Evidence map›Paper›PMID 27586516›Full record

ArticleScientific reports2016

Role of IGF1R(+) MSCs in modulating neuroplasticity via CXCR4 cross-interaction.

Hsu-Tung Lee, Hao-Teng Chang, Sophie Lee, Chen-Huan Lin, Jia-Rong Fan, Shinn-Zong Lin, Chung Y Hsu, Chia-Hung Hsieh, Woei-Cherng Shyu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Hsu-Tung LeeDepartment of Neurosurgery, Taichung Veterans General Hospital, Taichung, 40421, Taiwan.
Hao-Teng ChangGraduate Institute of Basic Medical Science, China Medical University, Taichung, 40421, Taiwan.
Sophie LeeCenter for Neuropsychiatry, China Medical University Hospital, Taichung, 40440, Taiwan.
Chen-Huan LinCenter for Neuropsychiatry, China Medical University Hospital, Taichung, 40440, Taiwan.
Jia-Rong FanCenter for Neuropsychiatry, China Medical University Hospital, Taichung, 40440, Taiwan.
Shinn-Zong LinCenter for Neuropsychiatry, China Medical University Hospital, Taichung, 40440, Taiwan.
Chung Y HsuGraduate Institute of Clinical Medical Science, China Medical University, Taichung, 40421, Taiwan.
Chia-Hung HsiehGraduate Institute of Basic Medical Science, China Medical University, Taichung, 40421, Taiwan.
Woei-Cherng ShyuCenter for Neuropsychiatry, China Medical University Hospital, Taichung, 40440, Taiwan.
China Medical University · TWChina Medical University Hospital · TWNational Defense Medical Center · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To guide the use of human mesenchymal stem cells (MSCs) toward clinical applications, identifying pluripotent-like-markers for selecting MSCs that retain potent self-renewal-ability should be addressed. Here, an insulin-like growth factor 1 receptor (IGF1R)-expressing sub-population in human dental pulp MSCs (hDSCs), displayed multipotent properties. IGF1R expression could be maintained in hDSCs when they were cultured in 2% human cord blood serum (hUCS) in contrast to that in 10% fetal calf serum (FCS). Cytokine array showed that hUCS contained higher amount of several growth factors compared to FCS, including IGF-1 and platelet-derived growth factor (PDGF-BB). These cytokines modulates the signaling events in the hDSCs and potentially enhances engraftment upon transplantation. Specifically, a bidirectional cross-talk between IGF1R/IGF1 and CXCR4/SDF-1α signaling pathways in hDSCs, as revealed by interaction of the two receptors and synergistic activation of both signaling pathways. In rat stroke model, animals receiving IGF1R(+) hDSCs transplantation, interaction between IGF1R and CXCR4 was demonstrated to promote neuroplasticity, therefore improving neurological function through increasing glucose metabolic activity, enhancing angiogenesis and anti-inflammatiory effects. Therefore, PDGF in hUCS-culture system contributed to the maintenance of the expression of IGF1R in hDSCs. Furthermore, implantation of IGF1R(+) hDSCs exerted enhanced neuroplasticity via integrating inputs from both CXCR4 and IGF1R signaling pathways.

Indexed as

Neuronal PlasticityAnimalsAnti-Inflammatory AgentsApoptosisBecaplerminBrain IschemiaCerebrovascular CirculationChemokine CXCL12ChildChild, PreschoolCytokinesDental PulpGlucoseHumansInsulin-Like Growth Factor IMaleAnti-Inflammatory AgentsBecaplerminChemokine CXCL12CXCR4 protein, humanCytokinesGlucoseInsulin-Like Growth Factor IProto-Oncogene Proteins c-sisReceptor, IGF Type 1Receptors, CXCR4

Identifiers

PMID27586516
PMCPMC5009335
OpenAlexW2507365676

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.