Evidence map›Paper›PMID 36800388›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Spatial organization of lysosomal exocytosis relies on membrane tension gradients.

Hugo Lachuer, Laurent Le, Sandrine Lévêque-Fort, Bruno Goud, Kristine Schauer

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Mechanical forces stimulate Golgi export.The Journal of cell biology · 2026
    Article
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  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Lysosome quality control in health and neurodegenerative diseases.Cellular & molecular biology letters · 2024
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Spatial organization of lysosomal exocytosis relies on membrane tension gradients.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

5 authors.

Hugo LachuerInstitut Curie, Paris Sciences et Lettres Research University, CNRS UMR 144 Cell Biology and Cancer, 75005 Paris, France.ORCID 0000-0001-9090-7893
Laurent LeUniversité Paris-Saclay, CNRS, Institut des Sciences Moléculaires d'Orsay 91405, Orsay, France.ORCID 0000-0002-0487-7729
Sandrine Lévêque-FortUniversité Paris-Saclay, CNRS, Institut des Sciences Moléculaires d'Orsay 91405, Orsay, France.ORCID 0000-0002-9218-3363
Bruno GoudInstitut Curie, Paris Sciences et Lettres Research University, CNRS UMR 144 Cell Biology and Cancer, 75005 Paris, France.ORCID 0000-0003-1227-4159
Kristine SchauerInstitut Curie, Paris Sciences et Lettres Research University, CNRS UMR 144 Cell Biology and Cancer, 75005 Paris, France.ORCID 0000-0002-6102-8790

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lysosomal exocytosis is involved in many key cellular processes but its spatiotemporal regulation is poorly known. Using total internal reflection fluorescence microscopy (TIRFM) and spatial statistics, we observed that lysosomal exocytosis is not random at the adhesive part of the plasma membrane of RPE1 cells but clustered at different scales. Although the rate of exocytosis is regulated by the actin cytoskeleton, neither interfering with actin or microtubule dynamics by drug treatments alters its spatial organization. Exocytosis events partially co-appear at focal adhesions (FAs) and their clustering is reduced upon removal of FAs. Changes in membrane tension following a hypo-osmotic shock or treatment with methyl-β-cyclodextrin were found to increase clustering. To investigate the link between FAs and membrane tension, cells were cultured on adhesive ring-shaped micropatterns, which allow to control the spatial organization of FAs. By using a combination of TIRFM and fluorescence lifetime imaging microscopy (FLIM), we revealed the existence of a radial gradient in membrane tension. By changing the diameter of micropatterned substrates, we further showed that this gradient as well as the extent of exocytosis clustering can be controlled. Together, our data indicate that the spatial clustering of lysosomal exocytosis relies on membrane tension patterning controlled by the spatial organization of FAs.

Indexed as

Cell Physiological PhenomenaExocytosisCell MembraneLysosomesMembranesexocytosisfocal adhesionsmembrane tensionRipley's K functionVamp7

Identifiers

PMID36800388
PMCPMC9974462

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.