Evidence map›Paper›PMID 39471872›Full record

ArticleJournal of the Royal Society, Interface2024

Long-term tracing of individual human neural cells using multiphoton microscopy and photoconvertible polymer capsules.

Ivan V Smirnov, Veronika S Usatova, Mikhail A Berestovoy, Andrei B Fedotov, Aleksandr A Lanin, Vsevolod V Belousov, Gleb B Sukhorukov

Abstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2024. 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. 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.

Ivan V SmirnovVladimir Zelman Center for Neurobiology and Brain Rehabilitation, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.ORCID 0009-0003-2070-9076
Veronika S UsatovaFederal Center for Brain and Neurotechnologies, Federal Medical-Biological Agency, Moscow 117997, Russia.ORCID 0009-0004-0984-3773
Mikhail A BerestovoyFederal Center for Brain and Neurotechnologies, Federal Medical-Biological Agency, Moscow 117997, Russia.
Andrei B FedotovPhysics Department, Lomonosov Moscow State University, Moscow 119992, Russia.
Aleksandr A LaninPhysics Department, Lomonosov Moscow State University, Moscow 119992, Russia.
Vsevolod V BelousovFederal Center for Brain and Neurotechnologies, Federal Medical-Biological Agency, Moscow 117997, Russia.
Gleb B SukhorukovVladimir Zelman Center for Neurobiology and Brain Rehabilitation, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.

Funding

Brain Program of the IDEAS Research CenterMinistry of Science and Higher Education of the Russian FederationRussian Science Foundation
6 · The paper itself

Abstract

The study of human neural cells, their behaviour and migration are important areas of research in the biomedical field, particularly for potential therapeutic applications. The safety of using neural cells in therapy is still a concern due to a lack of information on long-term changes that may occur. While current methods of cell tracing explore gene manipulations, we elaborate approaches to cell marking with no genetic interference. In this study, we present a novel method for labelling and tracking neural cells using cell-impregnatable photoconvertible polyelectrolyte microcapsules. These capsules demonstrated low cytotoxicity with no effect on the differentiation ability of the neural cells, maintained a high level of fluorescent signal and ability for tracing individual neural cells for over 7 days. The capsules modified with rhodamine- and fluorescein-based dyes were demonstrated to undergo photoconversion by both one- and two-photon lasers while being internalized by neural cells. The finding gives the possibility to select individual capsules inside multicellular structures like spheroids and tissues and alternate their fluorescent appearance. Thus, we can track individual cell paths in complex systems. This new method offers a promising alternative for studying neural cells' long-term behaviour and migration in complex systems such as three-dimensional cellular populations.

Indexed as

NeuronsCapsulesCell TrackingFluorescent DyesHumansMicroscopy, Fluorescence, MultiphotonPolymersCapsulesFluorescent DyesPolymerscell migrationiPSC-derived neural cellslong-term cell trackingphotoconvertible polymer capsulestwo-photon microscopy

Identifiers

PMID39471872
PMCPMC11521627

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.