Evidence map›Paper›PMID 23625886›Full record

ArticleJournal of biomedical materials research. Part A2014

Decellularized liver scaffolds effectively support the proliferation and differentiation of mouse fetal hepatic progenitors.

Xiaojun Wang, Jing Cui, Bing-Qiang Zhang, Hongyu Zhang, Yang Bi, Quan Kang, Ning Wang, Ping Bie, Zhanyu Yang, Huaizhi Wang and 6 more

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

  1. Article
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  5. Immortalization Reversibility in the Context of Cell Therapy Biosafety.International journal of molecular sciences · 2023
    Review
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  13. Article
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  16. Hepatocytic differentiation of iPS cells on decellularized liver tissue.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. 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

16 authors.

Xiaojun WangInstitute of Hepatobiliary Surgery, Southwest Hospital, Third Military Medical University, Chongqing, 400038, China; Department of Surgery, Molecular Oncology Laboratory, The University of Chicago Medical Center, Chicago, Illinois, 60637.
Jing Cui
Bing-Qiang Zhang
Hongyu Zhang
Yang Bi
Quan Kang
Ning Wang
Ping Bie
Zhanyu Yang
Huaizhi Wang
Xiangde Liu
Rex C Haydon
Hue H Luu
Ni Tang
Jiahong Dong
Tong-Chuan He

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Regulation of beta-Catenin Signaling by Tyrosine PhosphorylationR01CA106569 · NCI · UNIVERSITY OF CHICAGO · PI HE, TONG-CHUAN · 2006 to 2010
$1.3M
NCATS NIH HHS UL1 TR000430NCI NIH HHS R01 CA106569
6 · The paper itself

Abstract

Decellularized whole organs represent ideal scaffolds for engineering new organs and/or cell transplantation. Here, we investigate whether decellularized liver scaffolds provide cell-friendly biocompatible three-dimensional (3-D) environment to support the proliferation and differentiation of hepatic progenitor cells. Mouse liver tissues are efficiently decellularized through portal vein perfusion. Using the reversibly immortalized mouse fetal hepatic progenitor cells (iHPCs), we are able to effectively recellularize the decellularized liver scaffolds. The perfused iHPCs survive and proliferate in the 3-D scaffolds in vitro for 2 weeks. When the recellularized scaffolds are implanted into the kidney capsule of athymic nude mice, cell survival and proliferation of the implanted scaffolds are readily detected by whole body imaging for 10 days. Furthermore, epidermal growth factor (EGF) is shown to significantly promote the proliferation and differentiation of the implanted iHPCs. Histologic and immunochemical analyzes indicate that iHPCs are able to proliferate and differentiate to mature hepatocytes upon EGF stimulation in the scaffolds. The recellularization of the biomaterial scaffolds is accompanied with vascularization. Taken together, these results indicate that decullarized liver scaffolds effectively support the proliferation and differentiation of iHPCs, suggesting that decellularized liver matrix may be used as ideal biocompatible scaffolds for hepatocyte transplantation.

Indexed as

Cell DifferentiationAnimalsCell Line, TransformedCell ProliferationCell SurvivalEpidermal Growth FactorFetusHEK293 CellsHepatocytesHumansLiverMaleMiceMice, Inbred BALB CMice, NudePerfusionEpidermal Growth Factorcell transplantationdecellularized scaffoldsimmortalized progenitorsliver progenitor cellsregenerative medicinetissue engineering

Identifiers

PMID23625886
PMCPMC4056447

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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.