Evidence map›Paper›PMID 32130914›Full record

ArticleCell reports2020

Dynamic Interstitial Cell Response during Myocardial Infarction Predicts Resilience to Rupture in Genetically Diverse Mice.

Elvira Forte, Daniel A Skelly, Mandy Chen, Sandra Daigle, Kaesi A Morelli, Olivia Hon, Vivek M Philip, Mauro W Costa, Nadia A Rosenthal, Milena B Furtado

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 143 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
143citing papers in PubMed, 1 pooled it
19.0field-weighted citation impact, top 1% 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

143 citing papers in PubMed, 1 synthesis or guideline pooled it, 202 citations in OpenAlex.

  1. Myocardial Immune Cells: The Basis of Cardiac Immunology.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Pooled it
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  20. Integration of Bulk and Single-Cell RNA Sequencing Analyses in Biomedicine.International journal of molecular sciences · 2026
    Review

83 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 2 countries.

Elvira ForteThe Jackson Laboratory, Bar Harbor, ME 04609, USA. Electronic address: elvira.forte@jax.org.
Daniel A SkellyThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Mandy ChenThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Sandra DaigleThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Kaesi A MorelliThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Olivia HonThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Vivek M PhilipThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Mauro W CostaThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Nadia A RosenthalThe Jackson Laboratory, Bar Harbor, ME 04609, USA; National Heart and Lung Institute, Imperial College London, London SW72BX, UK.
Milena B FurtadoThe Jackson Laboratory, Bar Harbor, ME 04609, USA. Electronic address: mfurtado@amgen.com.
Jackson Laboratory · USLung Institute · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
British Heart FoundationNCI NIH HHS P30 CA034196
6 · The paper itself

Abstract

Cardiac ischemia leads to the loss of myocardial tissue and the activation of a repair process that culminates in the formation of a scar whose structural characteristics dictate propensity to favorable healing or detrimental cardiac wall rupture. To elucidate the cellular processes underlying scar formation, here we perform unbiased single-cell mRNA sequencing of interstitial cells isolated from infarcted mouse hearts carrying a genetic tracer that labels epicardial-derived cells. Sixteen interstitial cell clusters are revealed, five of which were of epicardial origin. Focusing on stromal cells, we define 11 sub-clusters, including diverse cell states of epicardial- and endocardial-derived fibroblasts. Comparing transcript profiles from post-infarction hearts in C57BL/6J and 129S1/SvImJ inbred mice, which displays a marked divergence in the frequency of cardiac rupture, uncovers an early increase in activated myofibroblasts, enhanced collagen deposition, and persistent acute phase response in 129S1/SvImJ mouse hearts, defining a crucial time window of pathological remodeling that predicts disease outcome.

Indexed as

AnimalsCicatrixHomeostasisMiceMice, Inbred StrainsMyocardial InfarctionMyocardiumMyofibroblastsPericardiumPhenotypeRNA-SeqRuptureSingle-Cell AnalysisStromal Cellscardiac ruptureepicardial-derivedfibrosisgenetic diversityheartmousemyocardial infarctionscRNAseqSeuratsingle-cell biology

Identifiers

PMID32130914
PMCPMC7059115
OpenAlexW3009508101

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.