Evidence map›Paper›PMID 41579865›Full record

ArticleCell reports methods2026

Fluorescent indicators for visualizing dynamic contact between cells and between processes originating from a single cell.

Takashi Kanadome, Natsumi Hoshino, Susumu Jitsuki, Hidehiko Hashimoto, Takeshi Yagi, Takeharu Nagai

Abstract read
In one paragraph

Article in Cell reports methods, 2026. 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

6 authors.

Takashi KanadomePrecursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), Kawaguchi, Saitama 332-0012, Japan; Laboratory of Neuronal Cell Biology, National Institute for Basic Biology, Okazaki, Aichi 444-8787, Japan; Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan; Department of Basic Biology, Graduate University for Advanced Studies (SOKENDAI), Okazaki, Aichi 444-8787, Japan; Research Core, Mie University, Tsu, Mie 514-8507, Japan; SANKEN, The University of Osaka, 8-1 Mihogaoka, Ibaraki, Osaka 567-0047, Japan. Electronic address: kanadome@nibb.ac.jp.
Natsumi HoshinoKOKORO-Biology Group, Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka 565-0871, Japan; Department of Anatomy and Developmental Neurobiology, Graduate School of Biomedical Sciences, Tokushima University, Kuramoto-cho, Tokushima 770-8503, Japan.
Susumu JitsukiDepartment of Biochemistry, Graduate School of Medicine, Mie University, Tsu, Mie 514-8507, Japan.
Hidehiko HashimotoPrecursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), Kawaguchi, Saitama 332-0012, Japan; Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka 565-0871, Japan.
Takeshi YagiKOKORO-Biology Group, Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka 565-0871, Japan.
Takeharu NagaiSANKEN, The University of Osaka, 8-1 Mihogaoka, Ibaraki, Osaka 567-0047, Japan; Trans Dimensional Life Imaging Division, Institute for Open and Transdisciplinary Research Initiative, The University of Osaka, Suita, Osaka 565-0871, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cells continuously communicate through dynamic cell-cell contacts. Tools for visualizing these dynamic interactions in living cells are essential to the study of fundamental biological processes in multicellular organisms. Here, we present two fluorescent indicators, Gachapin and Gachapin-C, for visualizing dynamic cell-cell contact. Gachapin visualizes not only static but also dynamic contacts. Multiplexed imaging combining green Gachapin with spectrally distinct indicators allows simultaneous monitoring of contact dynamics, cytoskeletal assembly, and intracellular signaling during cell movement. Furthermore, the formation and disruption of contacts between neuronal processes can be visualized. Gachapin-C enables contact visualization with a single indicator component, whereas previous indicators required two components introduced into different cells. This feature allows Gachapin-C to monitor contacts between processes originating from a single cell. We expect Gachapin and Gachapin-C will serve as useful tools for providing deeper insights into cell-cell contact-mediated processes.

Indexed as

Cell CommunicationFluorescent DyesSingle-Cell AnalysisAnimalsHumansMicroscopy, FluorescenceNeuronsFluorescent Dyesbioimagingcell-cell contactCP: imagingddGFPfluorescent indicatorneuronal self-recognition

Identifiers

PMID41579865
PMCPMC12946757

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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.