Evidence map›Paper›PMID 39574609›Full record

ArticlebioRxiv : the preprint server for biology2024

EXOSOMES FROM CYCLIC MICE MODULATE LIVER TRANSCRIPTOME IN ESTROUPAUSE MICE INDEPENDENT OF AGE.

Bianka M Zanini, Bianca M Ávila, Jéssica D Hense, Driele N Garcia, Sarah Ashiqueali, Pâmela I C Alves, Thais L Oliveira, Tiago V Collares, Miguel A Brieño-Enríquez, Jeffrey B Mason and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Bianka M ZaniniFaculdade de Nutrição, Universidade Federal de Pelotas, Pelotas - RS, Brazil.
Bianca M ÁvilaFaculdade de Nutrição, Universidade Federal de Pelotas, Pelotas - RS, Brazil.
Jéssica D HenseFaculdade de Nutrição, Universidade Federal de Pelotas, Pelotas - RS, Brazil.
Driele N GarciaFaculdade de Nutrição, Universidade Federal de Pelotas, Pelotas - RS, Brazil.
Sarah AshiquealiCollege of Medicine, Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, USA.
Pâmela I C AlvesPrograma de Pós-Graduação em Ciência e Tecnologia de Alimentos, Universidade Federal de Pelotas -RS, Brasil.
Thais L OliveiraCentro de Biotecnologia, Universidade Federal de Pelotas - RS, Brasil.
Tiago V CollaresCentro de Biotecnologia, Universidade Federal de Pelotas - RS, Brasil.
Miguel A Brieño-EnríquezDepartment of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Research Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Jeffrey B MasonCollege of Veterinary Medicine, Department of Veterinary Clinical and Life Sciences, Center for Integrated BioSystems, Utah State University, Logan, UT, USA.
Michal M MasternakUniversity of Central Florida, College of Medicine, Burnett School of Biomedical Sciences, Orlando, Florida, USA.
Augusto SchneiderFaculdade de Nutrição, Universidade Federal de Pelotas, Pelotas - RS, Brazil.ORCID 0000-0002-3410-2860

Funding

Ovarian derived exosomal miRNA as a juvenile protective factorsR56AG074499 · NIA · UNIVERSITY OF CENTRAL FLORIDA · PI MASTERNAK, MICHAL MATEUSZ · 2022 to 2022
$287k
NIA NIH HHS R56 AG074499
6 · The paper itself

Abstract

Background: Exosomes are extracellular vesicles secreted by cells that contain microRNAs (miRNAs). These miRNAs can induce changes in gene expression and function of recipient cells. In different cells exosome content can change with age and physiological state affecting tissues function and health. Aims: Therefore, the aim of this study was to characterize the miRNA content and role of exosomes from cyclic female mice in the modulation of liver transcriptome in estropausal mice. Main Methods: Two-month-old female mice were induced to estropause using 4-vinylcyclohexene diepoxide (VCD). At six months of age VCD-treated mice were divided in control group (VCD) and exosome treated group (VCD+EXO), which received 10 injections at 3-day intervals of exosomes extracted from serum of cyclic female mice (CTL). Key findings: Exosome injection in estropausal mice had no effect on body mass, insulin sensitivity or organ weight. We observed ten miRNAs differentially regulated in serum exosomes of VCD compared to CTL mice. In the liver we observed 931 genes differentially expressed in VCD+EXO compared to VCD mice. Interestingly, eight pathways were up-regulated in liver by VCD treatment and down-regulated by exosome treatment, indicating that exosomes from cyclic mice can reverse changes promoted by estropause in liver. Significance: Our findings indicate that miRNAs content in exosomes is regulated by estropause in mice independent of age. Additionally, treatment of estropausal mice with exosomes from cyclic mice can partially reverse changes in liver transcriptome.

Indexed as

menopausemiRNAsovarian agingVCD

Identifiers

PMID39574609
PMCPMC11580851

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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.