Evidence map›Paper›PMID 30486423›Full record

ArticleInternational journal of molecular sciences2018

Differential Effects of Posttranslational Modifications of CXCL8/Interleukin-8 on CXCR1 and CXCR2 Internalization and Signaling Properties.

Alessandro Vacchini, Anneleen Mortier, Paul Proost, Massimo Locati, Mieke Metzemaekers, Elena Monica Borroni

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Construction of a diagnostic model based on random forest and artificial neural network for peri-implantitis.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. The immunological function of CXCR2 in the liver during sepsis.Journal of inflammation (London, England) · 2022
    Review
  10. Dual FunctionalizedFrontiers in bioengineering and biotechnology · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. 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

6 authors at 2 institutions in 2 countries.

Alessandro VacchiniHumanitas Clinical and Research Center, via Manzoni 56, 20089 Rozzano, Milan, Italy. alessandro.vacchini@outlook.com.
Anneleen MortierLaboratory of Molecular Immunology, Department of Microbiology and Immunology, Rega Institute for Medical Research, KU Leuven, Herestraat 49 box 1042, B-3000 Leuven, Belgium. anneleen_mortier@hotmail.com.
Paul ProostLaboratory of Molecular Immunology, Department of Microbiology and Immunology, Rega Institute for Medical Research, KU Leuven, Herestraat 49 box 1042, B-3000 Leuven, Belgium. paul.proost@kuleuven.be.ORCID 0000-0002-0133-5545
Massimo LocatiHumanitas Clinical and Research Center, via Manzoni 56, 20089 Rozzano, Milan, Italy. Massimo.Locati@humanitasresearch.it.
Mieke MetzemaekersLaboratory of Molecular Immunology, Department of Microbiology and Immunology, Rega Institute for Medical Research, KU Leuven, Herestraat 49 box 1042, B-3000 Leuven, Belgium. mieke.metzemaekers@kuleuven.be.
Elena Monica BorroniHumanitas Clinical and Research Center, via Manzoni 56, 20089 Rozzano, Milan, Italy. Elena.Borroni@humanitasresearch.it.
Humanitas University · ITRega Institute for Medical Research · BE

Funding

Fonds Wetenschappelijk Onderzoek G.0808.18N and G.0D25.17NFonds Wetenschappelijk Onderzoek postdoctoral fellowshipHercules Foundation Flanders AKUL/11/31L'Oréal-Unesco Belgilux - FWO-Vlaanderen PhD fellowship
6 · The paper itself

Abstract

CXCL8 or interleukin (IL)-8 directs neutrophil migration and activation through interaction with CXCR1 and CXCR2 that belong to the family of G protein-coupled receptors (GPCRs). Naturally occurring posttranslational modifications of the NH₂-terminal region of CXCL8 affect its biological activities, but the underlying molecular mechanisms are only partially understood. Here, we studied the implications of site-specific citrullination and truncation for the signaling potency of CXCL8. Native CXCL8(1-77), citrullinated [Cit5]CXCL8(1-77) and the major natural isoform CXCL8(6-77) were chemically synthesized and tested in internalization assays using human neutrophils. Citrullinated and truncated isoforms showed a moderately enhanced capacity to induce internalization of CXCR1 and CXCR2. Moreover, CXCL8-mediated activation of Gα

Indexed as

EndocytosisProtein Processing, Post-TranslationalSignal Transductionbeta-ArrestinsHumansInterleukin-8NeutrophilsProtein BindingProtein Interaction Domains and MotifsProtein TransportReceptors, Interleukin-8AReceptors, Interleukin-8Bbeta-ArrestinsInterleukin-8Receptors, Interleukin-8AReceptors, Interleukin-8BchemokineCXCL8G protein-coupled receptorposttranslational modifications

Identifiers

PMID30486423
PMCPMC6321254
OpenAlexW2903163876

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.