Evidence map›Paper›PMID 26039874›Full record

ArticleScientific reports2015

Extracellular Matrix can Recover the Downregulation of Adhesion Molecules after Cell Detachment and Enhance Endothelial Cell Engraftment.

Ningning He, Yang Xu, Wei Du, Xin Qi, Lu Liang, Yuebing Wang, Guowei Feng, Yan Fan, Zhongchao Han, Deling Kong and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 54 citations in OpenAlex.

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  11. Mesenchymal stem cells: A new therapeutic tool for chronic kidney disease.Frontiers in cell and developmental biology · 2022
    Review
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  19. Review
  20. Prostaglandin ETheranostics · 2018
    Article
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

14 authors at 4 institutions in 2 countries.

Ningning He1] Collaborative Innovation Center for Biotherapy, Nankai University School of Medicine, Tianjin, China [2] Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, Nankai University School of Medicine, Tianjin, China [3] The Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, China.
Yang Xu1] Collaborative Innovation Center for Biotherapy, Nankai University School of Medicine, Tianjin, China [2] Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, Nankai University School of Medicine, Tianjin, China.
Wei Du1] Collaborative Innovation Center for Biotherapy, Nankai University School of Medicine, Tianjin, China [2] Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, Nankai University School of Medicine, Tianjin, China [3] The Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, China.
Xin QiDepartment of Cardiology, Tianjin Union Medical Center, Nankai University Affiliated Hospital, Tianjin, China.
Lu Liang1] Collaborative Innovation Center for Biotherapy, Nankai University School of Medicine, Tianjin, China [2] State Key Lab of Experimental Hematology, Chinese Academy of Medical Sciences, Tianjin, China.
Yuebing Wang1] Collaborative Innovation Center for Biotherapy, Nankai University School of Medicine, Tianjin, China [2] Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, Nankai University School of Medicine, Tianjin, China.
Guowei Feng1] Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, Nankai University School of Medicine, Tianjin, China [2] The Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, China.
Yan Fan1] Collaborative Innovation Center for Biotherapy, Nankai University School of Medicine, Tianjin, China [2] Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, Nankai University School of Medicine, Tianjin, China.
Zhongchao HanState Key Lab of Experimental Hematology, Chinese Academy of Medical Sciences, Tianjin, China.
Deling KongThe Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, China.
Zhen ChengDepartment of Radiology and Molecular Imaging Program at Stanford (MIPS).
Joseph C WuStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Zuoxiang HeDepartment of Cardiac Nuclear Imaging, Fuwai Hospital, Peking Union Medical College &Chinese Academy of Medical Sciences, Beijing, China.
Zongjin Li1] Collaborative Innovation Center for Biotherapy, Nankai University School of Medicine, Tianjin, China [2] Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, Nankai University School of Medicine, Tianjin, China [3] The Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, China.
Nankai University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNCardiovascular Institute of the South · USStanford Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The low cell engraftment after transplantation limits the successful application of stem cell therapy and the exact pathway leading to acute donor cell death following transplantation is still unknown. Here we investigated if processes involved in cell preparation could initiate downregulation of adhesion-related survival signals, and further affect cell engraftment after transplantation. Human embryonic stem cell-derived endothelial cells (hESC-ECs) were suspended in PBS or Matrigel and kept at 4 °C. Quantitative RT-PCR analysis was used to test the adhesion and apoptosis genes' expression of hESC-ECs. We demonstrated that cell detachment can cause downregulation of cell adhesion and extracellular matrix (ECM) molecules, but no obvious cell anoikis, a form of apoptosis after cell detachment, was observed. The downregulation of adhesion and ECM molecules could be regained in the presence of Matrigel. Finally, we transplanted hESC-ECs into a mouse myocardial ischemia model. When transplanted with Matrigel, the long-term engraftment of hESC-ECs was increased through promoting angiogenesis and inhibiting apoptosis, and this was confirmed by bioluminescence imaging. In conclusion, ECM could rescue the functional genes expression after cell detached from culture dish, and this finding highlights the importance of increasing stem cell engraftment by mimicking stem cell niches through ECM application.

Indexed as

AnimalsApoptosisCell Adhesion MoleculesCell DifferentiationCell LineCell ProliferationCell SurvivalDisease Models, AnimalEmbryonic Stem CellsEndothelial CellsExtracellular MatrixFemaleGene ExpressionGene Expression ProfilingHumansMiceCell Adhesion Molecules

Identifiers

PMID26039874
PMCPMC4454140
OpenAlexW2252815101

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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.