Evidence map›Paper›PMID 18292182›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2008

Activation of innate immunity (NK/IFN-gamma) in rat allogeneic liver transplantation: contribution to liver injury and suppression of hepatocyte proliferation.

Kezhen Shen, Shu-Sen Zheng, Ogyi Park, Hua Wang, Zhaoli Sun, Bin Gao

Open access · greenAbstract readComparative Study
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. The Role of Interferon Regulatory Factors in Liver Diseases.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Mitofusin-2 mediated mitochondrial CaWorld journal of gastroenterology · 2017
    Article
  10. Review
  11. Genomic regulation of senescence and innate immunity signaling in the retinal pigment epithelium.Mammalian genome : official journal of the International Mammalian Genome Society · 2015
    Article
  12. Article
  13. Article
  14. Article
  15. Regulation of hepatocyte fate by interferon-γ.Cytokine & growth factor reviews · 2011
    Review
  16. Toll-like receptor 3 in liver diseases.Gastroenterology research and practice · 2010
    Article
  17. 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

6 authors at 2 institutions in 2 countries.

Kezhen ShenDepartment of Hepatobiliary Surgery, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Shu-Sen Zheng
Ogyi Park
Hua Wang
Zhaoli Sun
Bin Gao
National Institutes of Health · USZhejiang University · CN

Funding

Immunity, liver injury and repairZ01AA000368 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GAO, BIN · 2002 to 2008
$1.2M
Intramural NIH HHS Z01 AA000368
6 · The paper itself

Abstract

Liver transplantation is presently the only curative treatment for patients with end-stage liver disease. However, the mechanisms underlying liver injury and hepatocyte proliferation posttransplantation remain obscure. In this investigation, liver injury and hepatocyte proliferation in syngeneic and allogeneic animal models were compared. Male Lewis and Dark Agouti (DA) rats were subjected to orthotopic liver transplantation (OLT). Rat OLT was performed in syngeneic (Lewis-Lewis) and allogeneic (Lewis-DA or DA-Lewis) animal models. Allogeneic liver grafts exhibited greater injury and cellular apoptosis than syngeneic grafts but less hepatocyte proliferation after OLT. Expression of IFN-gamma mRNA and activation of the downstream signal transducer and activator of transcription 1 (STAT1) and genes (interferon regulatory factor-1 and cyclin-dependent kinase inhibitor p21(CDKN1A)) were also greater in the allogeneic grafts compared with the syngeneic grafts. In contrast, STAT3 activation was lower in the allogeneic grafts. Furthermore, in the allogeneic grafts, depletion of natural killer (NK) cells decreased IFN-gamma/STAT1 activation but enhanced hepatocyte proliferation. These findings suggest that, compared with syngeneic transplantation, innate immunity (NK/IFN-gamma) is activated after allogeneic transplantation, which likely contributes to liver injury and inhibits hepatocyte proliferation.

Indexed as

Cell ProliferationImmunity, InnateLiver TransplantationAnimalsApoptosisCyclin-Dependent Kinase Inhibitor p21Graft RejectionHepatocytesImmune ToleranceInterferon-gammaInterferon Regulatory Factor-1Killer Cells, NaturalLiverLiver RegenerationMaleRatsCdkn1a protein, ratCyclin-Dependent Kinase Inhibitor p21Interferon-gammaInterferon Regulatory Factor-1Irf1 protein, ratRNA, MessengerStat1 protein, ratSTAT1 Transcription FactorStat3 protein, ratSTAT3 Transcription Factor

Identifiers

PMID18292182
PMCPMC2405895
OpenAlexW2114994536

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.