Evidence map›Paper›PMID 38834554›Full record

ArticleLight, science & applications2024

Deformable microlaser force sensing.

Eleni Dalaka, Joseph S Hill, Jonathan H H Booth, Anna Popczyk, Stefan R Pulver, Malte C Gather, Marcel Schubert

Abstract read
In one paragraph

Article in Light, science & applications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Stress transmission towards the nucleus of the cell.Frontiers in cell and developmental biology · 2026
    Review
  6. Article
  7. 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.

Eleni Dalaka *Centre of Biophotonics, SUPA, School of Physics and Astronomy, University of St Andrews, North Haugh, St Andrews, UK.ORCID http://orcid.org/0000-0003-3306-7466
Joseph S Hill *Centre of Biophotonics, SUPA, School of Physics and Astronomy, University of St Andrews, North Haugh, St Andrews, UK.
Jonathan H H BoothHumboldt Centre for Nano- and Biophotonics, Department of Chemistry, University of Cologne, Köln, Germany.
Anna PopczykHumboldt Centre for Nano- and Biophotonics, Department of Chemistry, University of Cologne, Köln, Germany.
Stefan R PulverSchool of Psychology and Neuroscience, University of St Andrews, St Mary's Quad, South Street, St Andrews, UK.
Malte C GatherCentre of Biophotonics, SUPA, School of Physics and Astronomy, University of St Andrews, North Haugh, St Andrews, UK. malte.gather@uni-koeln.de.ORCID http://orcid.org/0000-0002-4857-5562
Marcel SchubertHumboldt Centre for Nano- and Biophotonics, Department of Chemistry, University of Cologne, Köln, Germany. marcel.schubert@uni-koeln.de.ORCID http://orcid.org/0000-0002-8739-4852

Funding

Alexander von Humboldt-Stiftung (Alexander von Humboldt Foundation) AvH ProfessorshipDeutsche Forschungsgemeinschaft (German Research Foundation) INST 216/1120-1 FUGGEC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 640012EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) (FP/2014-2020RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/P030017/1Royal Society DH160102Royal Society RGF\EA\180051)
6 · The paper itself

Abstract

Mechanical forces are key regulators of cellular behavior and function, affecting many fundamental biological processes such as cell migration, embryogenesis, immunological responses, and pathological states. Specialized force sensors and imaging techniques have been developed to quantify these otherwise invisible forces in single cells and in vivo. However, current techniques rely heavily on high-resolution microscopy and do not allow interrogation of optically dense tissue, reducing their application to 2D cell cultures and highly transparent biological tissue. Here, we introduce DEFORM, deformable microlaser force sensing, a spectroscopic technique that detects sub-nanonewton forces with unprecedented spatio-temporal resolution. DEFORM is based on the spectral analysis of laser emission from dye-doped oil microdroplets and uses the force-induced lifting of laser mode degeneracy in these droplets to detect nanometer deformations. Following validation by atomic force microscopy and development of a model that links changes in laser spectrum to applied force, DEFORM is used to measure forces in 3D and at depths of hundreds of microns within tumor spheroids and late-stage Drosophila larva. We furthermore show continuous force sensing with single-cell spatial and millisecond temporal resolution, thus paving the way for non-invasive studies of biomechanical forces in advanced stages of embryogenesis, tissue remodeling, and tumor invasion.

Identifiers

PMID38834554
PMCPMC11150448

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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.