Evidence map›Paper›PMID 39871935›Full record

ArticleLife medicine2022

The long-term survival and functional maturation of human iNPC-derived neurons in the basal forebrain of cynomolgus monkeys.

Su Feng, Ting Zhang, Wei Ke, Yujie Xiao, Zhong Guo, Chunling Lu, Shuntang Li, Zhongxin Guo, Yuanyuan Liu, Guohe Tan and 5 more

Abstract read
In one paragraph

Article in Life medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. The landscape of aging.Science China. Life sciences · 2022
    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

15 authors.

Su FengBioland Laboratory/Guangzhou Laboratory, Guangzhou 510005, China.
Ting ZhangState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, Shanghai 200031, China.
Wei KeDepartment of Neurology, Huashan Hospital, State Key Laboratory of Medical Neurobiology, Institutes for Translational Brain Research, MOE Frontiers Center for Brain Science, Fudan University, Shanghai 200032, China.
Yujie XiaoDepartment of Neurology, Huashan Hospital, State Key Laboratory of Medical Neurobiology, Institutes for Translational Brain Research, MOE Frontiers Center for Brain Science, Fudan University, Shanghai 200032, China.
Zhong GuoWincon TheraCells Biotechnologies Co, LTD, Nanning 530000, China.
Chunling LuWincon TheraCells Biotechnologies Co, LTD, Nanning 530000, China.
Shuntang LiGuangxi Key Laboratory of Regenerative Medicine and Key Laboratory of Longevity and Aging-related Diseases of Chinese Ministry of Education, Collaborative Innovation Centre of Regenerative Medicine and Medical BioResource Development and Application Co-constructed by the Province and Ministry, School of Basic Medical Sciences, Guangxi Medical University, Nanning 530021, China.
Zhongxin GuoGuangxi Key Laboratory of Regenerative Medicine and Key Laboratory of Longevity and Aging-related Diseases of Chinese Ministry of Education, Collaborative Innovation Centre of Regenerative Medicine and Medical BioResource Development and Application Co-constructed by the Province and Ministry, School of Basic Medical Sciences, Guangxi Medical University, Nanning 530021, China.
Yuanyuan LiuGuangxi Key Laboratory of Regenerative Medicine and Key Laboratory of Longevity and Aging-related Diseases of Chinese Ministry of Education, Collaborative Innovation Centre of Regenerative Medicine and Medical BioResource Development and Application Co-constructed by the Province and Ministry, School of Basic Medical Sciences, Guangxi Medical University, Nanning 530021, China.
Guohe TanGuangxi Key Laboratory of Regenerative Medicine and Key Laboratory of Longevity and Aging-related Diseases of Chinese Ministry of Education, Collaborative Innovation Centre of Regenerative Medicine and Medical BioResource Development and Application Co-constructed by the Province and Ministry, School of Basic Medical Sciences, Guangxi Medical University, Nanning 530021, China.
Yingying ChenState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, Shanghai 200031, China.
Feng YueWincon TheraCells Biotechnologies Co, LTD, Nanning 530000, China.
Yousheng ShuDepartment of Neurology, Huashan Hospital, State Key Laboratory of Medical Neurobiology, Institutes for Translational Brain Research, MOE Frontiers Center for Brain Science, Fudan University, Shanghai 200032, China.ORCID https://orcid.org/0000-0002-2834-2876
Chunmei YueState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, Shanghai 200031, China.
Naihe JingBioland Laboratory/Guangzhou Laboratory, Guangzhou 510005, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human induced neural stem/progenitor cells (iNPCs) are a promising source of cells for stem cell-based therapy. The therapeutic potential of human iNPCs has been extensively tested in animal models, including both mouse and monkey models. However, the comprehensive characterization of grafted iNPCs in the brain of non-human primates has been lagged behind. In this study, we transplanted human iNPCs into the basal forebrain of adult cynomolgus monkeys. We found that grafted iNPCs predominantly differentiated into neurons that displayed long-term survival up to 12 months. Additionally, iNPC-derived human neurons gradually matured in term of morphology and subtype differentiation. More excitingly, we observed that human neurons displayed electrophysiological activities resembling those of mature neurons, indicating the acquisition of functional membrane properties. Collectively, this study systematically characterized human iNPCs in the brain of non-human primates, and will provide invaluable clues for developing safe and effective stem cell-based therapies for different brain disorders.

Indexed as

cerebral cell transplantationfunctional maturationhuman induced neural stem/progenitor cellsneuronal differentiationnon-human primates

Identifiers

PMID39871935
PMCPMC11749281

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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.