Evidence map›Paper›PMID 39595603›Full record

ArticleBiomolecules2024

Comparison of Different Keratinocyte Cell Line Models for Analysis of NLRP1 Inflammasome Activation.

Tian Wang, Amir S Yazdi, Diana Panayotova-Dimitrova

Abstract readComparative Study
In one paragraph

Article in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

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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

3 citing papers in PubMed.

  1. Review
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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

3 authors.

Tian WangDepartment of Dermatology and Allergology, University Hospital RWTH Aachen, 52074 Aachen, Germany.
Amir S YazdiDepartment of Dermatology and Allergology, University Hospital RWTH Aachen, 52074 Aachen, Germany.
Diana Panayotova-DimitrovaDepartment of Dermatology and Allergology, University Hospital RWTH Aachen, 52074 Aachen, Germany.

Funding

Chinese Scolarship Counsil Stipend N.202208080067German Research Foundation DFG DI 2440/3-1German Research Foundation DFG FOR 2497 PEGASUS Ya-182/4START-Program, Faculty of Medicine RWTH University Aachen Az. 57/22
6 · The paper itself

Abstract

The NLRP1 (nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing-1) inflammasome is the most important inflammasome in human keratinocytes. It plays a crucial role in regulating innate immunity in the skin. This study aimed to evaluate NLRP1 inflammasome activation and the corresponding levels of detection in different keratinocyte cell lines to identify a suitable in vitro model for analyzing inflammasome activation in keratinocytes. We compared NLRP1 inflammasome activation, expression, and cell death among primary keratinocytes and immortalized keratinocyte cell lines HaCaT, HaSKpw, and SVTERT upon stimulation with ultraviolet B (UVB) irradiation or talabostat. The effects of both NLRP1 inducers on cell death and the modification of NLRP1 molecules were examined using fluorescence-activated cell sorting analysis, Western blotting, and an enzyme-linked immunosorbent assay. The key inflammasome components had varied expression levels among the keratinocyte cell models, with the highest expression observed in primary keratinocytes. Moreover, our data showed that both UVB and talabostat triggered cell death, and NLRP1 inflammasome activation was readily detected in primary keratinocytes but not in the analyzed immortalized keratinocyte cell lines. Therefore, we do not recommend the use of the immortalized keratinocyte cell lines HaCaT, HaSKpw, and SVTERT for analyzing inflammasome activation in keratinocytes; we strongly recommend the use of primary keratinocytes for these studies.

Indexed as

InflammasomesKeratinocytesNLR ProteinsUltraviolet RaysAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsCell DeathCell LineHaCaT CellsHumansAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsInflammasomesNLRP1 protein, humanNLR ProteinscytokineskeratinocytesNLRP1 inflammasometalabostatultraviolet B

Identifiers

PMID39595603
PMCPMC11592008

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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.