Evidence map›Paper›PMID 32670081›Full record

ArticleFrontiers in physiology2020

Human Cardiac Mesenchymal Stromal Cells From Right and Left Ventricles Display Differences in Number, Function, and Transcriptomic Profile.

Ilaria Stadiotti, Luca Piacentini, Chiara Vavassori, Mattia Chiesa, Alessandro Scopece, Anna Guarino, Barbara Micheli, Gianluca Polvani, Gualtiero Ivanoe Colombo, Giulio Pompilio and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Ilaria StadiottiUnit of Vascular Biology and Regenerative Medicine, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Luca PiacentiniUnit of Immunology and Functional Genomics, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Chiara VavassoriUnit of Immunology and Functional Genomics, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Mattia ChiesaUnit of Immunology and Functional Genomics, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Alessandro ScopeceUnit of Vascular Biology and Regenerative Medicine, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Anna GuarinoCardiovascular Tissue Bank, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Barbara MicheliCardiovascular Tissue Bank, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Gianluca PolvaniCardiovascular Tissue Bank, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Gualtiero Ivanoe ColomboUnit of Immunology and Functional Genomics, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Giulio PompilioUnit of Vascular Biology and Regenerative Medicine, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Elena SommarivaUnit of Vascular Biology and Regenerative Medicine, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Centro Cardiologico Monzino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeft ventricle (LV) and right ventricle (RV) are characterized by well-known physiological differences, mainly related to their different embryological origin, hemodynamic environment, function, structure, and cellular composition. Nevertheless, scarce information is available about cellular peculiarities between left and right ventricular chambers in physiological and pathological contexts. Cardiac mesenchymal stromal cells (C-MSC) are key cells affecting many functions of the heart. Differential features that distinguish LV from RV C-MSC are still underappreciated.

aimTo analyze the physiological differential amount, function, and transcriptome of human C-MSC in LV versus (vs.) RV.

methodsHuman cardiac specimens of LV and RV from healthy donors were used for tissue analysis of C-MSC number, and for C-MSC isolation. Paired LV and RV C-MSC were compared as for surface marker expression, cell proliferation/death ratio, migration, differentiation capabilities, and transcriptome profile.

resultsHistological analysis showed a greater percentage of C-MSC in RV vs. LV tissue. Moreover, a higher C-MSC amount was obtained from RV than from LV after isolation procedures. LV and RV C-MSC are characterized by a similar proportion of surface markers. Functional studies revealed comparable cell growth curves in cells from both ventricles. Conversely, LV C-MSC displayed a higher apoptosis rate and RV C-MSC were characterized by a higher migration speed and collagen deposition. Consistently, transcriptome analysis showed that genes related to apoptosis regulation or extracellular matrix organization and integrins were over-expressed in LV and RV, respectively. Besides, we revealed additional pathways specifically associated with LV or RV C-MSC, including energy metabolism, inflammatory response, cardiac conduction, and pluripotency.

conclusionTaken together, these results contribute to the functional characterization of RV and LV C-MSC in physiological conditions. This information suggests a possible differential role of the stromal compartment in chamber-specific pathologic scenarios.

Indexed as

cardiac mesenchymal stromal cellscardiac ventriclesfunctional studiesleft ventricleright ventricletranscriptome

Identifiers

PMID32670081
PMCPMC7327120
OpenAlexW3036220582

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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.