Evidence map›Paper›PMID 26511058›Full record

ArticleInnate immunity2016

Modulation of host defense peptide-mediated human mast cell activation by LPS.

Kshitij Gupta, Hariharan Subramanian, Hydar Ali

Open access · greenAbstract read
In one paragraph

Article in Innate immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 44 citations in OpenAlex.

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  18. Angiogenic Host Defense Peptide AG-30/5C and Bradykinin BJournal of immunology (Baltimore, Md. : 1950) · 2019
    Article
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  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

3 authors at 1 institution in 1 country.

Kshitij GuptaDepartment of Pathology, University of Pennsylvania School of Dental Medicine, Philadelphia, PA, USA.
Hariharan SubramanianDepartment of Pathology, University of Pennsylvania School of Dental Medicine, Philadelphia, PA, USA.
Hydar AliDepartment of Pathology, University of Pennsylvania School of Dental Medicine, Philadelphia, PA, USA alih@upenn.edu.
University of Pennsylvania · US

Funding

A novel role for the adapter molecule NHERF1 in regulating asthma and allergic reR00HL121073 · NHLBI · MICHIGAN STATE UNIVERSITY · PI SUBRAMANIAN, HARIHARAN · 2016 to 2018
$734k
Human mast cell-specific Mas-related Gene-X2 (MrgX2) in Anaphylaxis and AsthmaR21AI108585 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALI, HYDAR · 2014 to 2015
$440k
A novel role for the adapter molecule NHERF1 in regulating asthma and allergic reK99HL121073 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SUBRAMANIAN, HARIHARAN · 2014 to 2015
$216k
NHLBI NIH HHS K99 HL121073NHLBI NIH HHS K99-HL121073NHLBI NIH HHS R00 HL121073NIAID NIH HHS AI108585NIAID NIH HHS R21 AI108585
6 · The paper itself

Abstract

Human β-defensin3 (hBD3) and the cathelicidin LL-37 are host defense peptides (HDPs) that directly kill microbes and display immunomodulatory/wound-healing properties via the activation of chemokine, formylpeptide and epidermal growth factor receptors on leukocytes and epithelial cells. A C-terminal 14 amino acid hBD3 peptide with all Cys residues replaced with Ser (CHRG01) and an LL-37 peptide consisting of residues 17-29 (FK-13) display antimicrobial activity but lack immunomodulatory property. Surprisingly, we found that CHRG01 and FK-13 caused Ca(2+) mobilization and degranulation in human mast cells via a novel G protein-coupled receptor known as Mas-related gene-X2 (MrgX2). At local sites of bacterial infection, the negatively charged LPS likely interacts with cationic HDPs to inhibit their activity and thus providing a mechanism for pathogens to escape host defense mechanisms. We found that LPS caused almost complete inhibition of hBD3 and LL-37-induced Ca(2+) mobilization and mast cell degranulation. In contrast, it had no effect on CHRG01 and FK-13-induced mast cell responses. These findings suggest that HDP derivatives that kill microbes, harness mast cell's host defense and wound-healing properties via the activation of MrgX2 but are resistant to inhibition by LPS could be utilized for the treatment of antibiotic-resistant microbial infections.

Indexed as

AnimalsAntimicrobial Cationic Peptidesbeta-DefensinsCalcium SignalingCathelicidinsCell DegranulationCell Line, TumorHumansImmunomodulationLipopolysaccharidesMast CellsMutationNerve Tissue ProteinsRatsReceptors, G-Protein-CoupledReceptors, NeuropeptideAntimicrobial Cationic Peptidesbeta-DefensinsCathelicidinsDEFB103A protein, humanLipopolysaccharidesMRGPRX2 protein, humanNerve Tissue ProteinsReceptors, G-Protein-CoupledReceptors, NeuropeptideHost defense peptidesLPSMas-related gene-X2 (MrgX2)mast cell

Identifiers

PMID26511058
PMCPMC4858174
OpenAlexW1825782952

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.