Evidence map›Paper›PMID 24551087›Full record

ArticlePloS one2014

Comparison of angiogenic, cytoprotective, and immunosuppressive properties of human amnion- and chorion-derived mesenchymal stem cells.

Kenichi Yamahara, Kazuhiko Harada, Makiko Ohshima, Shin Ishikane, Shunsuke Ohnishi, Hidetoshi Tsuda, Kentaro Otani, Akihiko Taguchi, Toshihiro Soma, Hiroyasu Ogawa and 5 more

Registry-linked trialOpen access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03440541 (Uses of Gamma Irradiated Amniotic Membrane as an Alternative Method in Psoriasis Treatment), which is not on this map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 3% 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.

NCT03440541 nacompletednot on this mapstarted 2015, after this paper: background citation

Uses of Gamma Irradiated Amniotic Membrane as an Alternative Method in Psoriasis Treatment

TypeinterventionalSponsorEgyptian Atomic Energy AuthorityRan2015 to 2016Enrolled22ConditionsPsoriasisArmsREGE pro
3 · Its place in the literature

Who cites it

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

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  15. Mesenchymal stem cells and their microenvironment.Stem cell research & therapy · 2022
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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

15 authors at 5 institutions in 1 country.

Kenichi YamaharaDepartment of Regenerative Medicine and Tissue Engineering, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Kazuhiko HaradaDepartment of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Makiko OhshimaDepartment of Regenerative Medicine and Tissue Engineering, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Shin IshikaneDepartment of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Shunsuke OhnishiDepartment of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Sapporo, Hokkaido, Japan.
Hidetoshi TsudaDepartment of Regenerative Medicine and Tissue Engineering, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Kentaro OtaniDepartment of Regenerative Medicine and Tissue Engineering, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Akihiko TaguchiDepartment of Regenerative Medicine Research, Institute of Biomedical Research and Innovation, Kobe, Hyogo, Japan.
Toshihiro SomaDivision of Hematology, Department of Internal Medicine, Hyogo Medical College, Nishinomiya, Hyogo, Japan.
Hiroyasu OgawaDivision of Hematology, Department of Internal Medicine, Hyogo Medical College, Nishinomiya, Hyogo, Japan.
Shinji KatsuragiDepartment of Perinatology, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Jun YoshimatsuDepartment of Perinatology, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Mariko Harada-ShibaDepartment of Regenerative Medicine and Tissue Engineering, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan ; Department of Molecular Innovation in Lipidology, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Kenji KangawaDepartment of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Tomoaki IkedaDepartment of Regenerative Medicine and Tissue Engineering, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan ; Department of Perinatology, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan ; Department of Obstetrics and Gynecology, Mie University School of Medicine, Tsu, Mie, Japan.
National Cerebral and Cardiovascular Center · JPHyogo Medical University · JPFoundation for Biomedical Research and Innovation · JPHokkaido University · JPMie University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although mesenchymal stem cells (MSCs) can be obtained from the fetal membrane (FM), little information is available regarding biological differences in MSCs derived from different layers of the FM or their therapeutic potential. Isolated MSCs from both amnion and chorion layers of FM showed similar morphological appearance, multipotency, and cell-surface antigen expression. Conditioned media obtained from amnion- and chorion-derived MSCs inhibited cell death caused by serum starvation or hypoxia in endothelial cells and cardiomyocytes. Amnion and chorion MSCs secreted significant amounts of angiogenic factors including HGF, IGF-1, VEGF, and bFGF, although differences in the cellular expression profile of these soluble factors were observed. Transplantation of human amnion or chorion MSCs significantly increased blood flow and capillary density in a murine hindlimb ischemia model. In addition, compared to human chorion MSCs, human amnion MSCs markedly reduced T-lymphocyte proliferation with the enhanced secretion of PGE2, and improved the pathological situation of a mouse model of acute graft-versus-host disease. Our results highlight that human amnion- and chorion-derived MSCs, which showed differences in their soluble factor secretion and angiogenic/immuno-suppressive function, could be ideal cell sources for regenerative medicine.

Indexed as

CytoprotectionImmunosuppression TherapyMesenchymal Stem Cell TransplantationNeovascularization, PhysiologicAmnionAnimalsChorionFemaleHindlimbHumansHuman Umbilical Vein Endothelial CellsIntercellular Signaling Peptides and ProteinsIschemiaMaleMesenchymal Stem CellsMiceIntercellular Signaling Peptides and Proteins

Identifiers

PMID24551087
PMCPMC3925106
OpenAlexW1980387222

What OpenQuestion holds

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LicenceCC BY
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.