Evidence map›Paper›PMID 40162230›Full record

ArticleResearch square2025

TGFβ-activated kinase 1 signaling controls acquisition of the inflammatory fibroblast phenotype and regulates cardiac remodeling after myocardial infarction.

Daniel C Nguyen, Jonah K Stephan, Robert E Brainard, Kenneth R Brittian, Lianay Gutierrez Luque, Collin K Wells, Madison S Taylor, Yania Martinez-Ondaro, Kara R Gouwens, Danielle T Little and 5 more

Abstract readPreprint
In one paragraph

Article in Research square, 2025. 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

15 authors.

Daniel C NguyenCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Jonah K StephanCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.ORCID 0000-0002-8957-1277
Robert E BrainardDepartment of Physiology, University of Louisville, Louisville, KY.
Kenneth R BrittianCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Lianay Gutierrez LuqueCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Collin K WellsCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.ORCID 0000-0002-8497-2848
Madison S TaylorCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Yania Martinez-OndaroCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Kara R GouwensCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Danielle T LittleCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Nolan BoydCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.ORCID 0000-0001-9537-6040
Richa A SinghalCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Jason HellmannCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Marcin WysoczynskiCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.
Bradford G HillCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, School of Medicine, University of Louisville, Louisville, KY.ORCID 0000-0001-5332-8286

Funding

TBDP30GM127607 · NIGMS · UNIVERSITY OF LOUISVILLE · PI BHATNAGAR, ARUNI · 2018 to 2022
$6.3M
Biosynthetic Pathways in Cardiac RemodelingR01HL147844 · NHLBI · UNIVERSITY OF LOUISVILLE · PI HILL, BRADFORD GUY, JONES, STEVEN P · 2019 to 2022
$3.0M
Role of the PEP cycle in cardiac fibrosisR01HL168198 · NHLBI · UNIVERSITY OF LOUISVILLE · PI Bradford Guy Hill · 2024 to 2026
$1.7M
Imaging and Physiology Core: High Frequency, High Resolution Ultrasound Imaging SystemS10OD025178 · OD · UNIVERSITY OF LOUISVILLE · PI JONES, STEVEN P · 2019 to 2019
$364k
Fibroblast TAK1 signaling in cardiac fibrosisF30HL165813 · NHLBI · UNIVERSITY OF LOUISVILLE · PI Daniel Nguyen · 2023 to 2026
$163k
Role of Pck2 in cardiac fibrosisF31HL165826 · NHLBI · UNIVERSITY OF LOUISVILLE · PI WELLS, COLLIN · 2022 to 2025
$141k
NHLBI NIH HHS F30 HL165813NHLBI NIH HHS F31 HL165826NHLBI NIH HHS R01 HL147844NHLBI NIH HHS R01 HL168198NIGMS NIH HHS P30 GM127607NIH HHS S10 OD025178
6 · The paper itself

Abstract

Organ health and function depend on communication between cell types to coordinate tissue growth and repair. Recent studies have indicated that fibroblasts are critical to this process; however, their role in regulating inflammatory responses to injury have remained ambiguous. Here, we demonstrate that transforming growth factor β-activated kinase 1 (TAK1) is a gatekeeper of the inflammatory cardiac fibroblast phenotype. We find that TAK1 propagates IL-1β and TNF-α signaling in cardiac fibroblasts and coordinates the synthesis and secretion of chemokines as well as inflammatory and pro-resolving lipid mediators. Deletion of TAK1 in fibroblasts decreased immune cell recruitment after MI, which was associated with improved cardiac structural and functional remodeling in male mice. Nevertheless, we found the effects of TAK1 deletion to be sexually dimorphic in nature, providing support to the idea that the protected phenotype of the female sex may be based in disparate immune and inflammatory responses. Moreover, TAK1 signaling controlled the acquisition of novel markers of the inflammatory fibroblast phenotype, having a biological basis in redox stress, chemokine and lipid mediator biosynthesis, metalloproteinase activity, and damage-associated molecular pattern recognition. Collectively, these results further resolve the nature and function of inflammatory cardiac fibroblasts in cardiac responses to injury and identify TAK1 signaling in fibroblasts as a potential target for therapy.

Identifiers

PMID40162230
PMCPMC11952645

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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.