Högskolan i Skövde

his.sePublications
System disruptions
We are currently experiencing disruptions on the search portals due to high traffic. We are working to resolve the issue, you may temporarily encounter an error message.
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • apa-cv
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Exposing kinetic disparities between inflammasome readouts using time-resolved analysis
University of Skövde, School of Bioscience. University of Skövde, Systems Biology Research Environment. School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Sweden ; Inflammatory Response and Infection Susceptibility Centre (iRiSC), Örebro University, Sweden. (Infection Biology)ORCID iD: 0000-0003-3124-5062
School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Sweden ; Inflammatory Response and Infection Susceptibility Centre (iRiSC), Örebro University, Sweden.
University of Skövde, School of Bioscience. University of Skövde, Systems Biology Research Environment. Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, Göteborg University, Sweden. (Infection Biology)
Nanoxis Consulting AB, Göteborg, Sweden ; Department of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, Göteborg University, Sweden ; Department of Clinical Microbiology, Sahlgrenska University Hospital, Region Västra Götaland, Göteborg, Sweden.
Show others and affiliations
2024 (English)In: Heliyon, E-ISSN 2405-8440, Vol. 10, no 11, article id e32023Article in journal (Refereed) Published
Abstract [en]

The NLRP3 inflammasome is an intracellular multiprotein complex described to be involved in both an effective host response to infectious agents and various diseases. Investigation into the NLRP3 inflammasome has been extensive in the past two decades, and often revolves around the analysis of a few specific readouts, including ASC-speck formation, caspase-1 cleavage or activation, and cleavage and release of IL-1β and/or IL-18. Quantification of these readouts is commonly undertaken as an endpoint analysis, where the presence of each positive outcome is assessed independently of the others. In this study, we apply time-resolved analysis of a human macrophage model (differentiated THP-1-ASC-GFP cells) to commonly accessible methods. This approach yields the additional quantifiable metrics time-resolved absolute change and acceleration, allowing comparisons between readouts. Using this methodological approach, we reveal (potential) discrepancies between inflammasome-related readouts that otherwise might go undiscovered. The study highlights the importance of time-resolved data in general and may be further extended as well as incorporated into other areas of research. 

Place, publisher, year, edition, pages
Elsevier, 2024. Vol. 10, no 11, article id e32023
Keywords [en]
ASC-Specks, Cell response, Cytokines, Human macrophages, LDH leakage, Live-cell imaging, NLRP3 inflammasome, THP-1 cells
National Category
Biomedical Laboratory Science/Technology Bioinformatics and Computational Biology Pharmaceutical and Medical Biotechnology Cell and Molecular Biology
Research subject
Infection Biology
Identifiers
URN: urn:nbn:se:his:diva-23919DOI: 10.1016/j.heliyon.2024.e32023ISI: 001251271000001PubMedID: 38867997Scopus ID: 2-s2.0-85194572795OAI: oai:DiVA.org:his-23919DiVA, id: diva2:1866342
Funder
Knowledge Foundation, 20200017Knowledge Foundation, 20160044
Note

CC BY 4.0

© 2024 The Author(s)

Correspondence Address: M. Herring; School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden; email: Matthew.herring@oru.se

We acknowledge scientific support from the Exploring Inflammation in Health and Disease (X-HiDE) Consortium, which is a strategic research profile at Örebro University funded by the Knowledge Foundation (20200017; 20160044). We also acknowledge the Centre for Cellular Imaging at the University of Gothenburg and the National Microscopy Infrastructure, NMI (VR-RFI 2019-00217) for providing advice and assistance in live-cell imaging.

Available from: 2024-06-07 Created: 2024-06-07 Last updated: 2025-02-26Bibliographically approved

Open Access in DiVA

fulltext(5259 kB)1193 downloads
File information
File name FULLTEXT01.pdfFile size 5259 kBChecksum SHA-512
8d239d6c8660d210801028533c861eeb995138dca0aa3d6b08b87aabd1d6955c4f0f43ceb8172b645dc30f7c5b7048970dc3f3558f7cdb42ec7556d23ce7ba6a
Type fulltextMimetype application/pdf

Other links

Publisher's full textPubMedScopus

Authority records

Herring, MatthewPotter, RyanEjdebäck, Mikael

Search in DiVA

By author/editor
Herring, MatthewPotter, RyanEjdebäck, Mikael
By organisation
School of BioscienceSystems Biology Research Environment
In the same journal
Heliyon
Biomedical Laboratory Science/TechnologyBioinformatics and Computational BiologyPharmaceutical and Medical BiotechnologyCell and Molecular Biology

Search outside of DiVA

GoogleGoogle Scholar
Total: 1193 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 1508 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • apa-cv
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf