Evidence map›Paper›PMID 26912318›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Macrophage Galactose-Type Lectin-1 Deficiency Is Associated with Increased Neutrophilia and Hyperinflammation in Gram-Negative Pneumonia.

Christopher N Jondle, Atul Sharma, Tanner J Simonson, Benjamin Larson, Bibhuti B Mishra, Jyotika Sharma

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 24 citations in OpenAlex.

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  12. ASGR1 and Its Enigmatic Relative, CLEC10A.International journal of molecular sciences · 2020
    Review
  13. Regulation of neutrophil function by selective targeting of glycan epitopes expressed on the integrin CD11b/CD18.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  14. Article
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  18. Oxidant sensor cation channel TRPM2 regulates neutrophil extracellular trap formation and protects against pneumoseptic bacterial infection.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  19. Article
  20. 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 1 institution in 1 country.

Christopher N JondleDepartment of Basic Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202.
Atul SharmaDepartment of Basic Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202.
Tanner J SimonsonDepartment of Basic Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202.
Benjamin LarsonDepartment of Basic Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202.ORCID http://orcid.org/0000-0002-1940-9565
Bibhuti B MishraDepartment of Basic Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202.
Jyotika SharmaDepartment of Basic Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202 jyotika.sharma@med.und.edu.
University of North Dakota · US

Funding

Molecular mechanism of Mincle mediated NET formation:Implications for pneumonic sepsisR01AI121804 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHARMA, JYOTIKA · 2016 to 2020
$2.0M
Identification of protective proteins of Francisella using a novel comparative imR21AI107457 · NIAID · UNIVERSITY OF NORTH DAKOTA · PI SHARMA, JYOTIKA · 2014 to 2015
$388k
NIAID NIH HHS R01 AI121804NIAID NIH HHS R01AI121804NIAID NIH HHS R21 AI107457NIAID NIH HHS R21AI107457
6 · The paper itself

Abstract

C-type lectin receptors (CLRs), the carbohydrate-recognizing molecules, orchestrate host immune response in homeostasis and in inflammation. In the present study we examined the function of macrophage galactose-type lectin-1 (MGL1), a mammalian CLR, in pneumonic sepsis, a deadly immune disorder frequently associated with a nonresolving hyperinflammation. In a murine model of pneumonic sepsis using pulmonary infection with Klebsiella pneumoniae, the expression of MGL1 was upregulated in the lungs of K. pneumoniae-infected mice, and the deficiency of this CLR in MGL1(-/-) mice resulted in significantly increased mortality to infection than in the MGL1-sufficient wild-type mice, despite a similar bacterial burden. The phagocytic cells from MGL1(-/-) mice did not exhibit any defects in bacterial uptake and intracellular killing and were fully competent in neutrophil extracellular trap formation, a recently identified extracellular killing modality of neutrophils. Instead, the increased susceptibility of MGL1(-/-) mice seemed to correlate with severe lung pathology, indicating that MGL1 is required for resolution of pulmonary inflammation. Indeed, the MGL1(-/-) mice exhibited a hyperinflammatory response, massive pulmonary neutrophilia, and an increase in neutrophil-associated immune mediators. Concomitantly, MGL1-deficient neutrophils exhibited an increased influx in pneumonic lungs of K. pneumoniae-infected mice. Taken together, these results show a previously undetermined role of MGL1 in controlling neutrophilia during pneumonic infection, thus playing an important role in resolution of inflammation. To our knowledge, this is the first study depicting a protective function of MGL1 in an acute pneumonic bacterial infection.

Indexed as

Adoptive TransferAnimalsAsialoglycoproteinsDisease Models, AnimalExtracellular TrapsGene ExpressionGenetic Predisposition to DiseaseGram-Negative Bacterial InfectionsInflammation MediatorsKlebsiella pneumoniaeLectins, C-TypeLeukocytosisMacrophagesMembrane ProteinsMiceMice, KnockoutAsialoglycoproteinsClec10a protein, mouseInflammation MediatorsLectins, C-TypeMembrane Proteins

Identifiers

PMID26912318
PMCPMC4936400
OpenAlexW2280221229

What OpenQuestion holds

Textmetadata
LicenceTDM
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.