Evidence map›Paper›PMID 23159949›Full record

ArticleThe American journal of pathology2013

Gut bacteria drive Kupffer cell expansion via MAMP-mediated ICAM-1 induction on sinusoidal endothelium and influence preservation-reperfusion injury after orthotopic liver transplantation.

Natasha Corbitt, Shoko Kimura, Kumiko Isse, Susan Specht, Lisa Chedwick, Brian R Rosborough, John G Lunz, Noriko Murase, Shinichiro Yokota, Anthony J Demetris

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 84 citations in OpenAlex.

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  14. Gut microbiota and immunity relevance in eubiosis and dysbiosis.Saudi journal of biological sciences · 2022
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  18. The Immune System through the Lens of Alcohol Intake and Gut Microbiota.International journal of molecular sciences · 2021
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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

10 authors at 1 institution in 1 country.

Natasha CorbittDivision of Transplantation, Department of Pathology, University of Pittsburgh Medical Center, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA.
Shoko Kimura
Kumiko Isse
Susan Specht
Lisa Chedwick
Brian R Rosborough
John G Lunz
Noriko Murase
Shinichiro Yokota
Anthony J Demetris
University of Pittsburgh Medical Center · US

Funding

PILOT AND FEASIBILITY STUDIESP30DK034987 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ROBERT S. SANDLER · 1985 to 2026
$30.5M
Interdisciplinary Training in Transplantation BiologyT32AI074490 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Angus W Thomson · 2007 to 2026
$4.2M
The Role of Gut Bacteria in Kupffer Cell Development and FunctionF31DK089902 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CORBITT, NATASHA · 2010 to 2013
$124k
NIAID NIH HHS T32 AI074490NIDDK NIH HHS F31 DK089902NIDDK NIH HHS F31DK089902-01NIDDK NIH HHS P30 DK034987NIDDK NIH HHS P30 DK34987PHS HHS P01 A1081678
6 · The paper itself

Abstract

Bacteria in the gut microbiome shed microbial-associated molecule patterns (MAMPs) into the portal venous circulation, where they augment various aspects of systemic immunity via low-level stimulation. Because the liver is immediately downstream of the intestines, we proposed that gut-derived MAMPs shape liver immunity and affect Kupffer cell (KC) phenotype. Germ-free (GF), antibiotic-treated (AVMN), and conventional (CL) mice were used to study KC development, function, and response to the significant stress of cold storage, reperfusion, and orthotopic transplantation. We found that a cocktail of physiologically active MAMPs translocate into the portal circulation, with flagellin (Toll-like receptor 5 ligand) being the most plentiful and capable of promoting hepatic monocyte influx in GF mice. In MAMP-deficient GF or AVMN livers, KCs are lower in numbers, have higher phagocytic activity, and have lower major histocompatibility complex II expression. MAMP-containing CL livers harbor significantly increased KC numbers via induction of intercellular adhesion molecule 1 on liver sinusoidal endothelium. These CL KCs have a primed yet expected phenotype, with increased major histocompatibility complex class II and lower phagocytic activity that increases susceptibility to liver preservation/reperfusion injury after orthotopic transplantation. The KC number, functional activity, and maturational status are directly related to the concentration of gut-derived MAMPs and can be significantly reduced by broad-spectrum antibiotics, thereby affecting susceptibility to injury.

Indexed as

AnimalsBacteriaBacterial TranslocationCecumEndothelium, VascularGerm-Free LifeGlycoproteinsImmunophenotypingIntercellular Adhesion Molecule-1IntestinesKupffer CellsLiverLiver TransplantationMaleMembrane Transport ProteinsMetagenomeGlycoproteinsIntercellular Adhesion Molecule-1LYVE1 protein, mouseMembrane Transport ProteinsReceptors, Pattern Recognition

Identifiers

PMID23159949
PMCPMC3532712
OpenAlexW2128109029

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.