisha Cuthbert, Shrika Paramasivam and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. 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
0.9field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Advances in Adipose Tissue Biology.Endocrine reviews · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Advances in research of biological functions of Isthmin-1.Journal of cell communication and signaling · 2023
    Review
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

13 authors at 4 institutions in 1 country.

Meng ZhaoDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.ORCID 0000-0002-5415-8335
Niels Banhos Danneskiold-SamsøeDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.
Livia UlicnaDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.
Quennie NguyenDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.
Laetitia VoilquinDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.ORCID 0000-0003-2138-4819
David E LeeDuke Molecular Physiology Institute, Duke University School of Medicine, Durham, United States.
James P WhiteDuke Molecular Physiology Institute, Duke University School of Medicine, Durham, United States.
Zewen JiangDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.ORCID 0000-0002-3852-8666
Nickeisha CuthbertDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.
Shrika ParamasivamDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.
Ewa Bielczyk-MaczynskaStanford Diabetes Research Center, Stanford University School of Medicine, Stanford, United States.ORCID 0000-0002-0558-1188
Capucine Van RechemDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.ORCID 0000-0002-5408-6124
Katrin J SvenssonDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.ORCID 0000-0001-5376-5128
Stanford University · USCardiovascular Institute of the South · USDuke University · USUniversity of California, San Francisco · US

Funding

Stanford Islet Research CoreP30DK116074 · NIDDK · STANFORD UNIVERSITY · PI Seung K Kim · 2017 to 2026
$19.5M
TRANSFUSION MEDICINE AND RELATED AREAST32HL007057 · NHLBI · DUKE UNIVERSITY · PI Gowthami M Arepally · 1985 to 2026
$10.6M
Mechanisms controlling fructose uptake and utilizationR01DK125260 · NIDDK · STANFORD UNIVERSITY · PI Katrin Jennifer Svensson · 2020 to 2026
$3.5M
The AMPK/ULK1/p27Kip1 axis regulates autophagy and cell survival in aged satellite cellsK01AG056664 · NIA · DUKE UNIVERSITY · PI WHITE, JAMES P. · 2017 to 2022
$913k
The role of circulating Slit2 in adipose thermogenesis and diabetesR00DK111916 · NIDDK · STANFORD UNIVERSITY · PI SVENSSON, KATRIN JENNIFER · 2018 to 2020
$731k
Assessing healthspan and epigenetics in aged mice after prolonged exposure to young circulationR21AG065943 · NIA · DUKE UNIVERSITY · PI WHITE, JAMES P. · 2020 to 2021
$443k
The role of circulating Slit2 in adipose thermogenesis and diabetesK99DK111916 · NIDDK · DANA-FARBER CANCER INST · PI SVENSSON, KATRIN JENNIFER · 2016 to 2017
$180k
ISOLATION OF D14Q23 FAMILIAL ALZHEIMER DISEASE LOCUSF32AG005666 · NIA · ELEANOR ROOSEVELT INST FOR CANCER RES · PI CLANCY, KEVIN P · 1994 to 1996
–
American Heart Association-American Stroke Association 18POST34030448NHLBI NIH HHS T32 HL007057NIA NIH HHS F32 AG005666NIA NIH HHS K01 AG056664NIA NIH HHS R21 AG065943NIDDK NIH HHS K99 DK111916NIDDK NIH HHS P30 DK116074NIDDK NIH HHS R00 DK111916NIDDK NIH HHS R01 DK125260
6 · The paper itself

Abstract

The secreted protein isthmin-1 (Ism1) mitigates diabetes by increasing adipocyte and skeletal muscle glucose uptake by activating the PI3K-Akt pathway. However, while both Ism1 and insulin converge on these common targets, Ism1 has distinct cellular actions suggesting divergence in downstream intracellular signaling pathways. To understand the biological complexity of Ism1 signaling, we performed phosphoproteomic analysis after acute exposure, revealing overlapping and distinct pathways of Ism1 and insulin. We identify a 53% overlap between Ism1 and insulin signaling and Ism1-mediated phosphoproteome-wide alterations in ~450 proteins that are not shared with insulin. Interestingly, we find several unknown phosphorylation sites on proteins related to protein translation, mTOR pathway, and, unexpectedly, muscle function in the Ism1 signaling network. Physiologically,

Indexed as

Muscle ProteinsProto-Oncogene Proteins c-aktAmino AcidsAnimalsGlucoseHypoglycemic AgentsInsulinIntercellular Signaling Peptides and ProteinsMechanistic Target of Rapamycin Complex 1MiceMuscle, SkeletalPhosphatidylinositol 3-KinasesProtein BiosynthesisTOR Serine-Threonine KinasesAmino AcidsGlucoseHypoglycemic AgentsInsulinIntercellular Signaling Peptides and Proteinsisthmin protein, mouseMechanistic Target of Rapamycin Complex 1Muscle ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinasescell biologymousemuscleproteomicssignaling

Identifiers

PMID36169399
PMCPMC9592085
OpenAlexW4297461745

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.