Evidence map›Paper›PMID 11159214›Full record

ArticleThe American journal of pathology2001

Massive liver replacement by transplanted hepatocytes in the absence of exogenous growth stimuli in rats treated with retrorsine.

S Laconi, S Pillai, P P Porcu, D A Shafritz, P Pani, E Laconi

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 95 citations in OpenAlex.

  1. Cell competition in liver carcinogenesis.World journal of hepatology · 2020
    Review
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  12. Liver regeneration: alternative epithelial pathways.The international journal of biochemistry & cell biology · 2011
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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

6 authors at 4 institutions in 2 countries.

S LaconiDipartimento di Scienze Mediche e Biotecnologie, Sezione di Patologia Sperimentale, Università di Cagliari, Cagliari, Italy.
S Pillai
P P Porcu
D A Shafritz
P Pani
E Laconi
University of Cagliari · ITIstituto Nazionale di Fisica Nucleare, Sezione di Cagliari · ITOspedale Microcitemico · ITYeshiva University · US

Funding

Special Animal CoreP30DK041296 · NIDDK · YESHIVA UNIVERSITY · PI WOLKOFF, ALLAN W · 1989 to 2018
$22.9M
PROTEIN SYNTHESIS IN NORMAL AND REGENERATING LIVERR01DK017609 · NIDDK · YESHIVA UNIVERSITY · PI SHAFRITZ, DAVID A · 1986 to 2012
$5.1M
NIDDK NIH HHS P30 DK041296NIDDK NIH HHS P30 DK41296NIDDK NIH HHS R01 DK017609NIDDK NIH HHS R01 DK17609Telethon A.110
6 · The paper itself

Abstract

A strategy for hepatocyte transplantation was recently developed whereby massive replacement of the recipient liver is achieved after a combined treatment with retrorsine, a pyrrolizidine alkaloid, and partial hepatectomy. We now investigated whether liver repopulation could occur in this animal model in the absence of any exogenous growth stimuli (eg, partial hepatectomy) for the transplanted cells. Dipeptidyl-peptidase type IV-deficient (DPPIV-) rats were used as recipients. Rats were given two injections of retrorsine (30 mg/kg each, 2 weeks apart), followed by transplantation of 2 x 10(6) hepatocytes isolated from a normal, syngeneic, DPPIV+ donor. At 2 weeks after transplantation, clusters of DPPIV+ hepatocytes occupied 3.3 +/- 0.9% of host liver, increasing to 38.2 +/- 6.3% at 2 months, and to 65.9 +/- 8.8% at 5 months. By 1 year, >95% of the original hepatocytes were replaced by donor-derived cells. Serum parameters related both to hepatocyte function and integrity (including glucose, bilirubin, total proteins, cholinesterase, alanine aminotransferase, and alkaline phosphatase) were in the normal range in retrorsine-treated and repopulated animals. These results provide further insights toward developing strategies for effective liver repopulation by transplanted hepatocytes with reduced toxicity for the host and potential clinical applicability.

Indexed as

Cell TransplantationAnimalsBilirubinBlood GlucoseCell DivisionDipeptidyl Peptidase 4DNAFemaleGlutathione TransferaseHepatectomyHepatocytesIsoenzymesLiverLiver TransplantationMalePyrrolizidine AlkaloidsBilirubinBlood GlucoseDipeptidyl Peptidase 4DNAGlutathione TransferaseIsoenzymesPyrrolizidine Alkaloidsretrorsine

Identifiers

PMID11159214
PMCPMC1850302
OpenAlexW2118834966

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.