Evidence map›Paper›PMID 39515335›Full record

ArticleCell reports methods2024

Generation of self-renewing neuromesodermal progenitors with neuronal and skeletal muscle bipotential from human embryonic stem cells.

Pingxin Sun, Yuan Yuan, Zhuman Lv, Xinlu Yu, Haoxin Ma, Shulong Liang, Jiqianzhu Zhang, Jiangbo Zhu, Junyu Lu, Chunyan Wang and 4 more

Abstract read
In one paragraph

Article in Cell reports methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

14 authors.

Pingxin SunDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China.
Yuan YuanDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China.
Zhuman LvDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China.
Xinlu YuDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China.
Haoxin MaDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China.
Shulong LiangDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China.
Jiqianzhu ZhangDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China; Department of Health Toxicology, Naval Medical University, 200433 Shanghai, China.
Jiangbo ZhuDepartment of Health Toxicology, Naval Medical University, 200433 Shanghai, China.
Junyu LuDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China.
Chunyan WangDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China.
Le HuanDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China. Electronic address: dr.huan@hotmail.com.
Caixia JinDepartment of Regenerative Medicine, College of Medicine, Tongji University, 200433 Shanghai, China. Electronic address: jincx@tongji.edu.cn.
Chao WangDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China. Electronic address: wangchaosmmu@126.com.
Wenlin LiDepartment of Cell Biology, Naval Medical University, 200433 Shanghai, China; Shanghai Key Laboratory of Cell Engineering, Naval Medical University, 200433 Shanghai, China. Electronic address: liwenlin@smmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progress has been made in generating spinal cord and trunk derivatives from neuromesodermal progenitors (NMPs). However, maintaining the self-renewal of NMPs in vitro remains a challenge. In this study, we developed a cocktail of small molecules and growth factors that induces human embryonic stem cells to produce self-renewing NMPs (srNMPs) under chemically defined conditions. These srNMPs maintain the state of neuromesodermal progenitors in prolonged culture and have the potential to generate mesodermal cells and neurons, even at the single-cell level. Additionally, suspended srNMP aggregates can spontaneously differentiate into all tissue types of early embryonic trunks. Furthermore, transplanted srNMP-derived muscle satellite cells or progenitors of motor neurons were integrated into skeletal muscle or the spinal cord, respectively, and contributed to regeneration in mouse models. In summary, srNMPs hold great promise for applications in developmental biology and as renewable cell sources for cell therapy for trunk and spinal cord injuries.

Indexed as

Cell DifferentiationHuman Embryonic Stem CellsMuscle, SkeletalAnimalsCells, CulturedCell Self RenewalHumansMesodermMiceMotor NeuronsNeural Stem CellsNeuronscell therapyCP: Stem cellhuman embryonic stem cellshuman pluripotent stem cellsneuromesodermal progenitorsself-renewalskeletal muscle injuryspinal cord injury

Identifiers

PMID39515335
PMCPMC11705767

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.