Evidence map›Paper›PMID 27977747›Full record

ArticlePloS one2016

Impact of NKT Cells and LFA-1 on Liver Regeneration under Subseptic Conditions.

Ann-Kathrin Jörger, Lei Liu, Karin Fehlner, Tanja Weisser, Zhangjun Cheng, Miao Lu, Bastian Höchst, Andreas Bolzer, Baocai Wang, Daniel Hartmann and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
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

16 authors at 3 institutions in 1 country.

Ann-Kathrin JörgerDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Lei LiuDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Karin FehlnerDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Tanja WeisserDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Zhangjun ChengDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Miao LuDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Bastian HöchstInstitute of Molecular Immunology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Andreas BolzerCarl Zeiss Microscopy, ZEISS group, Munich, Germany.
Baocai WangDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Daniel HartmannDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Volker AssfalgDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Yoshiaki SunamiDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Anna Melissa SchlitterInstitute of Pathology, Technische Universität München, Munich, Germany.
Helmut FriessDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Norbert HüserDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Melanie LaschingerDepartment of Surgery, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Klinikum rechts der Isar · DETechnical University of Munich · DECarl Zeiss (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundActivation of the immune system in terms of subseptic conditions during liver regeneration is of paramount clinical importance. However, little is known about molecular mechanisms and their mediators that control hepatocyte proliferation. We sought to determine the functional role of immune cells, especially NKT cells, in response to partial hepatectomy (PH), and to uncover the impact of the integrin lymphocyte function-associated antigen-1 (LFA-1) on liver regeneration in a subseptic setting.

methodsWild-type (WT) and LFA-1-/- mice underwent a 2/3 PH and low-dose lipopolysaccharid (LPS) application. Hepatocyte proliferation, immune cell infiltration, and cytokine profile in the liver parenchyma were determined.

resultsLow-dose LPS application after PH results in a significant delay of liver regeneration between 48h and 72h, which is associated with a reduced number of CD3+ cells within the regenerating liver. In absence of LFA-1, an impaired regenerative capacity was observed under low-dose LPS application. Analysis of different leukocyte subpopulations showed less CD3+NK1.1+ NKT cells in the liver parenchyma of LFA-1-/- mice after PH and LPS application compared to WT controls, while CD3-NK1.1+ NK cells markedly increased. Concordantly with this observation, lower levels of NKT cell related cytokines IL-12 and IL-23 were expressed in the regenerating liver of LFA-1-/- mice, while the expression of NK cell-associated CCL5 and IL-10 was increased compared to WT mice.

conclusionA subseptic situation negatively alters hepatocyte proliferation. Within this scenario, we suggest an important impact of NKT cells and postulate a critical function for LFA-1 during processes of liver regeneration.

Indexed as

AnimalsCells, CulturedInflammationInterleukin-6LipopolysaccharidesLiverLiver RegenerationLymphocyte Function-Associated Antigen-1MiceMice, Inbred C57BLNatural Killer T-CellsParenchymal TissuePhosphorylationSTAT3 Transcription FactorSuppressor of Cytokine Signaling 3 ProteinInterleukin-6LipopolysaccharidesLymphocyte Function-Associated Antigen-1Socs3 protein, mouseSTAT3 Transcription FactorSuppressor of Cytokine Signaling 3 Protein

Identifiers

PMID27977747
PMCPMC5158001
OpenAlexW2562635227

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.