Evidence map›Paper›PMID 40606011›Full record

ArticleFrontiers in systems neuroscience2025

Toward a role for the acoustic field in cells interaction.

Marco Girasole, Pier Francesco Moretti, Angela Di Giannatale, Virginia Di Paolo, Angela Galardi, Silvia Lampis, Simone Dinarelli, Giovanni Longo

Abstract read
In one paragraph

Article in Frontiers in systems neuroscience, 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. 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

8 authors.

Marco GirasoleInstitute of Matter Structure, Italian National Research Council, ISM-CNR, Rome, Italy.
Pier Francesco MorettiDepartment of Earth System Sciences and Environmental Technologies, Consiglio Nazionale delle Ricerche, Rome, Italy.
Angela Di GiannataleHematology/Oncology and Cell and Gene Therapy Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Virginia Di PaoloHematology/Oncology and Cell and Gene Therapy Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Angela GalardiHematology/Oncology and Cell and Gene Therapy Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Silvia LampisHematology/Oncology and Cell and Gene Therapy Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Simone DinarelliInstitute of Matter Structure, Italian National Research Council, ISM-CNR, Rome, Italy.
Giovanni LongoInstitute of Matter Structure, Italian National Research Council, ISM-CNR, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoscale motility of cells is a fundamental phenomenon, closely associated with biological status and response to environmental solicitations, whose investigation has disclosed new perspectives for the comprehension of cell behavior and fate. To investigate intracellular interactions, we designed an experiment to monitor movements of clusters of neuroblastoma cells (SH-SY5Y) growing on a nanomechanical oscillator (nanomotion sensor) suspended few hundreds of microns over the surface of a Petri dish where other neuroblastoma cells are freely moving. We observed that the free-to-move cells feel the presence of cells on the nearby nanosensor (at a distance of up to 300 microns) and migrate toward them, even in presence of environmental hampering factors, such as medium microflows. The interaction is bidirectional since, as evidenced by nanomotion sensing, the cells on the sensor enhance their motion when clusters of freely moving cells approach. Considering the geometry and environmental context, our observations extend beyond what can be explained by sensing of chemical trackers, suggesting the presence of other physical mechanisms. We hypothesize that the acoustic field generated by cell vibrations can have a role in the initial recognition between distant clusters. Integrating our findings with a suitable wave propagation model, we show that mechanical waves produced by cellular activity have sufficient energy to trigger mechanotransduction in target cells hundreds of microns away. This interaction can explain the observed distance-dependent patterns of cellular migration and motion alteration. Our results suggest that acoustic fields generated by cells can mediate cell-cell interaction and contribute to signaling and communication.

Indexed as

acoustic fieldcell behaviorcell-cell interactionsmechanical wavesnanomotion sensorneuroblastoma cell

Identifiers

PMID40606011
PMCPMC12213812

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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.