Evidence map›Paper›PMID 39380099›Full record

ReviewStem cell research & therapy2024

Maturation of pluripotent stem cell-derived cardiomyocytes: limitations and challenges from metabolic aspects.

Xi Jiang, Xin Lian, Kun Wei, Jie Zhang, Kaihua Yu, Haoming Li, Haichun Ma, Yin Cai, Lei Pang

Abstract readReview
In one paragraph

Review in Stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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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

9 authors.

Xi JiangHealth management center, the First Hospital of Jilin University, Changchun, China.
Xin LianDepartment of Urology, the First Hospital of Jilin University, Changchun, China.
Kun WeiDepartment of Rehabilitation, The Second Affiliated Hospital, Shandong University of Traditional Chinese Medicine, Shandong, China.
Jie ZhangDepartment of Anesthesiology, the First Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Kaihua YuDepartment of Anesthesiology, the First Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Haoming LiDepartment of Anesthesiology, the First Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Haichun MaDepartment of Anesthesiology, the First Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China.
Yin CaiDepartment of Health Technology and Informatics, the Hong Kong Polytechnic University, Hong Kong, China.
Lei PangDepartment of Anesthesiology, the First Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, China. panglei@jlu.edu.cn.ORCID 0000-0002-2285-2728

Funding

National Natural Science Foundation 82102306Natural Science Foundation of Jilin Province YDZJ202401171ZYTSNatural Science Foundation of Jilin Province YDZJ202401412ZYTSShenzhen Science and Technology Program JCYJ20220531090814032the Natural Science Foundation of Jilin Province YDZJ202401235ZYTS
6 · The paper itself

Abstract

Acute coronary syndromes, such as myocardial infarction (MI), lack effective therapies beyond heart transplantation, which is often hindered by donor scarcity and postoperative complications. Human induced pluripotent stem cells (hiPSCs) offer the possibility of myocardial regeneration by differentiating into cardiomyocytes. However, hiPSC-derived cardiomyocytes (hiPSC-cardiomyocytes) exhibit fetal-like calcium flux and energy metabolism, which inhibits their engraftment. Several strategies have been explored to improve the therapeutic efficacy of hiPSC-cardiomyocytes, such as selectively enhancing energy substrate utilization and improving the transplantation environment. In this review, we have discussed the impact of altered mitochondrial biogenesis and metabolic switching on the maturation of hiPSC-cardiomyocytes. Additionally, we have discussed the limitations inherent in current methodologies for assessing metabolism in hiPSC-cardiomyocytes, and the challenges in achieving sufficient metabolic flexibility akin to that in the healthy adult heart.

Indexed as

Induced Pluripotent Stem CellsMitochondria, HeartMyocardial InfarctionMyocytes, CardiacCell Culture TechniquesHumansRegenerative MedicineAcute coronary syndromesEnergy metabolismInduced pluripotent stem cellsiPSC-cardiomyocytesMaturationMyocardial infarction

Identifiers

PMID39380099
PMCPMC11462682

What OpenQuestion holds

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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.