Evidence map›Paper›PMID 29705933›Full record

ArticleJournal of molecular neuroscience : MN2018

Mesenchymal Stem Cells Form 3D Clusters Following Intraventricular Transplantation.

Nicole Jungwirth, Laura Salinas Tejedor, Wen Jin, Viktoria Gudi, Thomas Skripuletz, Veronika Maria Stein, Andrea Tipold, Andrea Hoffmann, Martin Stangel, Wolfgang Baumgärtner and 1 more

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 16 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

11 authors at 2 institutions in 1 country.

Nicole JungwirthDepartment of Pathology, University of Veterinary Medicine Hannover, Bünteweg 17, 30559, Hanover, Germany.
Laura Salinas TejedorCenter for Systems Neuroscience, Hannover, Germany.
Wen JinDepartment of Pathology, University of Veterinary Medicine Hannover, Bünteweg 17, 30559, Hanover, Germany.
Viktoria GudiCenter for Systems Neuroscience, Hannover, Germany.
Thomas SkripuletzClinical Neuroimmunology and Neurochemistry, Department of Neurology, Hannover Medical School, Hannover, Germany.
Veronika Maria SteinDepartment of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Hannover, Germany.
Andrea TipoldCenter for Systems Neuroscience, Hannover, Germany.
Andrea HoffmannDepartment of Orthopaedic Surgery, Hannover Medical School, Hannover, Germany.
Martin StangelCenter for Systems Neuroscience, Hannover, Germany.
Wolfgang BaumgärtnerDepartment of Pathology, University of Veterinary Medicine Hannover, Bünteweg 17, 30559, Hanover, Germany. wolfgang.baumgaertner@tiho-hannover.de.
Florian HansmannDepartment of Pathology, University of Veterinary Medicine Hannover, Bünteweg 17, 30559, Hanover, Germany.ORCID http://orcid.org/0000-0001-6064-7728
University of Veterinary Medicine Hannover, Foundation · DEMedizinische Hochschule Hannover · DE

Funding

Deutsche Forschungsgemeinschaft BA 815/14-1,Deutsche Forschungsgemeinschaft STA 518/4-1Deutsche Forschungsgemeinschaft TI 309/4-2
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are regarded as an immune privileged cell type with numerous regeneration-promoting effects. The in vivo behavior of MSC and underlying mechanisms leading to their regenerative effects are largely unknown. The aims of this study were to comparatively investigate the in vivo behavior of canine (cMSC), human (hMSC), and murine MSC (mMSC) following intra-cerebroventricular transplantation. At 7 days post transplantation (dpt), clusters of cMSC, hMSC, and mMSC were detected within the ventricular system. At 49 dpt, cMSC-transplanted mice showed clusters mostly consisting of extracellular matrix lacking transplanted MSC. Similarly, hMSC-transplanted mice lacked MSC clusters at 49 dpt. Xenogeneic MSC transplantation was associated with a local T lymphocyte-dominated immune reaction at both time points. Interestingly, no associated inflammation was observed following syngeneic mMSC transplantation. In conclusion, transplanted MSC formed intraventricular cell clusters and exhibited a short life span in vivo. Xenogeneically in contrast to syngeneically transplanted MSC triggered a T cell-mediated graft rejection indicating that MSCs are not as immune privileged as previously assumed. However, MSC may mediate their effects by a "hit and run" mechanism and future studies will show whether syngeneically or xenogeneically transplanted MSCs exert better therapeutic effects in animals with CNS disease.

Indexed as

AnimalsCells, CulturedCerebral VentriclesDogsFemaleGraft RejectionHeterograftsHumansMaleMesenchymal Stem CellsMesenchymal Stem Cell TransplantationMiceMice, Inbred C57BLT-LymphocytesCanine mesenchymal stem cellsCD44Cell clustersHost versus graft reactionHuman mesenchymal stem cellsMesenchymal stem cells

Identifiers

PMID29705933
OpenAlexW2800993930

What OpenQuestion holds

Textmetadata
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.