Evidence map›Paper›PMID 36677111›Full record

ArticleMicromachines2022

Polymer Kernels as Compact Carriers for Suspended Cardiomyocytes.

Mikhail Slotvitsky, Andrey Berezhnoy, Serafima Scherbina, Beatrisa Rimskaya, Valerya Tsvelaya, Victor Balashov, Anton E Efimov, Igor Agapov, Konstantin Agladze

Open access · goldAbstract read
In one paragraph

Article in Micromachines, 2022. 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
0.8field-weighted citation impact, top 32% of its field
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, 8 citations in OpenAlex.

  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

9 authors at 2 institutions in 1 country.

Mikhail SlotvitskyMoscow Institute of Physics and Technology, Institutskiy Lane 9, 141700 Dolgoprudny, Russia.ORCID 0000-0003-2237-4217
Andrey BerezhnoyMoscow Institute of Physics and Technology, Institutskiy Lane 9, 141700 Dolgoprudny, Russia.ORCID 0000-0001-8484-6510
Serafima ScherbinaMoscow Institute of Physics and Technology, Institutskiy Lane 9, 141700 Dolgoprudny, Russia.
Beatrisa RimskayaMoscow Institute of Physics and Technology, Institutskiy Lane 9, 141700 Dolgoprudny, Russia.
Valerya TsvelayaMoscow Institute of Physics and Technology, Institutskiy Lane 9, 141700 Dolgoprudny, Russia.
Victor BalashovMoscow Institute of Physics and Technology, Institutskiy Lane 9, 141700 Dolgoprudny, Russia.
Anton E EfimovAcademician V.I. Shumakov National Medical Research Center of Transplantology and Artificial Organs, Ministry of Health of the Russian Federation, Schukinskaya St., 1, 123182 Moscow, Russia.ORCID 0000-0002-0769-301X
Igor AgapovAcademician V.I. Shumakov National Medical Research Center of Transplantology and Artificial Organs, Ministry of Health of the Russian Federation, Schukinskaya St., 1, 123182 Moscow, Russia.
Konstantin AgladzeMoscow Institute of Physics and Technology, Institutskiy Lane 9, 141700 Dolgoprudny, Russia.ORCID 0000-0002-9258-436X
Moscow Institute of Physics and Technology · RUV.I.Shumakov Federal Research Center of Transplantology and Artificial Organs · RU

Funding

Strategic academic leadership program 'Priority 2030 Agreement 075-02-2021-1316 30.09.2021
6 · The paper itself

Abstract

Induced pluripotent stem cells (iPSCs) constitute a potential source of patient-specific human cardiomyocytes for a cardiac cell replacement therapy via intramyocardial injections, providing a major benefit over other cell sources in terms of immune rejection. However, intramyocardial injection of the cardiomyocytes has substantial challenges related to cell survival and electrophysiological coupling with recipient tissue. Current methods of manipulating cell suspensions do not allow one to control the processes of adhesion of injected cells to the tissue and electrophysiological coupling with surrounding cells. In this article, we documented the possibility of influencing these processes using polymer kernels: biocompatible fiber fragments of subcellular size that can be adsorbed to a cell, thereby creating the minimum necessary adhesion foci to shape the cell and provide support for the organization of the cytoskeleton and the contractile apparatus prior to adhesion to the recipient tissue. Using optical excitation markers, the restoration of the excitability of cardiomyocytes in suspension upon adsorption of polymer kernels was shown. It increased the likelihood of the formation of a stable electrophysiological coupling in vitro. The obtained results may be considered as a proof of concept that the stochastic engraftment process of injected suspension cells can be controlled by smart biomaterials.

Indexed as

cell culturingelectrophysiological couplingelectrospinningiPSC-CMpolymers

Identifiers

PMID36677111
PMCPMC9865253
OpenAlexW4313260277

What Socratic 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 Socratic graph.