Evidence map›Paper›PMID 27832825›Full record

ArticleStem cell research & therapy2016

Heterogeneity of proangiogenic features in mesenchymal stem cells derived from bone marrow, adipose tissue, umbilical cord, and placenta.

Wen Jing Du, Ying Chi, Zhou Xin Yang, Zong Jin Li, Jun Jie Cui, Bao Quan Song, Xue Li, Shao Guang Yang, Zhi Bo Han, Zhong Chao Han

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
12.1field-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.

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

106 citing papers in PubMed, 196 citations in OpenAlex.

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  20. Mesenchymal stem cells from different sources for sepsis treatment: prospects and limitations.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Review

46 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

Wen Jing DuThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China.
Ying ChiThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China.
Zhou Xin YangThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China.
Zong Jin LiBeijing Institute of Health and Stem Cells, No. 1, Kangding Road, BDA, Beijing, 100176, China.
Jun Jie CuiThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China.
Bao Quan SongThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China.
Xue LiThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China.
Shao Guang YangThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China.
Zhi Bo HanThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China. zhibohan@163.com.
Zhong Chao HanThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Hospital of Blood Disease, Chinese Academy of Medical Science & Peking Union Medical College, No. 288, Nanjing Road, Heping District, Tianjin, 300020, China. hanzhongchao@hotmail.com.
Institute of Hematology & Blood Diseases Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) have been widely proven effective for therapeutic angiogenesis in ischemia animal models as well as clinical vascular diseases. Because of the invasive method, limited resources, and aging problems of adult tissue-derived MSCs, more perinatal tissue-derived MSCs have been isolated and studied as promising substitutable MSCs for cell transplantation. However, fewer studies have comparatively studied the angiogenic efficacy of MSCs derived from different tissues sources. Here, we evaluated whether the in-situ environment would affect the angiogenic potential of MSCs.

methodsWe harvested MSCs from adult bone marrow (BMSCs), adipose tissue (AMSCs), perinatal umbilical cord (UMSCs), and placental chorionic villi (PMSCs), and studied their "MSC identity" by flow cytometry and in-vitro trilineage differentiation assay. Then we comparatively studied their endothelial differentiation capabilities and paracrine actions side by side in vitro.

resultsOur data showed that UMSCs and PMSCs fitted well with the minimum standard of MSCs as well as BMSCs and AMSCs. Interestingly, we found that MSCs regardless of their tissue origins could develop similar endothelial-relevant functions in vitro, including producing eNOS and uptaking ac-LDL during endothelial differentiation in spite of their feeble expression of endothelial-related genes and proteins. Additionally, we surprisingly found that BMSCs and PMSCs could directly form tubular structures in vitro on Matrigel and their conditioned medium showed significant proangiogenic bioactivities on endothelial cells in vitro compared with those of AMSCs and UMSCs. Besides, several angiogenic genes were upregulated in BMSCs and PMSCs in comparison with AMSCs and UMSCs. Moreover, enzyme-linked immunosorbent assay further confirmed that BMSCs secreted much more VEGF, and PMSCs secreted much more HGF and PGE2.

conclusionsOur study demonstrated the heterogeneous proangiogenic properties of MSCs derived from different tissue origins, and the in vivo isolated environment might contribute to these differences. Our study suggested that MSCs derived from bone marrow and placental chorionic villi might be preferred in clinical application for therapeutic angiogenesis.

Indexed as

Adipose TissueBone MarrowBone Marrow CellsCell DifferentiationCells, CulturedCulture Media, ConditionedEndothelial CellsFemaleHumansHuman Umbilical Vein Endothelial CellsMesenchymal Stem CellsNeovascularization, PhysiologicPlacentaPregnancyUmbilical CordCulture Media, ConditionedAdipose tissueBone marrowHeterogeneityMesenchymal stem cellsPlacental chorionic villiPro-angiogenic featuresUmbilical cord

Identifiers

PMID27832825
PMCPMC5103372
OpenAlexW2553749118

What OpenQuestion holds

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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.