Evidence map›Paper›PMID 31109997›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Multipotent fetal-derived Cdx2 cells from placenta regenerate the heart.

Sangeetha Vadakke-Madathil, Gina LaRocca, Koen Raedschelders, Jesse Yoon, Sarah J Parker, Joseph Tripodi, Vesna Najfeld, Jennifer E Van Eyk, Hina W Chaudhry

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Presence of fetal microchimerisms in the heart and effect on cardiac repair.Frontiers in cell and developmental biology · 2024
    Article
  8. Article
  9. Regulation of maternal-fetal metabolic communication.Cellular and molecular life sciences : CMLS · 2021
    Review
  10. Article
  11. Review
  12. Multipotency of mouse trophoblast stem cells.Stem cell research & therapy · 2020
    Article
  13. Article
  14. Recent advances in myocardial regeneration strategy.The Journal of international medical research · 2019
    Review
  15. Placental stem cells can regenerate the heart.Nature reviews. Cardiology · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Sangeetha Vadakke-MadathilCardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Gina LaRoccaCardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Koen RaedscheldersAdvanced Clinical Biosystems Research Institute, Smidt Heart Institute, Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048.
Jesse YoonCardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Sarah J ParkerAdvanced Clinical Biosystems Research Institute, Smidt Heart Institute, Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048.
Joseph TripodiCardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Vesna NajfeldCardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Jennifer E Van EykAdvanced Clinical Biosystems Research Institute, Smidt Heart Institute, Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048.
Hina W ChaudhryCardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029; hina.chaudhry@mssm.edu.
Icahn School of Medicine at Mount Sinai · USCedars-Sinai Medical Center · USCardiovascular Institute of the South · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extremely limited regenerative potential of adult mammalian hearts has prompted the need for novel cell-based therapies that can restore contractile function in heart disease. We have previously shown the regenerative potential of mixed fetal cells that were naturally found migrating to the injured maternal heart. Exploiting this intrinsic mechanism led to the current hypothesis that Caudal-type homeobox-2 (Cdx2) cells in placenta may represent a novel cell type for cardiac regeneration. Using a lineage-tracing strategy, we specifically labeled fetal-derived Cdx2 cells with enhanced green fluorescent protein (eGFP). Cdx2-eGFP cells from end-gestation placenta were assayed for cardiac differentiation in vitro and in vivo using a mouse model of myocardial infarction. We observed that these cells differentiated into spontaneously beating cardiomyocytes (CMs) and vascular cells in vitro, indicating multipotentiality. When administered via tail vein to infarcted wild-type male mice, they selectively and robustly homed to the heart and differentiated to CMs and blood vessels, resulting in significant improvement in contractility as noted by MRI. Proteomics and immune transcriptomics studies of Cdx2-eGFP cells compared with embryonic stem (ES) cells reveal that they appear to retain "stem"-related functions of ES cells but exhibit unique signatures supporting roles in homing and survival, with an ability to evade immune surveillance, which is critical for cell-based therapy. Cdx2-eGFP cells may potentially represent a therapeutic advance in allogeneic cell therapy for cardiac repair.

Indexed as

AnimalsCDX2 Transcription FactorCell DifferentiationCells, CulturedEmbryonic Stem CellsFemaleFetusGreen Fluorescent ProteinsHeartHeart DiseasesMaleMiceMice, Inbred C57BLMultipotent Stem CellsMyocardial InfarctionMyocytes, CardiacCdx2 protein, mouseCDX2 Transcription Factorenhanced green fluorescent proteinGreen Fluorescent Proteinscardiac regenerationcardiomyocytesCdx2placentastem cells

Identifiers

PMID31109997
PMCPMC6576083
OpenAlexW2945666534

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.