Evidence map›Paper›PMID 42129123›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Monitoring Inflammasome Activity Through ASC Speck Formation in THP-1 ASC-GFP Cells.

Timothy Muusse, Sarah Little

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Timothy MuusseBiomedical Manufacturing, Commonwealth Scientific and Industrial Research Organisation (CSIRO), Clayton, VIC, Australia. timothymuusse@gmail.com.
Sarah LittleBiomedical Manufacturing, Commonwealth Scientific and Industrial Research Organisation (CSIRO), Clayton, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammasome activation and signaling are hallmarks of immune activation and cellular response. Understanding the complex mechanisms involved in the formation of the NLRP3 inflammasome is vital to accurately evaluating potentially anti-inflammatory molecules. The oligomerization of ASC is a well-documented indicator of inflammasome activation, and ASC-GFP allows the visualization of these "specks." Here, we detail a higher throughput methodology for monitoring inflammasome activation and screening potential anti-inflammatory compounds utilizing an Incucyte® live cell imager. It provides a platform to observe cell activation and cell death in real-time. Cells can be visualized from initial plating through to inflammasome-induced cell death, granting insights into inflammasome activation kinetics and previously unknown toxicities.

Indexed as

CARD Signaling Adaptor ProteinsGreen Fluorescent ProteinsInflammasomesHumansNLR Family, Pyrin Domain-Containing 3 ProteinTHP-1 CellsCARD Signaling Adaptor ProteinsGreen Fluorescent ProteinsInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinPYCARD protein, humanAnti-inflammatoryASCIncucyte®InflammasomeTHP-1 cells

Identifiers

What OpenQuestion holds

Textmetadata
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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.