Evidence map›Paper›PMID 35263542›Full record

ArticleJournal of proteome research2022

Messages from the Small Intestine Carried by Extracellular Vesicles in Prediabetes: A Proteomic Portrait.

Inês Ferreira, Rita Machado de Oliveira, Ana Sofia Carvalho, Akiko Teshima, Hans Christian Beck, Rune Matthiesen, Bruno Costa-Silva, Maria Paula Macedo

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Inês FerreiraChronic Diseases Research Centre, CEDOC, NOVA Medical School, (NMS/FCM), Lisbon 1169-056, Portugal.
Rita Machado de OliveiraChronic Diseases Research Centre, CEDOC, NOVA Medical School, (NMS/FCM), Lisbon 1169-056, Portugal.ORCID 0000-0002-0970-4501
Ana Sofia CarvalhoChronic Diseases Research Centre, CEDOC, NOVA Medical School, (NMS/FCM), Lisbon 1169-056, Portugal.
Akiko TeshimaChronic Diseases Research Centre, CEDOC, NOVA Medical School, (NMS/FCM), Lisbon 1169-056, Portugal.
Hans Christian BeckCentre for Clinical Proteomics, Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense 5000, Denmark.
Rune MatthiesenChronic Diseases Research Centre, CEDOC, NOVA Medical School, (NMS/FCM), Lisbon 1169-056, Portugal.ORCID 0000-0002-6353-2616
Bruno Costa-SilvaChampalimaud Research, Champalimaud Centre for the Unknown, 1400-038 Lisbon, Portugal.
Maria Paula MacedoChronic Diseases Research Centre, CEDOC, NOVA Medical School, (NMS/FCM), Lisbon 1169-056, Portugal.
Universidade Nova de Lisboa · PTChampalimaud Foundation · PTAssociacao Protectora dos Diabeticos de Portugal · PTOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EVs) mediate communication in physiological and pathological conditions. In the pathogenesis of type 2 diabetes, inter-organ communication plays an important role in its progress and metabolic surgery leads to its remission. Moreover, gut dysbiosis is emerging as a diabetogenic factor. However, it remains unclear how the gut senses metabolic alterations and whether this is transmitted to other tissues via EVs. Using a diet-induced prediabetic mouse model, we observed that protein packaging in gut-derived EVs (GDE), specifically the small intestine, is altered in prediabetes. Proteins related to lipid metabolism and to oxidative stress management were more abundant in prediabetic GDE compared to healthy controls. On the other hand, proteins related to glycolytic activity, as well as those responsible for the degradation of polyubiquitinated composites, were depleted in prediabetic GDE. Together, our findings show that protein packaging in GDE is markedly modified during prediabetes pathogenesis, thus suggesting that prediabetic alterations in the small intestine are translated into modified GDE proteomes, which are dispersed into the circulation where they can interact with and influence the metabolic status of other tissues. This study highlights the importance of the small intestine as a tissue that propagates prediabetic metabolic dysfunction throughout the body and the importance of GDE as the messengers. Data are available via ProteomeXchange with identifier PXD028338.

Indexed as

Diabetes Mellitus, Type 2Extracellular VesiclesPrediabetic StateAnimalsIntestine, SmallMiceProteomeProteomicsProteomedietextracellular vesicleslipidssmall intestinestype 2 diabetes

Identifiers

PMID35263542
PMCPMC8982452
OpenAlexW4221094286

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.