Evidence map›Paper›PMID 40542444›Full record

ArticleStem cell research & therapy2025

Human induced neural progenitor cells generated from three-dimensional aggregate-based culture significantly improve post-stroke recovery in tMCAO mice.

Zeqin Fu, Yue Hu, Yuxia Wang, Zhijie Liu, Mengyuan Li, Yanqiu Guo, Zhiwei Hu, Xingqiang Lai, Junyuan Hu, Yan Liao and 1 more

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Review
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

11 authors.

Zeqin Fu *Shenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Yue Hu *Shenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Yuxia WangShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Zhijie LiuShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Mengyuan LiShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Yanqiu GuoShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Zhiwei HuShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Xingqiang LaiShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Junyuan HuShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China.
Yan LiaoShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China. liaoyan@beike.cc.
Cheguo CaiShenzhen Beike Biotechnology Co., Ltd, Shenzhen, 518054, China. cheguo_cai@ucas.ac.cn.ORCID http://orcid.org/0000-0002-3712-1696

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2024A1515030277Shenzhen Science and Technology Program JCYJ20210324115011030Shenzhen Science and Technology Program JCYJ20240813162659008Shenzhen Science and Technology Program KJZD20230923114504008
6 · The paper itself

Abstract

backgroundDespite the high prevalence of cerebral ischemic stroke, effective clinical treatments remain limited. With the development of regenerative medicine, induced neural progenitor cells (iNPCs) demonstrate ideal potential and good availability for autologous transplantation therapy. However, current differentiation protocols for iNPCs still have room for improvement in terms of purity, reproducibility, scalability and differentiation potential.

methodsWe aimed to develop a scalable, stable, and efficient 3D aggregate-based method for iNPC production in suspension culture, avoiding detrimental cell dissociation and replating processes. We evaluated the therapeutic potential of iNPCs in the chronic phase of a transient middle cerebral artery occlusion (tMCAO) mouse model and explored iNPC subpopulations via single-cell RNA sequencing to elucidate their pleiotropic therapeutic potentials.

resultsiNPCs generated from three iPSC lines displayed high NPC marker expression and an average 176-fold cell expansion over the 12-day culture period. These iNPCs could spontaneously differentiate into both neurons and glial cells in vitro. In the tMCAO model, transplanted iNPCs remodeled the microenvironment by alleviating neuroinflammation, inhibiting chronic microgliosis and astrogliosis, promoting M2 polarization of microglia, and preserving astrocytic morphology in the ischemic penumbra. Mechanistically, iNPCs can be divided into four subpopulations, with neuroepithelia being the most abundant and capable of rapidly replenishing damaged cells and mitigating microenvironmental deterioration.

conclusionsWe developed a simple and efficient 3D aggregate-based method for iNPC differentiation. These iNPCs showed excellent potential for post-stroke recovery and represent a valuable tool for clinical translation.

Indexed as

Induced Pluripotent Stem CellsInfarction, Middle Cerebral ArteryNeural Stem CellsStrokeAnimalsCell DifferentiationDisease Models, AnimalHumansMaleMiceMice, Inbred C57BL3D aggregatesChronic ischemic strokeInduced neural progenitor cellsPost-stroke recoveryStem cell transplantation

Identifiers

PMID40542444
PMCPMC12181839

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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.