Evidence map›Paper›PMID 31056478›Full record

ArticleStem cell reports2019

WNT/NOTCH Pathway Is Essential for the Maintenance and Expansion of Human MGE Progenitors.

Lin Ma, Yiran Wang, Yi Hui, Yanhua Du, Zhenyu Chen, Hexi Feng, Shuwei Zhang, Nan Li, Jianren Song, Yujiang Fang and 7 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

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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

17 authors at 3 institutions in 1 country.

Lin MaBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Yiran WangBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Yi HuiBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Yanhua DuBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Zhenyu ChenBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Hexi FengBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Shuwei ZhangBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Nan LiBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Jianren SongBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Reconstruction and Regeneration of Spine and Spinal Cord Injury, Ministry of Education, Shanghai 200065, China.
Yujiang FangBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Xiangjie XuBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Lei ShiBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Bowen ZhangBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Jiayi ChengBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Shanshan ZhouBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Ling LiuBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Reconstruction and Regeneration of Spine and Spinal Cord Injury, Ministry of Education, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China.
Xiaoqing ZhangBrain and Spinal Cord Innovative Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China; Key Laboratory of Reconstruction and Regeneration of Spine and Spinal Cord Injury, Ministry of Education, Shanghai 200065, China; Key Laboratory of Neuroregeneration of Shanghai Universities, Tongji University School of Medicine, 1239 Siping Road, Room 508, Shanghai 200092, China; Tsingtao Advanced Research Institute, Tongji University, Shanghai 200092, China; Shanghai Institute of Stem Cell Research and Clinical Translation, Shanghai 200120, China; Translational Medical Center for Stem Cell Therapy, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China. Electronic address: xqzhang@tongji.edu.cn.
Tongji University · CNTongji Hospital · CNShanghai East Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medial ganglionic eminence (MGE)-like cells yielded from human pluripotent stem cells (hPSCs) hold great potentials for cell therapies of related neurological disorders. However, cues that orchestrate the maintenance versus differentiation of human MGE progenitors, and ways for large-scale expansion of these cells have not been investigated. Here, we report that WNT/CTNNB1 signaling plays an essential role in maintaining MGE-like cells derived from hPSCs. Ablation of CTNNB1 in MGE cells led to precocious cell-cycle exit and advanced neuronal differentiation. Activation of WNT signaling through genetic or chemical approach was sufficient to maintain MGE cells in an expandable manner with authentic neuronal differentiation potencies through activation of endogenous NOTCH signaling. Our findings reveal that WNT/NOTCH signaling cascade is a key player in governing the maintenance versus terminal differentiation of MGE progenitors in humans. Large-scale expansion of functional MGE progenitors for cell therapies can therefore be achieved by modifying WNT/NOTCH pathway.

Indexed as

beta CateninCell CycleCell DifferentiationCell LineCell ProliferationGABAergic NeuronsGene Expression ProfilingGene Regulatory NetworksHumansInterneuronsMedian EminencePluripotent Stem CellsReceptors, NotchWnt Signaling Pathwaybeta CateninCTNNB1 protein, humanReceptors, Notchcell therapyhuman pluripotent stem cellsmaintenancemedial ganglionic eminenceneural progenitorneuronal differentiationNOTCHWNT/CTNNB1

Identifiers

PMID31056478
PMCPMC6524734
OpenAlexW2942992252

What OpenQuestion 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 OpenQuestion graph.