Evidence map›Paper›PMID 35435815›Full record

ArticleAutophagy2023

Autophagy profiling in single cells with open source CellProfiler-based image analysis.

David S Schüssele, Patricia K Haller, Maximilian L Haas, Catherine Hunter, Katharina Sporbeck, Tassula Proikas-Cezanne

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2023. 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
3.6field-weighted citation impact, top 6% 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, 24 citations in OpenAlex.

  1. Article
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  4. Article
  5. Interconnections of insulin/IGF-1 signaling and autophagy abnormalities in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
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  7. Article
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  9. Article
  10. Review
  11. Article
  12. Article
  13. IKCell death & disease · 2022
    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 1 country.

David S SchüsseleInterfaculty Institute of Cell Biology, Eberhard Karls University Tübingen, Tübingen, Germany.
Patricia K HallerInterfaculty Institute of Cell Biology, Eberhard Karls University Tübingen, Tübingen, Germany.
Maximilian L HaasInterfaculty Institute of Cell Biology, Eberhard Karls University Tübingen, Tübingen, Germany.
Catherine HunterInterfaculty Institute of Cell Biology, Eberhard Karls University Tübingen, Tübingen, Germany.
Katharina SporbeckInterfaculty Institute of Cell Biology, Eberhard Karls University Tübingen, Tübingen, Germany.
Tassula Proikas-CezanneInterfaculty Institute of Cell Biology, Eberhard Karls University Tübingen, Tübingen, Germany.ORCID 0000-0001-6934-132X
Max Planck Institute for Developmental Biology · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single cell-based analysis of macroautophagy/autophagy is largely achieved through the use of fluorescence microscopy to detect autophagy-related proteins that associate with autophagic membranes and therefore can be quantified as fluorescent puncta. In this context, an automated analysis of the number and size of recognized puncta is preferable to a manual count, because more reliable results can be generated in a short time. Here we present a method for open source CellProfiler software-based analysis for quantitative autophagy assessments using GFP-tagged WIPI1 (WD repeat domain, phosphoinositide interacting 1) images acquired with Airyscan or confocal laser-scanning microscopy. The CellProfiler protocol is provided as a ready-to-use software pipeline, and the creation of this pipeline is detailed in both text and video formats. In addition, we provide CellProfiler pipelines for endogenous SQSTM1/p62 (sequestosome 1) or intracellular lipid droplet (LD) analysis, suitable to assess forms of selective autophagy. All protocols and software pipelines can be quickly and easily adapted for the use of alternative autophagy markers or cell types, and can also be used for high-throughput purposes.

Indexed as

AutophagyPhosphatidylinositolsAutophagy-Related ProteinsAutophagy-Related ProteinsPhosphatidylinositolsAiryscan microscopyautophagyCellProfilerlipid dropletsSQSTM1/p62WIPI1

Identifiers

PMID35435815
PMCPMC9809960
OpenAlexW4224249234

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.