Evidence map›Paper›PMID 29670923›Full record

ArticleJournal of immunology research2018

Cathelicidin LL-37 Affects Surface and Intracellular Toll-Like Receptor Expression in Tissue Mast Cells.

Justyna Agier, Ewa Brzezińska-Błaszczyk, Paulina Żelechowska, Magdalena Wiktorska, Jacek Pietrzak, Sylwia Różalska

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

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  17. Rational Design of Immunomodulatory Hydrogels for Chronic Wound Healing.Advanced materials (Deerfield Beach, Fla.) · 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

6 authors at 2 institutions in 1 country.

Justyna AgierDepartment of Experimental Immunology, Faculty of Health Sciences, Medical University of Lodz, Lodz, Poland.
Ewa Brzezińska-BłaszczykDepartment of Experimental Immunology, Faculty of Health Sciences, Medical University of Lodz, Lodz, Poland.ORCID 0000-0002-1466-4321
Paulina ŻelechowskaDepartment of Experimental Immunology, Faculty of Health Sciences, Medical University of Lodz, Lodz, Poland.ORCID 0000-0001-6626-3215
Magdalena WiktorskaDepartment of Molecular Cell Mechanisms, Faculty of Health Sciences, Medical University of Lodz, Lodz, Poland.
Jacek PietrzakDepartment of Pharmaceutical Biochemistry and Molecular Diagnostics, Faculty of Pharmacy, Medical University of Lodz, Lodz, Poland.
Sylwia RóżalskaDepartment of Industrial Microbiology and Biotechnology, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
Medical University of Lodz · PLUniversity of Łódź · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Undoubtedly, mast cells take part in host defense against microorganisms as they are numerous at the portal of infection, they release many proinflammatory and antimicrobial mediators, and they express pattern recognition receptors, such as TLRs. These receptors play a key role in recognition and binding molecules associated with microorganisms and molecules associated with damage. Cathelicidins exhibit direct antimicrobial activities against a broad spectrum of microbes by perturbing their cell membranes. Accumulating evidence suggests a role for these molecules in supporting cell activation. We examined the impact of human cathelicidin LL-37 on tissue mast cell TLR expression and distribution. Depending on context, we show that LL-37 stimulation resulted in minor to major effects on TLR2, TLR3, TLR4, TLR5, TLR7, and TLR9 expression. Confocal microscopy analysis showed that, upon stimulation, TLRs may translocate from the cell interior to the surface and conversely. FPR2 and EGFR inhibitors reduced the increase in expression of selected receptors. We also established that LL-37 acts as a powerful inducer of CCL3 and ROS generation. These results showed that in response to LL-37, mast cells enhance the capability to detect invading pathogens by modulation of TLR expression in what may be involved FPR2 or EGFR molecules.

Indexed as

Antimicrobial Cationic PeptidesCathelicidinsCells, CulturedChemokine CCL3ErbB ReceptorsHumansImmunity, InnateInfectionsIntracellular SpaceMast CellsMicroscopy, ConfocalProtein TransportReactive Oxygen SpeciesReceptors, Formyl PeptideReceptors, LipoxinToll-Like ReceptorsAntimicrobial Cationic PeptidesCathelicidinsChemokine CCL3EGFR protein, humanErbB ReceptorsFPR2 protein, humanReactive Oxygen SpeciesReceptors, Formyl PeptideReceptors, LipoxinToll-Like Receptors

Identifiers

PMID29670923
PMCPMC5836302
OpenAlexW2790646706

What OpenQuestion holds

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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.