Evidence map›Paper›PMID 33539327›Full record

ArticleJCI insight2021

Adipocyte-derived extracellular vesicles regulate survival and function of pancreatic β cells.

Iacopo Gesmundo, Barbara Pardini, Eleonora Gargantini, Giacomo Gamba, Giovanni Birolo, Alessandro Fanciulli, Dana Banfi, Noemi Congiusta, Enrica Favaro, Maria Chiara Deregibus and 17 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

79 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
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  5. Investigating Dietary microRNA Stability and Function Using a Transgenic Milk Model With Unique microRNA Sequences.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  16. Emerging role of exosomal-microRNA in obesity.Current opinion in physiology · 2025
    Article
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  18. Review
  19. Article
  20. Review

19 more citing papers are in PubMed but not listed here.

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

27 authors at 7 institutions in 5 countries.

Iacopo GesmundoDivision of Endocrinology, Diabetes and Metabolism, and.
Barbara PardiniItalian Institute for Genomic Medicine, Turin, Italy.
Eleonora GargantiniDivision of Endocrinology, Diabetes and Metabolism, and.
Giacomo GambaDivision of Endocrinology, Diabetes and Metabolism, and.
Giovanni BiroloDepartment of Medical Sciences, University of Turin, Turin, Italy.
Alessandro FanciulliDivision of Endocrinology, Diabetes and Metabolism, and.
Dana BanfiDivision of Endocrinology, Diabetes and Metabolism, and.
Noemi CongiustaDivision of Endocrinology, Diabetes and Metabolism, and.
Enrica FavaroDepartment of Medical Sciences, University of Turin, Turin, Italy.
Maria Chiara Deregibus2i3T Business Incubator and Technology Transfer and.
Gabriele TogliattoDepartment of Medical Sciences, University of Turin, Turin, Italy.
Gaia ZocaroDepartment of Medical Sciences, University of Turin, Turin, Italy.
Maria Felice BrizziDepartment of Medical Sciences, University of Turin, Turin, Italy.
Raul M LuqueMaimonides Institute for Biomedical Research of Córdoba, Department of Cell Biology, Physiology and Immunology, University of Córdoba, and Reina Sofia University Hospital, Córdoba, Spain.
Justo P CastañoMaimonides Institute for Biomedical Research of Córdoba, Department of Cell Biology, Physiology and Immunology, University of Córdoba, and Reina Sofia University Hospital, Córdoba, Spain.
Maria Alessandra BocchiottiDepartment of Reconstructive and Aesthetic Plastic Surgery and.
Simone ArolfoDepartment of Surgical Sciences, University of Turin, Turin, Italy.
Stefania BrunoDepartment of Medical Sciences, University of Turin, Turin, Italy.
Rita NanoDiabetes Research Institute, IRCCS San Raffaele Scientific Institute, and Vita-Salute San Raffaele University, Milan, Italy.
Mario MorinoDepartment of Surgical Sciences, University of Turin, Turin, Italy.
Lorenzo PiemontiDiabetes Research Institute, IRCCS San Raffaele Scientific Institute, and Vita-Salute San Raffaele University, Milan, Italy.
Huy OngFaculty of Pharmacy, University of Montréal, Montréal, Québec, Canada.
Giuseppe MatulloDepartment of Medical Sciences, University of Turin, Turin, Italy.
Juan M Falcón-PérezExosomes Laboratory and.
Ezio GhigoDivision of Endocrinology, Diabetes and Metabolism, and.
Giovanni CamussiDepartment of Medical Sciences, University of Turin, Turin, Italy.
Riccarda GranataDivision of Endocrinology, Diabetes and Metabolism, and.
Diabetes Australia · AUUniversity of Turin · ITItalian institute for Genomic Medicine · ITInstituto Maimónides de Investigación Biomédica de Córdoba · ESVita-Salute San Raffaele University · ITIkerbasque · ESUniversité de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs) are implicated in the crosstalk between adipocytes and other metabolic organs, and an altered biological cargo has been observed in EVs from human obese adipose tissue (AT). Yet, the role of adipocyte-derived EVs in pancreatic β cells remains to be determined. Here, we explored the effects of EVs released from adipocytes isolated from both rodents and humans and human AT explants on survival and function of pancreatic β cells and human pancreatic islets. EVs from healthy 3T3-L1 adipocytes increased survival and proliferation and promoted insulin secretion in INS-1E β cells and human pancreatic islets, both those untreated or exposed to cytokines or glucolipotoxicity, whereas EVs from inflamed adipocytes caused β cell death and dysfunction. Human lean adipocyte-derived EVs produced similar beneficial effects, whereas EVs from obese AT explants were harmful for human EndoC-βH3 β cells. We observed differential expression of miRNAs in EVs from healthy and inflamed adipocytes, as well as alteration in signaling pathways and expression of β cell genes, adipokines, and cytokines in recipient β cells. These in vitro results suggest that, depending on the physiopathological state of AT, adipocyte-derived EVs may influence β cell fate and function.

Indexed as

AdipocytesAdipose TissueIslets of Langerhans3T3-L1 CellsAdultAnimalsExtracellular VesiclesFemaleHumansMaleMiceObesityAdipose tissueBeta cellsDiabetesMetabolism

Identifiers

PMID33539327
PMCPMC8021102
OpenAlexW3127295600

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.