Evidence map›Paper›PMID 37287081›Full record

ArticleStem cell research & therapy2023

TRPA1 promotes the maturation of embryonic stem cell-derived cardiomyocytes by regulating mitochondrial biogenesis and dynamics.

Qianqian Ding, Xianji Liu, Yanxiang Qi, Xiaoqiang Yao, Suk Ying Tsang

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Transient receptor potential channels inChannels (Austin, Tex.) · 2026
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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

5 authors at 1 institution in 2 countries.

Qianqian DingSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Xianji LiuSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Yanxiang QiSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Xiaoqiang YaoSchool of Biomedical Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Suk Ying TsangSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China. fayetsang@cuhk.edu.hk.ORCID 0000-0002-9992-5454
Chinese University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiomyocytes derived from pluripotent stem cells (PSC-CMs) have been widely accepted as a promising cell source for cardiac drug screening and heart regeneration therapies. However, unlike adult cardiomyocytes, the underdeveloped structure, the immature electrophysiological properties and metabolic phenotype of PSC-CMs limit their application. This project aimed to study the role of the transient receptor potential ankyrin 1 (TRPA1) channel in regulating the maturation of embryonic stem cell-derived cardiomyocytes (ESC-CMs).

methodsThe activity and expression of TRPA1 in ESC-CMs were modulated by pharmacological or molecular approaches. Knockdown or overexpression of genes was done by infection of cells with adenoviral vectors carrying the gene of interest as a gene delivery tool. Immunostaining followed by confocal microscopy was used to reveal cellular structure such as sarcomere. Staining of mitochondria was performed by MitoTracker staining followed by confocal microscopy. Calcium imaging was performed by fluo-4 staining followed by confocal microscopy. Electrophysiological measurement was performed by whole-cell patch clamping. Gene expression was measured at mRNA level by qPCR and at protein level by Western blot. Oxygen consumption rates were measured by a Seahorse Analyzer.

resultsTRPA1 was found to positively regulate the maturation of CMs. TRPA1 knockdown caused nascent cell structure, impaired Ca

conclusionsTaken together, our study reveals the novel function of TRPA1 in promoting the maturation of CMs. As multiple stimuli have been known to activate TRPA1, and TRPA1-specific activators are also available, this study provides a novel and straightforward strategy for improving the maturation of PSC-CMs by activating TRPA1. Since a major limitation for the successful application of PSC-CMs for research and medicine lies in their immature phenotypes, the present study takes a big step closer to the practical use of PSC-CMs.

Indexed as

Myocytes, CardiacOrganelle BiogenesisCalciumCell DifferentiationEmbryonic Stem CellsEnzyme Inhibitorsp38 Mitogen-Activated Protein KinasesCalciumEnzyme Inhibitorsp38 Mitogen-Activated Protein KinasesCardiomyocyte maturationEmbryonic stem cell-derived cardiomyocytesMitochondriaPeroxisome proliferator-activated receptor gamma coactivator-1αTransient receptor potential ankyrin 1 channel

Identifiers

PMID37287081
PMCPMC10249273
OpenAlexW4379742952

What OpenQuestion holds

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LicenceCC BY
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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.