Evidence map›Paper›PMID 27406089›Full record

ArticleMolecular imaging and biology2017

In Vivo Bioluminescence Imaging of Transplanted Mesenchymal Stromal Cells and Their Rejection Mediated by Intrahepatic NK Cells.

Jing-Jing Liu, Xiao-Jun Hu, Zheng-Ran Li, Rong-Hua Yan, Dan Li, Jin Wang, Hong Shan

Abstract read
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In one paragraph

Article in Molecular imaging and biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  3. CD4Aging and disease · 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

7 authors at 3 institutions in 1 country.

Jing-Jing LiuDepartment of Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.
Xiao-Jun HuGuangdong Provincial Engineering Research Center of Molecular Imaging, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, 519000, China.
Zheng-Ran LiDepartment of Radiology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China.
Rong-Hua YanDepartment of Radiology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China.
Dan LiGuangdong Provincial Engineering Research Center of Molecular Imaging, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, 519000, China.
Jin WangDepartment of Radiology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China.
Hong ShanGuangdong Provincial Engineering Research Center of Molecular Imaging, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, 519000, China. shanhong@mail.sysu.edu.cn.
Fifth Affiliated Hospital of Sun Yat-sen University · CNSun Yat-sen University · CNFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMesenchymal stromal cells (MSCs) hold promise in the treatment of liver disease. However, short survival time of MSCs after intrahepatic transplantation limits their value; therefore, understanding the basis of MSCs survival and rejection may increase their utility. This study was aimed at determining the role of intrahepatic natural killer (NK) cells on MSCs survival and their retention in the liver shortly after transplant. PROCEDURES: Human MSCs were labeled with the Luc2-mKate2 dual-fusion reporter gene (MSCs-R), and the residence time and survival of MSCs-R xenografts after intrahepatic transplantation were evaluated by in vivo bioluminescence imaging (BLI). Coculture of MSCs and NK cells was performed to assess cytotoxicity. To evaluate the role of NK cells in rejection of the xenografted cells, the fates of transplanted MSCs-R were then assessed in vivo by BLI after activation of intrahepatic NK cells.

resultsWe observed a linear correlation between luciferase activity from live MSCs-R and cell number in vitro (R

conclusionHuman MSCs could be followed dynamically in vivo by BLI, and the role of murine hepatic NK cells, especially activated NK cells, could be inferred from the loss of signals from MSCs. This finding may have practical clinical implications in MSCs transplantation in treating liver disease.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsCell DifferentiationCell LineCell ProliferationCoculture TechniquesFlow CytometryGenes, ReporterHumansInterleukin-15Killer Cells, NaturalLiverLuminescent MeasurementsLymphocyte ActivationMaleMesenchymal Stem CellsIl15ra protein, mouseInterleukin-15Receptors, Interleukin-15Bioluminescence imagingImmune rejectionLiver diseaseMesenchymal stem cellsXenograft

Identifiers

PMID27406089
OpenAlexW2470614240

What OpenQuestion holds

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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.