Evidence map›Paper›PMID 27767181›Full record

ArticleScientific reports2016

Efficient recellularisation of decellularised whole-liver grafts using biliary tree and foetal hepatocytes.

Satoshi Ogiso, Kentaro Yasuchika, Ken Fukumitsu, Takamichi Ishii, Hidenobu Kojima, Yuya Miyauchi, Ryoya Yamaoka, Junji Komori, Hokahiro Katayama, Takayuki Kawai and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  5. [Liver organoid technology and its related progress in liver disease research].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    Review
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  8. Review
  9. Article
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  11. Article
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  13. Article
  14. Recent Advances in Liver Engineering With Decellularized Scaffold.Frontiers in bioengineering and biotechnology · 2022
    Review
  15. Review
  16. 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

14 authors at 1 institution in 1 country.

Satoshi OgisoDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Kentaro YasuchikaDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Ken FukumitsuDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takamichi IshiiDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hidenobu KojimaDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Yuya MiyauchiDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Ryoya YamaokaDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Junji KomoriDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hokahiro KatayamaDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takayuki KawaiDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Elena Yukie YoshitoshiDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Sadahiko KitaDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Katsutaro YasudaDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Shinji UemotoDepartment of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Kyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A whole-organ regeneration approach, using a decellularised xenogeneic liver as a scaffold for the construction of a transplantable liver was recently reported. Deriving suitable scaffolds was the first step towards clinical application; however, effective recellularisation remains to be achieved. This report presents a strategy for the improvement of the recellularisation process, using novel cell-seeding technique and cell source. We evaluated recellularised liver grafts repopulated through the portal vein or the biliary duct with mice adult hepatocytes or E14.5 foetal hepatocytes. More than 80% of the cells seeded through the biliary tree entered the parenchyma beyond the ductule-lining matrix barrier and distributed throughout the liver lobule. In contrast, about 20% of the cells seeded through the portal tree entered the parenchyma. The gene expression levels of foetal hepatocyte albumin, glucose 6-phosphatase, transferrin, cytokeratin 19, and gamma-glutamyl transpeptidase were increased in three-dimensional cultures in the native liver-derived scaffolds, and the activation of liver detoxification enzymes and formation of biliary duct-like structures were supported. The metabolic functions of liver grafts recellularised with different cell types were similar. These results suggest that biliary tree cell-seeding approach is promising, and that liver progenitor cells represent a good cell source candidate.

Indexed as

AnimalsBile DuctsCell Culture TechniquesCells, CulturedFetusgamma-GlutamyltransferaseGlucose-6-PhosphataseHepatocytesKeratin-19LiverLiver RegenerationMaleMiceMice, Inbred C57BLMicroscopy, FluorescenceParenchymal Tissuegamma-GlutamyltransferaseGlucose-6-PhosphataseKeratin-19Transferrins

Identifiers

PMID27767181
PMCPMC5073336
OpenAlexW2536272890

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LicenceCC BY
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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.