Evidence map›Paper›PMID 40769969›Full record

ArticleCell death discovery2025

Integrated real-time imaging of executioner caspase dynamics, apoptosis-induced proliferation, and immunogenic cell death using a stable fluorescent reporter platform.

Selen Selcen, Lena Wieland, Tiago De Oliveira, Michael Ghadimi, Lena-Christin Conradi, Günter Schneider, Leonie Witte, Matthias Wirth

Abstract read
In one paragraph

Article in Cell death discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

8 authors.

Selen SelcenDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.ORCID http://orcid.org/0009-0006-4006-4369
Lena WielandDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.ORCID http://orcid.org/0009-0006-5969-1012
Tiago De OliveiraDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.ORCID http://orcid.org/0000-0002-2502-7897
Michael GhadimiDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Lena-Christin ConradiDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Günter SchneiderDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.ORCID http://orcid.org/0000-0003-1840-4508
Leonie Witte *Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.ORCID http://orcid.org/0000-0003-2154-937X
Matthias Wirth *Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany. matthias.wirth@med.uni-goettingen.de.ORCID http://orcid.org/0000-0002-8340-0872

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) WI 6148/1-1, 529255113Deutsche Krebshilfe (German Cancer Aid) 70115444Wilhelm Sander-Stiftung (Wilhelm Sander Foundation) 2017.048.2
6 · The paper itself

Abstract

Regulated cell death plays a central role in tissue homeostasis, disease progression, and therapeutic responses. However, tools to study these processes with high spatiotemporal resolution in physiologically relevant systems remain limited. Here, we present a fluorescent reporter cell system that enables real-time visualization of caspase-3/-7 activity via a DEVD-based biosensor, alongside a constitutive fluorescent marker for assessing successful transduction and cell presence. We generated stable cell lines expressing this reporter and adapted them to both 2D and 3D culture systems, including organoids. This platform allowed dynamic tracking of apoptotic events and viability loss at single-cell resolution. Using a proliferation dye, we also detected apoptosis-induced proliferation in neighboring cells. Furthermore, the system enabled simultaneous detection of immunogenic cell death via an endpoint measurement of surface calreticulin exposure by flow cytometry, supporting its application in studying immunogenic signaling. By measuring and integrating multiple cell death readouts by live-cell imaging, our system is well-suited for high-content screening and mechanistic dissection of different modes of cell death. When combined with complementary markers of pyroptosis and necroptosis, this platform may also be extended to investigate more complex, integrated forms of cell death.

Identifiers

PMID40769969
PMCPMC12328661

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Registered trials

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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.