Evidence map›Paper›PMID 19570514›Full record

ArticleCell stem cell2009

Intravenous hMSCs improve myocardial infarction in mice because cells embolized in lung are activated to secrete the anti-inflammatory protein TSG-6.

Ryang Hwa Lee, Andrey A Pulin, Min Jeong Seo, Daniel J Kota, Joni Ylostalo, Benjamin L Larson, Laura Semprun-Prieto, Patrice Delafontaine, Darwin J Prockop

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04093336 (Effect of Human Umbilical Cord Mesenchymal Stem Cells), which is not on this map. Cited by 1,041 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,041citing papers in PubMed, 3 pooled it
36.8field-weighted citation impact, top 1% 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.

NCT04093336 phase1 / phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

Effect of Human Umbilical Cord Mesenchymal Stem Cells(MSCs) Transplantation for on Prognosis of Acute Cerebral Infarction Patients

TypeinterventionalSponsorShanghai East HospitalRan2019 to 2024Enrolled120ConditionsInfarction, Middle Cerebral Artery, Infarction, Anterior Cerebral Artery, Cerebral Infarction, Stroke, IschemicArmshuman umbilical cord mesenchymal stem cells, Placebo, standardized treatment
3 · Its place in the literature

Who cites it

1,041 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,918 citations in OpenAlex.

  1. Pooled it
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  7. The hydrocup: a hollow electrospun scaffold forbioRxiv : the preprint server for biology · 2026
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  14. Reconceptualizing Aplastic Anemia-Seed, Worm, Soil.Journal of clinical laboratory analysis · 2026
    Review
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981 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Ryang Hwa LeeCenter for Gene Therapy, Tulane University Health Sciences Center, New Orleans, LA 70112, USA.
Andrey A Pulin
Min Jeong Seo
Daniel J Kota
Joni Ylostalo
Benjamin L Larson
Laura Semprun-Prieto
Patrice Delafontaine
Darwin J Prockop
Tulane University · USScott & White Memorial Hospital · USTexas A&M Health Science Center · US

Funding

Marrow Stromal Cell Homing to the Lung in EmphysemaP01HL075161 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI PHINNEY, DONALD G · 2005 to 2009
$9.1M
PREPARATION AND DISTRUBUTION OF ADULT STEM CELLS: HUMAN &RODENTP40RR017447 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI PROCKOP, DARWIN JOHNSON · 2003 to 2011
$8.9M
ANGIOTENSIN II, IGF-1 AND SKELETAL MUSCLE ATROPHYR01HL080682 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI DELAFONTAINE, PATRICE · 2007 to 2015
$3.3M
Culture and Lung Engraftment of Mesenchymal Stem CellsR01HL073252 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI PROCKOP, DARWIN JOHNSON · 2003 to 2006
$1.8M
NCRR NIH HHS P40 RR017447NCRR NIH HHS P40 RR 17447NHLBI NIH HHS 1R01HL080682-01A2NHLBI NIH HHS HL073252NHLBI NIH HHS P01 HL 075161NHLBI NIH HHS P01 HL075161NHLBI NIH HHS R01 HL073252NHLBI NIH HHS R01 HL080682
6 · The paper itself

Abstract

Quantitative assays for human DNA and mRNA were used to examine the paradox that intravenously (i.v.) infused human multipotent stromal cells (hMSCs) can enhance tissue repair without significant engraftment. After 2 x 10(6) hMSCs were i.v. infused into mice, most of the cells were trapped as emboli in lung. The cells in lung disappeared with a half-life of about 24 hr, but <1000 cells appeared in six other tissues. The hMSCs in lung upregulated expression of multiple genes, with a large increase in the anti-inflammatory protein TSG-6. After myocardial infarction, i.v. hMSCs, but not hMSCs transduced with TSG-6 siRNA, decreased inflammatory responses, reduced infarct size, and improved cardiac function. I.v. administration of recombinant TSG-6 also reduced inflammatory responses and reduced infarct size. The results suggest that improvements in animal models and patients after i.v. infusions of MSCs are at least in part explained by activation of MSCs to secrete TSG-6.

Indexed as

AnimalsCell Adhesion MoleculesCell Migration AssaysGene Expression ProfilingHeartHumansInflammation MediatorsInfusions, IntravenousLungMiceMultipotent Stem CellsMyocardial InfarctionPulmonary EmbolismStromal CellsCell Adhesion MoleculesInflammation MediatorsTnfaip6 protein, mouse

Identifiers

PMID19570514
PMCPMC4154377
OpenAlexW2021916724

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.