Evidence map›Paper›PMID 40055379›Full record

ArticleNature communications2025

Spatiotemporally resolved transcriptomics reveals the cellular dynamics of human retinal development.

Jinglong Zhang, Jiao Wang, Qiongjie Zhou, Zixin Chen, Junyi Zhuang, Xingzhong Zhao, Ziquan Gan, Yinan Wang, Chunxiu Wang, Robert S Molday and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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  10. Analysis ofInternational journal of molecular sciences · 2025
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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

13 authors.

Jinglong Zhang *Department of Neurology, Zhongshan Hospital and Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China.ORCID http://orcid.org/0000-0001-6795-1423
Jiao Wang *School of Life Sciences, Shanghai University, Shanghai, China.
Qiongjie Zhou *Department of Obstetrics, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Zixin ChenSchool of Life Sciences, Shanghai University, Shanghai, China.
Junyi ZhuangSchool of Life Sciences, Shanghai University, Shanghai, China.
Xingzhong ZhaoDepartment of Neurology, Zhongshan Hospital and Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China.
Ziquan GanDepartment of Neurology, Zhongshan Hospital and Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China.
Yinan WangDepartment of Obstetrics, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Chunxiu WangDepartment of Obstetrics, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Robert S MoldayDepartment of Biochemistry & Molecular Biology, University of British Columbia, Vancouver, BC, Canada.
Yucheng T YangDepartment of Neurology, Zhongshan Hospital and Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China. yangyy@fudan.edu.cn.ORCID http://orcid.org/0000-0002-6873-5279
Xiaotian LiDepartment of Obstetrics, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China. xiaotianli555@163.com.ORCID http://orcid.org/0000-0002-2051-4581
Xing-Ming ZhaoDepartment of Neurology, Zhongshan Hospital and Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China. xmzhao@fudan.edu.cn.ORCID http://orcid.org/0000-0002-4531-3970

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The morphogenesis and cellular interactions in developing retina are incompletely characterized. The full understanding needs a precise mapping of the gene expression with a single-cell spatial resolution. Here, we present a spatial transcriptomic (ST) resource for the developing human retina at six developmental stages. Combining the spatial and single-cell transcriptomic data enables characterization of the cell-type-specific expression profiles at distinct anatomical regions at each developmental stage, highlighting the spatiotemporal dynamics of cellular composition during retinal development. All the ST spots are catalogued into consensus spatial domains, which are further associated to their specific expression signatures and biological functions associated with neuron and eye development. We prioritize a set of critical regulatory genes for the transitions of spatial domains during retinal development. Differentially expressed genes from different spatial domains are associated with distinct retinal diseases, indicating the biological relevance and clinical significance of the spatially defined gene expression. Finally, we reconstruct the spatial cellular communication networks, and highlight critical ligand-receptor interactions during retinal development. Overall, our study reports the spatiotemporal dynamics of gene expression and cellular profiles during retinal development, and provides a rich resource for the future studies on retinogenesis.

Indexed as

RetinaTranscriptomeCell CommunicationGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansSingle-Cell AnalysisSpatio-Temporal Analysis

Identifiers

PMID40055379
PMCPMC11889126

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.