Evidence map›Paper›PMID 40212066›Full record

ArticleSmall science2024

Tuning the Immune Cell Response through Surface Nanotopography Engineering.

Raïssa Rathar, David Sanchez-Fuentes, Hugo Lachuer, Valentin Meire, Aude Boulay, Rudy Desgarceaux, Fabien P Blanchet, Adrian Carretero-Genevrier, Laura Picas

Abstract read
In one paragraph

Article in Small science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors.

Raïssa RatharInstitut de Recherche en Infectiologie de Montpellier (IRIM) Université de Montpellier CNRS UMR 9004 Montpellier 34000 France.ORCID https://orcid.org/0000-0001-8766-2186
David Sanchez-FuentesInstitut d'Électronique et des Systèmes (IES) Université de Montpellier CNRS UMR 5214 Montpellier 34000 France.ORCID https://orcid.org/0000-0003-3208-7238
Hugo LachuerCNRS Université de Paris Institut Jacques Monod 75013 Paris France.ORCID https://orcid.org/0000-0001-9090-7893
Valentin MeireInstitut de Recherche en Infectiologie de Montpellier (IRIM) Université de Montpellier CNRS UMR 9004 Montpellier 34000 France.
Aude BoulayInstitut de Recherche en Infectiologie de Montpellier (IRIM) Université de Montpellier CNRS UMR 9004 Montpellier 34000 France.
Rudy DesgarceauxInstitut d'Électronique et des Systèmes (IES) Université de Montpellier CNRS UMR 5214 Montpellier 34000 France.
Fabien P BlanchetInstitut de Recherche en Infectiologie de Montpellier (IRIM) Université de Montpellier CNRS UMR 9004 Montpellier 34000 France.ORCID https://orcid.org/0000-0003-3168-0697
Adrian Carretero-GenevrierInstitut d'Électronique et des Systèmes (IES) Université de Montpellier CNRS UMR 5214 Montpellier 34000 France.ORCID https://orcid.org/0000-0003-0488-9452
Laura PicasInstitut de Recherche en Infectiologie de Montpellier (IRIM) Université de Montpellier CNRS UMR 9004 Montpellier 34000 France.ORCID https://orcid.org/0000-0002-5619-5228

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) are central regulators of the immune response by detecting inflammatory signals, aberrant cells, or pathogens. DC-mediated immune surveillance requires morphology changes to adapt to the physical and biochemical cues of the external environment. These changes are assisted by a dynamic actin cytoskeleton-membrane interface connected to surface receptors that will trigger signaling cascades. In recent years, the development of synthetic immune environments has allowed to investigate the impact of the external environment in the immune cell response. In this direction, the bioengineering of functional topographical features should make it possible to establish how membrane morphology modulates specific cellular functions in DCs. Herein, the engineering of one-dimensional nanostructured SiO2 surfaces by soft-nanoimprint lithography to manipulate the membrane morphology of ex vivo human DCs is reported. Super-resolution microscopy and live-cell imaging studies show that vertical pillar topographies promote the patterning and stabilization of adhesive actin-enriched structures in DCs. Furthermore, vertical topographies stimulate the spatial organization of innate immune receptors and regulate the Syk- and ERK-mediated signaling pathways across the cell membrane. In conclusion, engineered SiO

Indexed as

actin organizationdendritic cellsmembrane remodelingnanoimprint lithographynanostructured surfacessol–gel chemistry

Identifiers

PMID40212066
PMCPMC11935051

What OpenQuestion holds

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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.