Evidence map›Paper›PMID 36473871›Full record

ArticleNature communications2022

The dynamic clustering of insulin receptor underlies its signaling and is disrupted in insulin resistance.

Alessandra Dall'Agnese, Jesse M Platt, Ming M Zheng, Max Friesen, Giuseppe Dall'Agnese, Alyssa M Blaise, Jessica B Spinelli, Jonathan E Henninger, Erin N Tevonian, Nancy M Hannett and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
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  6. Article
  7. Article
  8. ThePharmaceuticals (Basel, Switzerland) · 2025
    Article
  9. Molecular Framework of the Onset and Progression of Skeletal Muscle Aging.International journal of molecular sciences · 2025
    Review
  10. Review
  11. The insulin signalling network.Nature metabolism · 2025
    Review
  12. Article
  13. Advanced optical microscopy methods forBiophysical reviews · 2025
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Protein interactions, calcium, phosphorylation, and cholesterol modulate CFTR cluster formation on membranes.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Article
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

20 authors at 4 institutions in 2 countries.

Alessandra Dall'Agnese *Whitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.
Jesse M Platt *Whitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.
Ming M ZhengWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.
Max FriesenWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.ORCID 0000-0002-6699-6619
Giuseppe Dall'AgneseWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.
Alyssa M BlaiseWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.ORCID 0000-0001-9958-4488
Jessica B SpinelliWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.ORCID 0000-0003-3657-4578
Jonathan E HenningerWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.ORCID 0000-0002-9604-2007
Erin N TevonianDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Nancy M HannettWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.
Charalampos LazarisWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.ORCID 0000-0002-7345-8288
Hannah K DrescherDivision of Gastroenterology, Department of Medicine, Massachusetts General Hospital, Boston, MA, 02114, USA.
Lea M BartschDivision of Gastroenterology, Department of Medicine, Massachusetts General Hospital, Boston, MA, 02114, USA.
Henry R KilgoreWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.ORCID 0000-0003-4851-9656
Rudolf JaenischWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.ORCID 0000-0002-2540-7099
Linda G GriffithDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.ORCID 0000-0002-1801-5548
Ibrahim I CisseDepartment of Physics, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.ORCID 0000-0002-8764-1809
Jacob F JeppesenWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA.
Tong I LeeWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA. tlee@wi.mit.edu.ORCID 0000-0003-1847-0898
Richard A YoungWhitehead Institute for Biomedical Research, Cambridge, MA, 02142, USA. young@wi.mit.edu.ORCID 0000-0001-8855-8647
Whitehead Institute for Biomedical Research · USMassachusetts General Hospital · USMassachusetts Institute of Technology · USNovo Nordisk (Denmark) · DK

Funding

RESEARCH TRAINING IN DIGESTIVE DISEASES AND NUTRITIONT32DK007191 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1986 to 2026
$14.6M
Institutional Career Development CoreKL2TR002542 · NCATS · HARVARD MEDICAL SCHOOL · PI BREDELLA, MIRIAM ANTOINETTE, RUTKOVE, SEWARD B. · 2018 to 2022
$8.7M
Transcriptional regulation in mammalian cellsR35GM144283 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI RICHARD YOUNG · 2022 to 2026
$4.0M
Transcriptional regulatory networks in living cellsR01GM123511 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI YOUNG, RICHARD · 2017 to 2020
$3.6M
IMAGING TRANSCRIPTION WITH SINGLE MOLECULE RESOLUTION IN LIVE MAMMALIAN CELLSDP2CA195769 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI CISSE, IBRAHIM · 2014 to 2014
$2.3M
Zeiss LSM 980 with Airyscan 2 confocal microscope systemS10OD028520 · OD · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI CHEESEMAN, IAIN MCPHERSON · 2021 to 2021
$600k
RNA-mediated Feedback Control of Oncogenic TranscriptionF32CA254216 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI HENNINGER, JONATHAN EDWARD · 2020 to 2022
$206k
NCATS NIH HHS KL2 TR002542NCI NIH HHS DP2 CA195769NCI NIH HHS F32 CA254216NIDDK NIH HHS T32 DK007191NIGMS NIH HHS R01 GM123511NIGMS NIH HHS R35 GM144283NIH HHS S10 OD028520
6 · The paper itself

Abstract

Insulin receptor (IR) signaling is central to normal metabolic control and is dysregulated in metabolic diseases such as type 2 diabetes. We report here that IR is incorporated into dynamic clusters at the plasma membrane, in the cytoplasm and in the nucleus of human hepatocytes and adipocytes. Insulin stimulation promotes further incorporation of IR into these dynamic clusters in insulin-sensitive cells but not in insulin-resistant cells, where both IR accumulation and dynamic behavior are reduced. Treatment of insulin-resistant cells with metformin, a first-line drug used to treat type 2 diabetes, can rescue IR accumulation and the dynamic behavior of these clusters. This rescue is associated with metformin's role in reducing reactive oxygen species that interfere with normal dynamics. These results indicate that changes in the physico-mechanical features of IR clusters contribute to insulin resistance and have implications for improved therapeutic approaches.

Indexed as

Diabetes Mellitus, Type 2Insulin ResistanceHumansInsulinReceptor, InsulinInsulinReceptor, Insulin

Identifiers

PMID36473871
PMCPMC9727033
OpenAlexW4311589400

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.