Evidence map›Paper›PMID 38732656›Full record

ArticlePolymers2024

Deep Learning for Cell Migration in Nonwoven Materials and Evaluating Gene Transfer Effects following AAV6-ND4 Transduction.

Ilya I Larin, Rimma O Shatalova, Victor S Laktyushkin, Stanislav A Rybtsov, Evgeniy V Lapshin, Daniil V Shevyrev, Alexander V Karabelsky, Alexander P Moskalets, Dmitry V Klinov, Dimitry A Ivanov

Abstract read
In one paragraph

Article in Polymers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

10 authors.

Ilya I LarinCenter for Translational Medicine, Sirius University of Science and Technology, Krasnodar Territory Sirius, 1 Olympic Ave., Sirius 354340, Russia.ORCID 0000-0002-5005-0749
Rimma O ShatalovaCenter for Translational Medicine, Sirius University of Science and Technology, Krasnodar Territory Sirius, 1 Olympic Ave., Sirius 354340, Russia.
Victor S LaktyushkinResource Center for Cell Technology and Immunology, Sirius University of Science and Technology, Krasnodar Territory Sirius, 1 Olympic Ave., Sirius 354340, Russia.
Stanislav A RybtsovResource Center for Cell Technology and Immunology, Sirius University of Science and Technology, Krasnodar Territory Sirius, 1 Olympic Ave., Sirius 354340, Russia.ORCID 0000-0001-7786-1878
Evgeniy V LapshinCenter for Translational Medicine, Sirius University of Science and Technology, Krasnodar Territory Sirius, 1 Olympic Ave., Sirius 354340, Russia.ORCID 0000-0003-4404-2758
Daniil V ShevyrevResource Center for Cell Technology and Immunology, Sirius University of Science and Technology, Krasnodar Territory Sirius, 1 Olympic Ave., Sirius 354340, Russia.ORCID 0000-0002-7084-081X
Alexander V KarabelskyCenter for Translational Medicine, Sirius University of Science and Technology, Krasnodar Territory Sirius, 1 Olympic Ave., Sirius 354340, Russia.ORCID 0000-0002-6391-5182
Alexander P MoskaletsFederal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical Biological Agency, Moscow 119435, Russia.
Dmitry V KlinovFederal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical Biological Agency, Moscow 119435, Russia.
Dimitry A IvanovCenter for Genetics and Life Sciences, Sirius University of Science and Technology, Krasnodar Territory Sirius, 1 Olympic Ave., Sirius 354340, Russia.ORCID 0000-0002-5905-2652

Funding

Agreement No. 075-10-2021-093 Projects No. GTH-RND-2112 and BMA-RND-2006
6 · The paper itself

Abstract

Studying cell settlement in the three-dimensional structure of synthetic biomaterials over time is of great interest in research and clinical translation for the development of artificial tissues and organs. Tracking cells as physical objects improves our understanding of the processes of migration, homing, and cell division during colonisation of the artificial environment. In this study, the 3D environment had a direct effect on the behaviour of biological objects. Recently, deep learning-based algorithms have shown significant benefits for cell segmentation tasks and, furthermore, for biomaterial design optimisation. We analysed the primary LHON fibroblasts in an artificial 3D environment after adeno-associated virus transduction. Application of these tools to model cell homing in biomaterials and to monitor cell morphology, migration and proliferation indirectly demonstrated restoration of the normal cell phenotype after gene manipulation by AAV transduction. Following the 3Rs principles of reducing the use of living organisms in research, modeling the formation of tissues and organs by reconstructing the behaviour of different cell types on artificial materials facilitates drug testing, the study of inherited and inflammatory diseases, and wound healing. These studies on the composition and algorithms for creating biomaterials to model the formation of cell layers were inspired by the principles of biomimicry.

Indexed as

AAVcell homing and migrationelectrospunfibroblastsmatsneural networktransduction

Identifiers

PMID38732656
PMCPMC11085928

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.