Evidence map›Paper›PMID 28009756›Full record

ArticleTransplantation2017

Regeneration and Cell Recruitment in an Improved Heterotopic Auxiliary Partial Liver Transplantation Model in the Rat.

Yoshihiro Ono, Angelica Pérez-Gutiérrez, Mladen I Yovchev, Kentaro Matsubara, Shinichiro Yokota, Jorge Guzman-Lepe, Kan Handa, Alexandra Collin de l'Hortet, Angus W Thomson, David A Geller and 3 more

Open access · hybridAbstract readVideo-Audio Media
In one paragraph

Article in Transplantation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  4. Review
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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

13 authors at 1 institution in 5 countries.

Yoshihiro Ono1 Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA.2 Department of Surgery, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo, Japan.3 Thomas E Starzl Transplantation Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA.4 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA.
Angelica Pérez-Gutiérrez
Mladen I Yovchev
Kentaro Matsubara
Shinichiro Yokota
Jorge Guzman-Lepe
Kan Handa
Alexandra Collin de l'Hortet
Angus W Thomson
David A Geller
Hiroshi Yagi
Michael Oertel
Alejandro Soto-Gutierrez
Apple (Israel) · IL

Funding

Mini-Livers Derived from Human IPS Cells for Modeling Steatosis and TherapyR01DK099257 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NAGRATH, DEEPAK, SOTO-GUTIERREZ, ALEJANDRO · 2014 to 2024
$3.4M
The role of activin A in mediating liver repopulation after cell transplantationR01DK090325 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI OERTEL, MICHAEL · 2011 to 2015
$1.5M
Engineering of hepatic grafts with decellularized native matricesR00DK083556 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SOTO-GUTIERREZ, ALEJANDRO · 2011 to 2013
$707k
NIDDK NIH HHS R00 DK083556NIDDK NIH HHS R01 DK090325NIDDK NIH HHS R01 DK099257
6 · The paper itself

Abstract

backgroundAuxiliary partial liver transplantation (APLT) in humans is a therapeutic modality used especially to treat liver failure in children or congenital metabolic disease. Animal models of APLT have helped to explore therapeutic options. Though many groups have suggested improvements, standardizing the surgical procedure has been challenging. Additionally, the question of whether graft livers are reconstituted by recipient-derived cells after transplantation has been controversial. The aim of this study was to improve experimental APLT in rats and to assess cell recruitment in the liver grafts.

methodsTo inhibit recipient liver regeneration and to promote graft regeneration, we treated recipients with retrorsine and added arterial anastomosis. Using green fluorescence protein transgenic rats as recipients, we examined liver resident cell recruitment within graft livers by immunofluorescence costaining.

resultsIn the improved APLT model, we achieved well-regenerated grafts that could maintain regeneration for at least 4 weeks. Regarding the cell recruitment, there was no evidence of recipient-derived hepatocyte, cholangiocyte, or hepatic stellate cell recruitment into the graft. Macrophages/monocytes, however, were consistently recruited into the graft and increased over time, which might be related to inflammatory responses. Very few endothelial cells showed colocalization of markers.

conclusionsWe have successfully established an improved rat APLT model with arterial anastomosis as a standard technique. Using this model, we have characterized cell recruitment into the regenerating grafts.

Indexed as

Cell MovementCell ProliferationLiver RegenerationAnimalsCell LineageGreen Fluorescent ProteinsLiverLiver TransplantationMaleModels, AnimalPyrrolizidine AlkaloidsRats, Inbred F344Rats, Sprague-DawleyRats, TransgenicTime Factorsenhanced green fluorescent proteinGreen Fluorescent ProteinsPyrrolizidine Alkaloidsretrorsine

Identifiers

PMID28009756
PMCPMC5193171
OpenAlexW2529649456

What OpenQuestion holds

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LicenceTDM
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.