Evidence map›Paper›PMID 36967241›Full record

ArticlePhysiological reports2023

Visualization of cardiac uptake of bone marrow mesenchymal stem cell-derived extracellular vesicles after intramyocardial or intravenous injection in murine myocardial infarction.

Cynthia M Xu, Sharif A Sabe, Rayane Brinck-Teixeira, Mohamed Sabra, Frank W Sellke, M Ruhul Abid

Open access · goldFull text read
In one paragraph

Article in Physiological reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.9field-weighted citation impact, top 9% 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, 19 citations in OpenAlex.

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  11. Lab-grown, 3D extracellular matrix particles improve cardiac function and morphology in myocardial ischemia.American journal of physiology. Heart and circulatory physiology · 2025
    Article
  12. Mesenchymal stem cell therapy for pulmonary hypertension: an update.Frontiers in bioengineering and biotechnology · 2025
    Review
  13. Article
  14. Cardioprotection in cardiovascular surgery.Basic research in cardiology · 2024
    Review
  15. Article
  16. Review
  17. Article
  18. 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

6 authors at 1 institution in 1 country.

Cynthia M XuCardiovascular Research Center, Rhode Island Hospital, Providence, Rhode Island, USA.ORCID 0000-0002-2191-3066
Sharif A SabeCardiovascular Research Center, Rhode Island Hospital, Providence, Rhode Island, USA.
Rayane Brinck-TeixeiraCardiovascular Research Center, Rhode Island Hospital, Providence, Rhode Island, USA.
Mohamed SabraCardiovascular Research Center, Rhode Island Hospital, Providence, Rhode Island, USA.
Frank W SellkeCardiovascular Research Center, Rhode Island Hospital, Providence, Rhode Island, USA.
M Ruhul AbidCardiovascular Research Center, Rhode Island Hospital, Providence, Rhode Island, USA.ORCID 0000-0003-2981-2638
Providence College · US

Funding

Effect of Cardioplegia and Cardiopulmonary Bypass on Coronary Microvascular ReactivityR01HL046716 · NHLBI · RHODE ISLAND HOSPITAL · PI SELLKE, FRANK W · 1997 to 2023
$8.5M
Vascular Dysfunction in Myocardial Ischemia and Metabolic SyndromeR01HL128831 · NHLBI · RHODE ISLAND HOSPITAL · PI SELLKE, FRANK W, USHEVA-SIMIDJIYSKA, ANNY · 2016 to 2025
$5.7M
Trauma and Inflammation Research TrainingT32GM065085 · NIGMS · RHODE ISLAND HOSPITAL · PI Alfred Ayala · 2004 to 2026
$3.2M
Sub-cellular Targeting of Endothelial ROS in Myocardial IschemiaR01HL133624 · NHLBI · RHODE ISLAND HOSPITAL · PI ABID, RUHUL · 2017 to 2020
$1.6M
Cardiovascular Surgery Research Training GrantT32HL076130 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SELLKE, FRANK W · 2004 to 2008
$941k
Sub-cellular Targeting of Endothelial ROS in Myocardial IschemiaR56HL133624 · NHLBI · RHODE ISLAND HOSPITAL · PI ABID, RUHUL · 2022 to 2022
$613k
NHLBI NIH HHS 1R01HL133624NHLBI NIH HHS 2R56HL133624-05NHLBI NIH HHS R01 HL128831NHLBI NIH HHS R01HL128831-01A1NHLBI NIH HHS R01 HL133624NHLBI NIH HHS R01HL46716NHLBI NIH HHS R56 HL133624NIGMS NIH HHS T32 GM065085NIH HHS T32 GM065085-10
6 · The paper itself

Abstract

In animal models, human bone marrow mesenchymal stem cell-derived extracellular vesicles (MSC-EV) have been found to have beneficial effects in cardiovascular disease, but only when administered via intramyocardial injection. The biodistribution of either intravenous or intramyocardial injection of MSC-EV in the presence of myocardial injury is uncharacterized at this time. We hypothesized that intramyocardial injection will ensure delivery of MSC-EV to the ischemic myocardium, while intravenous injection will not. Human bone marrow mesenchymal stem cells were cultured and the MSC-EV were isolated and characterized. The MSC-EVs were then labeled with DiD lipid dye. FVB mice with normal cardiac function underwent left coronary artery ligation followed by either peri-infarct intramyocardial or tail vein injection of 3*10

Indexed as

Extracellular VesiclesMesenchymal Stem CellsMyocardial InfarctionAnimalsDisease Models, AnimalHumansInjections, IntravenousMiceTissue Distribution

Identifiers

PMID36967241
PMCPMC10040402
OpenAlexW4360981412

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read28
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.