Evidence map›Paper›PMID 41453954›Full record

ArticleScientific reports2025

Trimethylamine-N-oxide promotes fibrotic activation of quiescent valvular interstitial cells via endoplasmic reticulum stress.

Samanvitha Sudi, Sai Drishya Suresh, Tanmayee Kolli, Karen Mancera Azamar, Aniyah Dickson, Zahra Mohammadalizadeh, Ana Maria Porras

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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

7 authors.

Samanvitha SudiJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA.
Sai Drishya SureshJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA.
Tanmayee KolliJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA.
Karen Mancera AzamarJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA.
Aniyah DicksonJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA.
Zahra MohammadalizadehJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA.
Ana Maria PorrasJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA. anaporras@ufl.edu.

Funding

BASIC MICROBIOLOGY &INFECTIOUS DISEASEST32AI007110 · NIAID · UNIVERSITY OF FLORIDA · PI Stephanie M Karst · 1985 to 2026
$4.3M
Microbiota and Extracellular Matrix Interactions that Drive Host Tissue RemodelingR35GM155229 · NIGMS · UNIVERSITY OF FLORIDA · PI Ana Maria Porras · 2024 to 2026
$1.1M
NIAID NIH HHS T32 AI007110NIGMS NIH HHS R35 GM155229NIH HHS R35GM155229NIH HHS T32 AI007110
6 · The paper itself

Abstract

Calcific aortic valve disease currently lacks effective treatments beyond aortic valve replacement, largely due to an incomplete understanding of its pathogenesis. Emerging evidence suggests that the gut microbiome influences cardiovascular health through the production of metabolites derived from dietary components. Among these metabolites, trimethylamine-N-oxide (TMAO) has been identified as a potential causal factor for several cardiovascular conditions. However, its specific role in the development of aortic valve disease remains poorly understood. This study sought to investigate the impact of TMAO on valvular interstitial cells (VICs), the most abundant cell type in the aortic valve. Here, we demonstrate that TMAO activates aortic VICs towards a myofibroblastic phenotype through the induction of endoplasmic reticulum stress. Using a novel in vitro protocol to generate quiescent VICs, we found that TMAO induces the upregulation of the myofibroblastic proteins α-smooth muscle actin and transgelin in a sex-independent manner. These quiescent VICs were more sensitive to TMAO than conventionally cultured VICs. Treatment with TMAO also elevated extracellular matrix production and oxidative stress, phenotypic hallmarks of an activated profibrotic state. Finally, inhibition of the endoplasmic reticulum stress kinase prior to TMAO treatment blocked all effects of this metabolite on VIC phenotype. These findings suggest that TMAO contributes to the early stages of valve disease by promoting VIC activation and extracellular matrix production through endoplasmic reticulum stress mechanisms. Understanding the role of TMAO and other gut-derived metabolites in the pathogenesis of valve disease could inform the development of novel preventive or therapeutic strategies to modify or delay disease progression. Furthermore, these insights underscore the importance of host-microbiome interactions for cardiovascular health and highlight the potential for targeted dietary interventions to mitigate disease risk.

Indexed as

Aortic ValveAortic Valve StenosisEndoplasmic Reticulum StressMethylaminesAnimalsCalcinosisCells, CulturedExtracellular MatrixFemaleFibrosisHumansMaleMyofibroblastsOxidative StressMethylaminestrimethyloxamineAortic valve diseaseER stressGut microbiomeMatrix biologyMetabolitesTMAOValvular interstitial cells

Identifiers

PMID41453954
PMCPMC12816747

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LicenceCC BY-NC-ND
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Registered trials

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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.