Evidence map›Paper›PMID 41058731›Full record

ArticleSmall science2025

A Microfluidic Platform for Actin-Based Membrane Remodeling Reveals the Stabilizing Role of Branched Actin Networks on Lipid Microdomains.

Lixin Huang, Rogério Lopes Dos Santos, Sid Labdi, Guillaume Lamour, Olek Maciejak, Michel Malo, John Manzi, Martin Lenz, Jacques Fattaccioli, Clément Campillo

Abstract read
In one paragraph

Article in Small science, 2025. 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

10 authors.

Lixin HuangUniversité Paris-Saclay Univ Evry CY Cergy Paris Université CNRS, LAMBE Evry-Courcouronnes 91025 France.
Rogério Lopes Dos SantosUniversité Paris-Saclay Univ Evry CY Cergy Paris Université CNRS, LAMBE Evry-Courcouronnes 91025 France.ORCID https://orcid.org/0000-0002-0524-1095
Sid LabdiUniversité Paris-Saclay Univ Evry CY Cergy Paris Université CNRS, LAMBE Evry-Courcouronnes 91025 France.ORCID https://orcid.org/0000-0003-4247-0206
Guillaume LamourUniversité Paris-Saclay Univ Evry CY Cergy Paris Université CNRS, LAMBE Evry-Courcouronnes 91025 France.ORCID https://orcid.org/0000-0002-9331-5532
Olek MaciejakUniversité Paris-Saclay Univ Evry CY Cergy Paris Université CNRS, LAMBE Evry-Courcouronnes 91025 France.ORCID https://orcid.org/0000-0001-9594-9435
Michel MaloUniversité Paris-Saclay Univ Evry CY Cergy Paris Université CNRS, LAMBE Evry-Courcouronnes 91025 France.ORCID https://orcid.org/0009-0000-8339-513X
John ManziInstitut Curie Université PSL Sorbonne Université CNRS UMR168 Physique des Cellules et Cancer Paris 75005 France.ORCID https://orcid.org/0000-0003-2574-4260
Martin LenzLPTMS, CNRS Université Paris-Sud Université Paris-Saclay Orsay 91405 France.ORCID https://orcid.org/0000-0002-2307-1106
Jacques FattaccioliCPCV, Département de Chimie, École Normale Supérieure PSL University Sorbonne Université, CNRS Paris 75005 France.ORCID https://orcid.org/0000-0002-0095-2576
Clément CampilloUniversité Paris-Saclay Univ Evry CY Cergy Paris Université CNRS, LAMBE Evry-Courcouronnes 91025 France.ORCID https://orcid.org/0000-0003-4698-8643

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell shape changes, essential for processes such as motility or division, are controlled by the actomyosin cortex that actively remodels biological membranes. Their mechanisms can be deciphered in vitro using biomimetic reconstituted systems, such as giant unilamellar vesicles (GUVs) with controlled lipid composition coupled to reconstituted actin networks. These assays allow mimicking cell shape changes in controlled biochemical and biophysical environments. However, studying the dynamics of these shape changes on statistically significant populations of GUVs with the possibility to sequentially modify the protein composition of the assay is a major experimental challenge. To address these issues, a microfluidic approach is used to immobilize several dozens of isolated GUVs and monitor membrane and actin network evolution. The loading of the chamber with GUVs and actin is first characterized. Then, the actin-induced remodeling of populations of homogeneous and phase-separated GUVs is monitored and shows that actin networks prevent the coalescence of lipid microdomains and that, in return, the number of domains affects the actin network structure. This microfluidic-based experimental strategy, thus, allows for studying actin-induced membrane deformation in vitro and can be adapted to other studies on membrane remodeling processes.

Indexed as

actinArp2/3 complexcytoskeletonfluorescence analysisgiant unilamellar vesicleslipid liquid phase‐separationmicrofluidics

Identifiers

PMID41058731
PMCPMC12499385

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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.