Evidence map›Paper›PMID 25071759›Full record

ArticleFrontiers in immunology2014

Embryonic Stem Cells Promoting Macrophage Survival and Function are Crucial for Teratoma Development.

Tianxiang Chen, Xi Wang, Lei Guo, Mingmei Wu, Zhaoxia Duan, Jing Lv, Wenjiao Tai, Hemamalini Renganathan, Ruth Didier, Jinhua Li and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  7. Emerging roles of IL-34 in health and disease.The Journal of experimental medicine · 2020
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  14. Immunoregulatory properties of the cytokine IL-34.Cellular and molecular life sciences : CMLS · 2017
    Review
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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

16 authors at 8 institutions in 3 countries.

Tianxiang ChenW. M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey , New Jersey, NJ , USA ; Department of Thoracic Surgery, First Affiliated Hospital, School of Medicine, Zhejiang University , Hangzhou , China.
Xi WangW. M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey , New Jersey, NJ , USA ; Institute of Neurosciences, The Fourth Military Medical University , Xian , China.
Lei GuoDepartment of Biomedical Sciences, Florida State University College of Medicine , Tallahassee, FL , USA ; Department of Orthopedic Surgery, The Second Hospital of Xian Jiaotong University , Xian , China.
Mingmei WuW. M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey , New Jersey, NJ , USA.
Zhaoxia DuanW. M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey , New Jersey, NJ , USA.
Jing LvDepartment of Biomedical Sciences, Florida State University College of Medicine , Tallahassee, FL , USA.
Wenjiao TaiDepartment of Biomedical Sciences, Florida State University College of Medicine , Tallahassee, FL , USA.
Hemamalini RenganathanW. M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey , New Jersey, NJ , USA.
Ruth DidierDepartment of Biomedical Sciences, Florida State University College of Medicine , Tallahassee, FL , USA.
Jinhua LiDepartment of Anatomy and Developmental Biology, Monash University , Clayton, VIC , Australia.
Dongming SunW. M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey , New Jersey, NJ , USA.
Xiaoming ChenInstitute of Translational Medicine, First Affiliated Hospital, Wenzhou Medical University , Wenzhou , China.
Xijing HeDepartment of Orthopedic Surgery, The Second Hospital of Xian Jiaotong University , Xian , China.
Jianqing FanStatistics Laboratory, Princeton University , Princeton, NJ , USA.
Wise YoungW. M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey , New Jersey, NJ , USA.
Yi RenDepartment of Biomedical Sciences, Florida State University College of Medicine , Tallahassee, FL , USA.
Florida State University · USRutgers, The State University of New Jersey · USAir Force Medical University · CNFirst Affiliated Hospital of Wenzhou Medical University · CNMonash University · AUPrinceton University · USSecond Affiliated Hospital of Xi'an Jiaotong University · CNZhejiang University · CN

Funding

Quantitative Methods for Genome-wide Analysis of Macrophage Activation by ESCsR01GM100474 · NIGMS · PRINCETON UNIVERSITY · PI FAN, JIANQING · 2011 to 2014
$1.5M
NIGMS NIH HHS R01 GM100474
6 · The paper itself

Abstract

Stem cell therapies have had tremendous potential application for many diseases in recent years. However, the tumorigenic properties of stem cells restrict their potential clinical application; therefore, strategies for reducing the tumorigenic potential of stem cells must be established prior to transplantation. We have demonstrated that syngeneic transplantation of embryonic stem cells (ESCs) provokes an inflammatory response that involves the rapid recruitment of bone marrow-derived macrophages (BMDMs). ESCs are able to prevent mature macrophages from macrophage colony-stimulating factor (M-CSF) withdrawal-induced apoptosis, and thus prolong macrophage lifespan significantly by blocking various apoptotic pathways in an M-CSF-independent manner. ESCs express and secrete IL-34, which may be responsible for ESC-promoted macrophage survival. This anti-apoptotic effect of ESCs involves activation of extracellular signal-regulated kinase (ERK)1/2 and PI3K/Akt pathways and thus, inhibition of ERK1/2 and PI3K/AKT activation decreases ESC-induced macrophage survival. Functionally, ESC-treated macrophages also showed a higher level of phagocytic activity. ESCs further serve to polarize BMDMs into M2-like macrophages that exhibit most tumor-associated macrophage phenotypic and functional features. ESC-educated macrophages produce high levels of arginase-1, Tie-2, and TNF-α, which participate in angiogenesis and contribute to teratoma progression. Our study suggests that induction of M2-like macrophage activation is an important mechanism for teratoma development. Strategies targeting macrophages to inhibit teratoma development would increase the safety of ESC-based therapies, inasmuch as the depletion of macrophages completely inhibits ESC-induced angiogenesis and teratoma development.

Indexed as

angiogenesisapoptosisembryonic stem cellsmacrophagesteratoma

Identifiers

PMID25071759
PMCPMC4082241
OpenAlexW2119480335

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.