Evidence map›Paper›PMID 34073327›Full record

ArticleInternational journal of molecular sciences2021

Dual Stem Cell Therapy Improves the Myocardial Recovery Post-Infarction through Reciprocal Modulation of Cell Functions.

Sinziana Popescu, Mihai Bogdan Preda, Catalina Iolanda Marinescu, Maya Simionescu, Alexandrina Burlacu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Article
  8. Review
  9. Identification of CD141Stem cell research & therapy · 2024
    Article
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  18. Molecular Research in Cardiovascular Disease.International journal of molecular sciences · 2021
    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.

Sinziana PopescuInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 8, B.P. Hasdeu Street, 050568 Bucharest, Romania.
Mihai Bogdan PredaInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 8, B.P. Hasdeu Street, 050568 Bucharest, Romania.ORCID 0000-0003-2500-4078
Catalina Iolanda MarinescuInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 8, B.P. Hasdeu Street, 050568 Bucharest, Romania.ORCID 0000-0003-0727-3645
Maya SimionescuInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 8, B.P. Hasdeu Street, 050568 Bucharest, Romania.
Alexandrina BurlacuInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 8, B.P. Hasdeu Street, 050568 Bucharest, Romania.
Institute of Parasitology · CZ

Funding

Ministerul Educaţiei Naţionale PN-III-P4-ID-PCCF-2016-0172-contract no 05/18.07.2018Ministerul Educaţiei Naţionale PN-III-P4-ID-PCE-2020-1340-contract 122/2021Ministerul Educaţiei Naţionale PN-II-RU-TE-2014-4-1614-contract no 83/2015
6 · The paper itself

Abstract

Mesenchymal stromal cells (MSC) are promising candidates for regenerative therapy of the infarcted heart. However, poor cell retention within the transplantation site limits their potential. We hypothesized that MSC benefits could be enhanced through a dual-cell approach using jointly endothelial colony forming cells (ECFC) and MSC. To assess this, we comparatively evaluated the effects of the therapy with MSC and ECFC versus MSC-only in a mouse model of myocardial infarction. Heart function was assessed by echocardiography, and the molecular crosstalk between MSC and ECFC was evaluated in vitro through direct or indirect co-culture systems. We found that dual-cell therapy improved cardiac function in terms of ejection fraction and stroke volume. In vitro experiments showed that ECFC augmented MSC effector properties by increasing Connexin 43 and Integrin alpha-5 and the secretion of healing-associated molecules. Moreover, MSC prompted the organization of ECFC into vascular networks. This indicated a reciprocal modulation in the functionality of MSC and ECFC. In conclusion, the crosstalk between MSC and ECFC augments the therapeutic properties of MSC and enhances the angiogenic properties of ECFC. Our data consolidate the dual-cell therapy as a step forward for the development of effective treatments for patients affected by myocardial infarction.

Indexed as

Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationMyocardial InfarctionMyocardiumStroke VolumeAnimalsEndothelial Progenitor CellsFemaleHeterograftsMaleMiceMice, Inbred NODMice, SCIDdual stem cell therapyendothelial colony forming cellsmesenchymal stromal cellsmyocardial infarctionproteomic profiling

Identifiers

PMID34073327
PMCPMC8199446
OpenAlexW3164261055

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.