Evidence map›Paper›PMID 38600839›Full record

ArticleCurrent protocols2024

In Vitro Assessment of Cardiac Fibroblast Activation at Physiologic Stiffness.

Robert S Goldsmith, Yao-Chang Tsan, Rachel E Scissors, Adam S Helms, Matthew J Brody

Open access · hybridAbstract read
In one paragraph

Article in Current protocols, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Frontiers in cardiovascular medicine · 2026
    Article
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

5 authors at 1 institution in 1 country.

Robert S GoldsmithDepartment of Pharmacology, University of Michigan, Ann Arbor, Michigan.ORCID https://orcid.org/0000-0001-8292-6330
Yao-Chang TsanDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.ORCID https://orcid.org/0000-0003-4904-7670
Rachel E ScissorsDepartment of Pharmacology, University of Michigan, Ann Arbor, Michigan.
Adam S HelmsDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Matthew J BrodyDepartment of Pharmacology, University of Michigan, Ann Arbor, Michigan.
University of Michigan · US

Funding

S-acylation-dependent regulation of cytokine receptor signaling and cardiac maladaptationR01HL166274 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Matthew Jacob Brody · 2023 to 2026
$1.9M
The role of palmitoylation in cardiac signal transduction and disease pathogenesisR00HL136695 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BRODY, MATTHEW JACOB · 2019 to 2021
$747k
NHLBI NIH HHS R00 HL136695NHLBI NIH HHS R01 HL166274
6 · The paper itself

Abstract

Cardiac fibroblasts (CF) are an essential cell type in cardiac physiology, playing diverse roles in maintaining structural integrity, extracellular matrix (ECM) synthesis, and tissue repair. Under normal conditions, these cells reside in the interstitium in a quiescent state poised to sense and respond to injury by synthesizing and secreting collagen, vimentin, hyaluronan, and other ECM components. In response to mechanical and chemical stimuli, these "resident" fibroblasts can undergo a transformation through a continuum of activation states into what is commonly known as a "myofibroblast," in a process critical for injury response. Despite progress in understanding the contribution of fibroblasts to cardiac health and disease, much remains unknown about the signaling mediating this activation, in part owing to technical challenges in evaluating CF function and activation status in vitro. Given their role in monitoring the ECM, CFs are acutely sensitive to stiffness and pressure. High basal activation of isolated CFs is common due to the super-physiologic stiffness of traditional cell culture substrates, making assays dependent on quiescent cells challenging. To overcome this problem, cell culture parameters must be tightly controlled, and the use of dishes coated with biocompatible reduced-stiffness substrates, such as 8-kPa polydimethylsiloxane (PDMS), has shown promise in reducing basal activation of fibroblasts. Here, we describe cell culture protocol for maintaining CF quiescence in vitro to enable a dynamic range for the assessment of activation status in response to fibrogenic stimuli using PDMS-coated coverslips. Our protocol provides a cost-effective tool to study fibroblast signaling and activity, allowing researchers to better understand the underlying mechanisms involved in cardiac fibrosis. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Generation of 8-kPa polydimethylsiloxane (PDMS)/gelatin-coated coverslips for cardiac fibroblast cell culture Basic Protocol 2: Isolation of adult cardiac fibroblasts and plating onto PDMS coverslips Basic Protocol 3: Assessment of cardiac fibroblast activation by α smooth muscle actin (αSMA) immunocytochemistry.

Indexed as

FibroblastsHeartDimethylpolysiloxanesMyofibroblastsSignal TransductionDimethylpolysiloxanesactivationcardiac fibroblastscell culturefibrosismyofibroblastPDMSTGFβ

Identifiers

PMID38600839
PMCPMC11013569
OpenAlexW4394725100

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.