Evidence map›Paper›PMID 32098400›Full record

ArticleCells2020

RNA-Based Strategies for Cardiac Reprogramming of Human Mesenchymal Stromal Cells.

Paula Mueller, Markus Wolfien, Katharina Ekat, Cajetan Immanuel Lang, Dirk Koczan, Olaf Wolkenhauer, Olga Hahn, Kirsten Peters, Hermann Lang, Robert David and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Brachyury engineers cardiac repair competent stem cells.Stem cells translational medicine · 2021
    Article
  7. A preview of selected articles.Stem cells translational medicine · 2021
    Article
  8. Review
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 2 institutions in 2 countries.

Paula MuellerDepartment of Cardiac Surgery, Reference and Translation Center for Cardiac Stem Cell Therapy (RTC), Rostock University Medical Center, 18057 Rostock, Germany.
Markus WolfienInstitute of Computer Science, Department of Systems Biology and Bioinformatics, University of Rostock, 18057 Rostock, Germany.ORCID 0000-0002-1887-4772
Katharina EkatDepartment of Cell Biology, Rostock University Medical Center, 18057 Rostock, Germany.
Cajetan Immanuel LangDepartment of Cardiology, Rostock University Medical Center, 18057 Rostock, Germany.
Dirk KoczanInstitute of Immunology, Rostock University Medical Center, 18057 Rostock, Germany.
Olaf WolkenhauerInstitute of Computer Science, Department of Systems Biology and Bioinformatics, University of Rostock, 18057 Rostock, Germany.
Olga HahnDepartment of Cell Biology, Rostock University Medical Center, 18057 Rostock, Germany.
Kirsten PetersDepartment of Cell Biology, Rostock University Medical Center, 18057 Rostock, Germany.ORCID 0000-0003-0254-176X
Hermann LangDepartment of Operative Dentistry and Periodontology, Rostock University Medical Center, 18057 Rostock, Germany.
Robert DavidDepartment of Cardiac Surgery, Reference and Translation Center for Cardiac Stem Cell Therapy (RTC), Rostock University Medical Center, 18057 Rostock, Germany.
Heiko LemckeDepartment of Cardiac Surgery, Reference and Translation Center for Cardiac Stem Cell Therapy (RTC), Rostock University Medical Center, 18057 Rostock, Germany.
University of Rostock · DEStellenbosch University · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multipotent adult mesenchymal stromal cells (MSCs) could represent an elegant source for the generation of patient-specific cardiomyocytes needed for regenerative medicine, cardiovascular research, and pharmacological studies. However, the differentiation of adult MSC into a cardiac lineage is challenging compared to embryonic stem cells or induced pluripotent stem cells. Here we used non-integrative methods, including microRNA and mRNA, for cardiac reprogramming of adult MSC derived from bone marrow, dental follicle, and adipose tissue. We found that MSC derived from adipose tissue can partly be reprogrammed into the cardiac lineage by transient overexpression of GATA4, TBX5, MEF2C, and MESP1, while cells isolated from bone marrow, and dental follicle exhibit only weak reprogramming efficiency. qRT-PCR and transcriptomic analysis revealed activation of a cardiac-specific gene program and up-regulation of genes known to promote cardiac development. Although we did not observe the formation of fully mature cardiomyocytes, our data suggests that adult MSC have the capability to acquire a cardiac-like phenotype when treated with mRNA coding for transcription factors that regulate heart development. Yet, further optimization of the reprogramming process is mandatory to increase the reprogramming efficiency.

Indexed as

Adipose TissueAdultBone Marrow CellsCell DifferentiationCell LineageCellular ReprogrammingCellular Reprogramming TechniquesDental SacGene Expression ProfilingHumansMesenchymal Stem CellsMicroRNAsMyocytes, CardiacReal-Time Polymerase Chain ReactionRNA, MessengerTranscription FactorsMicroRNAsRNA, MessengerTranscription Factorscardiac differentiationcardiac reprogrammingmesenchymal stromal cells (MSC)miRNAmRNA

Identifiers

PMID32098400
PMCPMC7072829
OpenAlexW3008020163

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.