Evidence map›Paper›PMID 38900068›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Injectable biodegradable microcarriers for iPSC expansion and cardiomyocyte differentiation.

Annalisa Bettini, Patrizia Camelliti, Daniel J Stuckey, Richard M Day

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Injectable biodegradable microcarriers for iPSC expansion and cardiomyocyte differentiation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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

4 authors.

Annalisa BettiniCentre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, UK.ORCID 0009-0007-9838-3722
Patrizia CamellitiSchool of Biosciences and Medicine, University of Surrey, Guildford, Surrey, GU2 7XH, UK.ORCID 0000-0002-1346-8089
Daniel J StuckeyCentre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, UK.ORCID 0000-0001-8888-627X
Richard M DayCentre for Precision Healthcare, Division of Medicine, University College London, London, WC1E 6JF, UK.ORCID 0000-0002-3124-2294

Funding

British Heart Foundation FS/15/33/31608British Heart Foundation FS/17/33/32931British Heart Foundation FS/17/70/33482British Heart Foundation FS/SBSRF/21/31020British Heart Foundation PG/22/11172British Heart Foundation Centre of Regenerative Medicine RM/17/1/33377Medical Research Council MR/R014108/1National Institute of Health Research (NIHR) for the UCLH Biomedical Research CentreRoyal Society RSG/R1/180198Wellcome Trust 212937/Z/18/Z
6 · The paper itself

Abstract

Cell therapy is a potential novel treatment for cardiac regeneration and numerous studies have attempted to transplant cells to regenerate the myocardium lost during myocardial infarction. To date, only minimal improvements to cardiac function have been reported. This is likely to be the result of low cell retention and survival following transplantation. This study aimed to improve the delivery and engraftment of viable cells by using an injectable microcarrier that provides an implantable, biodegradable substrate for attachment and growth of cardiomyocytes derived from induced pluripotent stem cells (iPSC). We describe the fabrication and characterisation of Thermally Induced Phase Separation (TIPS) microcarriers and their surface modification to enable iPSC-derived cardiomyocyte attachment in xeno-free conditions is described. The selected formulation resulted in iPSC attachment, expansion, and retention of pluripotent phenotype. Differentiation of iPSC into cardiomyocytes on the microcarriers is investigated in comparison with culture on 2D tissue culture plastic surfaces. Microcarrier culture is shown to support culture of a mature cardiomyocyte phenotype, be compatible with injectable delivery, and reduce anoikis. The findings from this study demonstrate that TIPS microcarriers provide a supporting matrix for culturing iPSC and iPSC-derived cardiomyocytes in vitro and are suitable as an injectable cell-substrate for cardiac regeneration.

Indexed as

Cell DifferentiationInduced Pluripotent Stem CellsMyocytes, CardiacBiocompatible MaterialsCell Culture TechniquesCells, CulturedHumansBiocompatible Materialscardiac regenerationcardiomyocyte maturationinjectable biomaterialsmicrocarriersstem cells

Identifiers

PMID38900068
PMCPMC11348074

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Registered trials

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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.