Evidence map›Paper›PMID 28785147›Full record

ArticleWorld journal of gastroenterology2017

Human liver chimeric mouse model based on diphtheria toxin-induced liver injury.

Xiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Mice Engrafted with Human Liver Cells.Seminars in liver disease · 2024
    Review
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

10 authors at 2 institutions in 1 country.

Xiao-Nan RenXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Rong-Rong RenXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Hua YangXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Bo-Yin QinXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Xiu-Hua PengXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Li-Xiang ChenXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Shun LiXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Meng-Jiao YuanXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Chao WangXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Xiao-Hui ZhouXiao-Nan Ren, Rong-Rong Ren, Hua Yang, Bo-Yin Qin, Xiu-Hua Peng, Li-Xiang Chen, Shun Li, Meng-Jiao Yuan, Chao Wang, Xiao-Hui Zhou, Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China.
Shanghai Public Health Clinical Center · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo establish an inducible liver injury mouse model and transplant human hepatocytes to obtain liver-humanized mice.

methodsWe crossed three mouse strains, including albumin (Alb)-cre transgenic mice, inducible diphtheria toxin receptor (DTR) transgenic mice and severe combined immune deficient (SCID)-beige mice, to create Alb-cre/DTR/SCID-beige (ADSB) mice, which coincidentally harbor Alb-cre and DTR transgenes and are immunodeficient. As the Cre expression is driven by the liver-specific promoter Alb (encoding ALB), the DTR stop signal flanked by two loxP sites can be deleted in the ADSB mice, resulting in DTR expression in the liver. ADSB mice aged 8-10 wk were injected intraperitoneally (i.p.) with diphtheria toxin (DT) and liver damage was assessed by serum alanine aminotransferase (ALT) level. Two days later, mouse livers were sampled for histological analysis, and human hepatocytes were transplanted into the livers on the same day. A human ALB enzyme-linked immunosorbent assay was performed 7, 14, 21 and 28 d after transplantation. Human CD68 immunohistochemistry was performed 30 and 90 d after transplantation.

resultsWe crossed Alb-cre with DTR and SCID-beige mice to obtain ADSB mice. These mice were found to have liver damage 4 d after i.p. injection of 2.5 ng/g bodyweight DT. Bodyweight began to decrease on day 2, increased on day 7, and was lowest on day 4 (range, 10.5%-13.4%). Serum ALT activity began to increase on day 2 and reached a peak value of 289.7 ± 16.2 IU/mL on day 4, then returned to background values on day 7. After transplantation of human liver cells, peripheral blood human ALB level was 1580 ± 454.8 ng/mL (range, 750.2-3064.9 ng/mL) after 28 d and Kupffer cells were present in the liver at 30 d in ADSB mice.

conclusionHuman hepatocytes were successfully repopulated in the livers of ADSB mice. The inducible mouse model of humanized liver in ADSB mice may have functional applications, such as hepatocyte transplantation, hepatic regeneration and drug metabolism.

Indexed as

Disease Models, AnimalAlanine TransaminaseAnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 MoleculeCell ProliferationDiphtheria ToxinEnzyme-Linked Immunosorbent AssayHeparin-binding EGF-like Growth FactorHepatocytesHumansImmunohistochemistryIntegrasesLiverLiver Failure, AcuteAlanine TransaminaseAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 antigen, humanCD68 MoleculeCre recombinaseDiphtheria ToxinHeparin-binding EGF-like Growth FactorIntegrasesDiphtheria toxinLiver chimeric mouse modelLiver diseaseLiver injury

Identifiers

PMID28785147
PMCPMC5526763
OpenAlexW2736951538

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.