Evidence map›Paper›PMID 41290634›Full record

ArticleNature communications2025

Single rosette-based generation of uniform cortical assembloids recapitulating cellular interactions between neurons and glial cells.

Eunjee Kim, Yunhee Kim, Soojung Hong, Inha Kim, Juhee Lee, Jong-Yeon Yoo, Jihyun Kim, Kwangmin Yoo, Hojin Lee, Joung-Hun Kim and 2 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

12 authors.

Eunjee Kim *Institute of Molecular Biology and Genetics, Seoul National University, Seoul, Republic of Korea.
Yunhee Kim *Institute of Molecular Biology and Genetics, Seoul National University, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0001-5379-7744
Soojung HongInstitute of Molecular Biology and Genetics, Seoul National University, Seoul, Republic of Korea.
Inha KimInstitute of Molecular Biology and Genetics, Seoul National University, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0007-3263-4541
Juhee LeeInstitute of Molecular Biology and Genetics, Seoul National University, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0006-5607-6532
Jong-Yeon YooDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk, Republic of Korea.
Jihyun KimDepartment of Biomedical Sciences, Korea University College of Medicine, Seoul, Republic of Korea.
Kwangmin YooDepartment of Biomedical Sciences, Korea University College of Medicine, Seoul, Republic of Korea.
Hojin LeeDepartment of Biomedical Sciences, Korea University College of Medicine, Seoul, Republic of Korea.
Joung-Hun KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk, Republic of Korea.ORCID http://orcid.org/0000-0001-6716-2037
Jungmin ChoiDepartment of Biomedical Sciences, Korea University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-8614-0973
Kunyoo ShinInstitute of Molecular Biology and Genetics, Seoul National University, Seoul, Republic of Korea. kunyoos@snu.ac.kr.ORCID http://orcid.org/0000-0002-1519-9839

Funding

National Research Foundation of Korea (NRF) RS-2022-NR072198National Research Foundation of Korea (NRF) RS-2023-00223277National Research Foundation of Korea (NRF) RS-2024-00466703
6 · The paper itself

Abstract

Despite recent advances, current brain organoid technologies face ongoing challenges in managing heterogeneity and representing the diverse structure and cell types of the human brain. Here, we develop a module-based cellular reconstitution technology to sequentially build uniform cortical assembloids with mature cortical structures and functional connectivity. The uniformity and maturity of the cortical assembloids are achieved by creating single-rosette-based organoids at the early stage, whose sizes were big and consistent with the treatment of Wnt and Hedgehog agonists, followed by spatial reconstitution with the Reelin-expressing neuronal layer and non-neuronal glial cells. The resulting single-rosette-based cortical assembloids are highly uniform and reproducible without significant batch effects, solving major heterogeneity issues caused by difficulties in controlling the number and size of rosettes in conventional multi-rosette organoids. Furthermore, these cortical assembloids structurally and functionally recapitulate the physiology of the human brain, including the six-layered cortical structure, functional connectivity, and dynamic cellular interplay between neurons and glial cells. Our study thus provides an innovative preclinical model to study a range of neurological disorders, understanding the pathogenesis of which requires an organoid system capable of representing the dynamic cellular interactions and the maturity of the human brain.

Indexed as

Cell CommunicationCerebral CortexNeurogliaNeuronsOrganoidsAnimalsCell Adhesion Molecules, NeuronalHedgehog ProteinsHumansMiceNerve Tissue ProteinsReelin ProteinSerine EndopeptidasesCell Adhesion Molecules, NeuronalHedgehog ProteinsNerve Tissue ProteinsReelin ProteinRELN protein, humanSerine Endopeptidases

Identifiers

PMID41290634
PMCPMC12728168

What OpenQuestion holds

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LicenceCC BY
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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.