Evidence map›Paper›PMID 40620762›Full record

ArticleFrontiers in cell and developmental biology2025

Fabrication of microcompartments with controlled size and shape for encapsulating active matter.

Benoit Vianay, Christophe Guérin, Laurène Gressin, Magali Orhant-Prioux, Laurent Blanchoin, Manuel Théry, Alexandra Colin

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Mimicking Cellular Membranes With Micropatterned Lipid Bilayers.Chemphyschem : a European journal of chemical physics and physical chemistry · 2026
    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

7 authors.

Benoit VianayCytoMorphoLab LPCV, UMR 5168, CEA, CNRS, INRA, Interdisciplinary Research Institute of Grenoble, University Grenoble-Alpes, Grenoble, France.
Christophe GuérinCytoMorphoLab LPCV, UMR 5168, CEA, CNRS, INRA, Interdisciplinary Research Institute of Grenoble, University Grenoble-Alpes, Grenoble, France.
Laurène GressinCytoMorphoLab LPCV, UMR 5168, CEA, CNRS, INRA, Interdisciplinary Research Institute of Grenoble, University Grenoble-Alpes, Grenoble, France.
Magali Orhant-PriouxCytoMorphoLab LPCV, UMR 5168, CEA, CNRS, INRA, Interdisciplinary Research Institute of Grenoble, University Grenoble-Alpes, Grenoble, France.
Laurent BlanchoinCytoMorphoLab LPCV, UMR 5168, CEA, CNRS, INRA, Interdisciplinary Research Institute of Grenoble, University Grenoble-Alpes, Grenoble, France.
Manuel ThéryCytoMorphoLab LPCV, UMR 5168, CEA, CNRS, INRA, Interdisciplinary Research Institute of Grenoble, University Grenoble-Alpes, Grenoble, France.
Alexandra ColinCytoMorphoLab LPCV, UMR 5168, CEA, CNRS, INRA, Interdisciplinary Research Institute of Grenoble, University Grenoble-Alpes, Grenoble, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In all living systems, the cytoplasm is separated from the external environment by membranes. This confinement imposes spatial constraints on the self-organization of internal components, filaments and organelles. While reconstituted systems are instrumental for understanding fundamental biological principles, traditional experiments often utilize volumes vastly larger than actual cells. In recent studies, water-in-oil droplets or giant unilamellar vesicles have been widely used to impose confinement. However, these compartments present imaging challenges and make precise protein content control difficult. To address these limitations, we have developed versatile microwells that are straightforward to implement, compatible with different types of imaging and suitable for long-term experiments. These microwells are compatible with several surface treatments and a wide range of experimental techniques making them a powerful tool for answering key questions in cell biology. We present here a detailed protocol of the fabrication of the microwells as well as characterization of the method to ensure quality throughout the manufacturing process. These microwells support various cytoskeleton-based processes including actin polymerization, dynamic steady-state actin networks, and composite actin-microtubule networks. More broadly, they can be used to encapsulate and study over time any kind of active matter.

Indexed as

active mattercompartmentscytoskeletonlipidsmicrochambersmicrofabricationmicrowells

Identifiers

PMID40620762
PMCPMC12226457

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.