Evidence map›Paper›PMID 24488046›Full record

ArticleOrganogenesis

Mesenchymal stem cells support hepatocyte function in engineered liver grafts.

Yoshie Kadota, Hiroshi Yagi, Kenta Inomata, Kentaro Matsubara, Taizo Hibi, Yuta Abe, Minoru Kitago, Masahiro Shinoda, Hideaki Obara, Osamu Itano and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Organogenesis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
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  11. In Vivo Performance of Decellularized Vascular Grafts: A Review Article.International journal of molecular sciences · 2018
    Review
  12. Review
  13. Whole Organ Tissue Vascularization: Engineering the Tree to Develop the Fruits.Frontiers in bioengineering and biotechnology · 2018
    Review
  14. Article
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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.

Yoshie KadotaDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Hiroshi YagiDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Kenta InomataDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Kentaro MatsubaraDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Taizo HibiDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Yuta AbeDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Minoru KitagoDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Masahiro ShinodaDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Hideaki ObaraDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Osamu ItanoDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Yuko KitagawaDepartment of Surgery; Keio University; School of Medicine; Tokyo, Japan.
Keio University · JPIndiana University School of Medicine

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies suggest that organ decellularization is a promising approach to facilitate the clinical application of regenerative therapy by providing a platform for organ engineering. This unique strategy uses native matrices to act as a reservoir for the functional cells which may show therapeutic potential when implanted into the body. Appropriate cell sources for artificial livers have been debated for some time. The desired cell type in artificial livers is primary hepatocytes, but in addition, other supportive cells may facilitate this stem cell technology. In this context, the use of mesenchymal stem cells (MSC) is an option meeting the criteria for therapeutic organ engineering. Ideally, supportive cells are required to (1) reduce the hepatic cell mass needed in an engineered liver by enhancing hepatocyte function, (2) modulate hepatic regeneration in a paracrine fashion or by direct contact, and (3) enhance the preservability of parenchymal cells during storage. Here, we describe enhanced hepatic function achieved using a strategy of sequential infusion of cells and illustrate the advantages of co-cultivating bone marrow-derived MSCs with primary hepatocytes in the engineered whole-liver scaffold. These co-recellularized liver scaffolds colonized by MSCs and hepatocytes were transplanted into live animals. After blood flow was established, we show that expression of adhesion molecules and proangiogenic factors was upregulated in the graft.

Indexed as

Liver TransplantationAngiogenesis Inducing AgentsAnimalsCell Adhesion MoleculesCell CountFemaleHepatocytesLiverMesenchymal Stem CellsRats, Inbred LewTissue EngineeringTissue ScaffoldsAngiogenesis Inducing AgentsCell Adhesion Moleculescell transplantationorgan transplantationregenerative medicinescaffold matrixstem celltissue engineering

Identifiers

PMID24488046
PMCPMC4154962
OpenAlexW2142076588

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.