Evidence map›Paper›PMID 42203905›Full record

ArticleCommunications biology2026

Molecular signatures and lineage diversification of neurogenic and gliogenic radial glia in the gyrencephalic ferret cortex.

Jialin Li, Feihong Yang, Weiwei Li, Tongye Fu, Zhenmeiyu Li, Zizhuo Sha, Wenhui Zheng, Chuannan Yang, Jingzhe Yu, Danyu Han and 12 more

Abstract read
In one paragraph

Article in Communications biology, 2026. 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

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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Jialin Li *Department of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0009-0006-7321-030X
Feihong Yang *Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0009-0001-8727-3997
Weiwei Li *Institute of Pediatrics, National Children's Medical Center, Children's Hospital of Fudan University, Shanghai, China.
Tongye FuDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Zhenmeiyu LiDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Zizhuo ShaDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Wenhui ZhengDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Chuannan YangDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Jingzhe YuDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Danyu HanDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Xin JiangDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Yan YouDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Xiaosu LiDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Tong MaDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.
Miao HeDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0000-0003-0731-6801
Zhejun XuDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0000-0002-1933-6300
Xiaolei SongCenter for Clinical and Translational Medicine, Shanghai University of Medicine and Health Sciences, Shanghai, China.
Bin ChenDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, CA, USA.ORCID 0000-0003-1962-3593
Jing DingDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China. ding.jing@zs-hospital.sh.cn.ORCID 0000-0001-5135-4210
Xin WangDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China. wang.xin@zs-hospital.sh.cn.ORCID 0000-0002-6813-2371
Zhuangzhi ZhangDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China. zz_zhang@fudan.edu.cn.ORCID 0000-0002-9860-6689
Zhengang YangDepartment of Neurology, State Key Laboratory of Brain Function and Disorders, Ministry of Education Frontiers Center for Brain Science, Institutes of Brain Science, Zhongshan Hospital, Fudan University, Shanghai, China. yangz@fudan.edu.cn.ORCID 0000-0003-2447-6540

Funding

Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) R01MH094589Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) R01NS089777Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) STI2030-2021ZD0202300National Natural Science Foundation of China (National Science Foundation of China) 32070971National Natural Science Foundation of China (National Science Foundation of China) 32200792National Science Foundation of China | National Natural Science Foundation of China-Yunnan Joint Fund (NSFC-Yunnan Joint Fund) 32200776
6 · The paper itself

Abstract

Human exceptional cognition stems from evolutionarily derived cortical adaptations that drive expansive neurogenesis. In this study, we employ the gyrencephalic ferret model to systematically characterize the molecular profiles and lineage dynamics of cortical radial glia (RGs). By applying scRNA-Seq to ferret and human cortices, we identify conserved regulatory programs underlying cortical neurogenesis and gliogenesis. We show that, similar to their human counterparts, ferret cortical outer radial glia (oRGs), exhibit enhanced ERK and PKA signaling. ERK and PKA act in a mutually reinforcing manner to boost oRG self-renewal and neurogenesis, while inhibiting gliogenesis and prolonging the neurogenic period. Furthermore, we identify regional specialization within cortical gliogenic RGs: YAP/TAZ activation drives ventricular zone truncated radial glia (tRGs) toward ependymal glial fate in medial cortex, whereas SHH signaling instructs tRGs within the ventrolateral-to-dorsal cortical axis to generate tripotential intermediate progenitor cells, which serve as a shared source of astrocytes, oligodendrocytes, and cortically-derived olfactory bulb interneurons. Our findings support a model in which cortical neurogenesis, gliogenesis, and evolutionary expansion are co-regulated through an integrated signaling network orchestrated by ERK, PKA, YAP/TAZ, and SHH. This network relies on a precisely balanced interplay of mutual inhibition among these pathways to ensure proper developmental outcomes.

Indexed as

Cell LineageCerebral CortexEpendymoglial CellsFerretsNeurogenesisNeurogliaAnimalsCell DifferentiationHumansSignal Transduction

Identifiers

PMID42203905
PMCPMC13247174

What OpenQuestion holds

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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.