Evidence map›Paper›PMID 39825140›Full record

ArticleNature neuroscience2025

Propagation of neuronal micronuclei regulates microglial characteristics.

Sarasa Yano, Natsu Asami, Yusuke Kishi, Ikuko Takeda, Hikari Kubotani, Yuki Hattori, Ayako Kitazawa, Kanehiro Hayashi, Ken-Ichiro Kubo, Mai Saeki and 14 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Expanding roles of cGAS-STING signaling in neuroinflammation.The Journal of clinical investigation · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
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  10. Review
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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

24 authors.

Sarasa YanoGraduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Japan.
Natsu AsamiGraduate School of Science and Technology, University of Tsukuba, Tsukuba, Japan.
Yusuke KishiInstitute for Quantitative Biosciences, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2846-5400
Ikuko TakedaDepartment of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0003-4951-9359
Hikari KubotaniGraduate School of Science and Technology, University of Tsukuba, Tsukuba, Japan.
Yuki HattoriDepartment of Anatomy and Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0001-6576-0121
Ayako KitazawaDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.
Kanehiro HayashiDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.
Ken-Ichiro KuboDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.ORCID http://orcid.org/0000-0003-4023-5069
Mai SaekiInstitute for Quantitative Biosciences, The University of Tokyo, Tokyo, Japan.
Chihiro MaedaGraduate School of Science and Technology, University of Tsukuba, Tsukuba, Japan.
Chihiro HirakiGraduate School of Science and Technology, University of Tsukuba, Tsukuba, Japan.
Rin-Ichiro TeruyaGraduate School of Science and Technology, University of Tsukuba, Tsukuba, Japan.
Takumi TaketomiSchool of Integrative and Global Majors, University of Tsukuba, Tsukuba, Japan.ORCID http://orcid.org/0000-0003-1275-3563
Kaito AkiyamaCollege of Biological Sciences, School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Japan.
Tomomi Okajima-TakahashiGraduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Japan.
Ban SatoInstitute of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Japan.
Hiroaki WakeDepartment of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0002-8543-4590
Yukiko GotohGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0001-9367-6648
Kazunori NakajimaDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.ORCID http://orcid.org/0000-0003-1864-9425
Takeshi IchinoheDepartment of Infectious Disease Control, International Research Center for Infectious Diseases, Institute of Medical Science, The University of Tokyo Minato-ku, Tokyo, Japan.
Takeshi NagataSchool of Integrative and Global Majors, University of Tsukuba, Tsukuba, Japan.
Tomoki ChibaSchool of Integrative and Global Majors, University of Tsukuba, Tsukuba, Japan.
Fuminori TsurutaSchool of Integrative and Global Majors, University of Tsukuba, Tsukuba, Japan. tsuruta.fuminori.fn@u.tsukuba.ac.jp.ORCID http://orcid.org/0000-0002-3471-7654

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 16KK0158MEXT | Japan Society for the Promotion of Science (JSPS) 19J20619MEXT | Japan Society for the Promotion of Science (JSPS) 20K05951MEXT | Japan Society for the Promotion of Science (JSPS) 23H04214MEXT | Japan Society for the Promotion of Science (JSPS) 23KJ0285MEXT | Japan Society for the Promotion of Science (JSPS) 24K02020MEXT | Japan Society for the Promotion of Science (JSPS) JP20H05688MEXT | Japan Society for the Promotion of Science (JSPS) JP22K19365
6 · The paper itself

Abstract

Microglia-resident immune cells in the central nervous system-undergo morphological and functional changes in response to signals from the local environment and mature into various homeostatic states. However, niche signals underlying microglial differentiation and maturation remain unknown. Here, we show that neuronal micronuclei (MN) transfer to microglia, which is followed by changing microglial characteristics during the postnatal period. Neurons passing through a dense region of the developing neocortex give rise to MN and release them into the extracellular space, before being incorporated into microglia and inducing morphological changes. Two-photon imaging analyses have revealed that microglia incorporating MN tend to slowly retract their processes. Loss of the cGAS gene alleviates effects on micronucleus-dependent morphological changes. Neuronal MN-harboring microglia also exhibit unique transcriptome signatures. These results demonstrate that neuronal MN serve as niche signals that transform microglia, and provide a potential mechanism for regulation of microglial characteristics in the early postnatal neocortex.

Indexed as

MicrogliaNeocortexNeuronsAnimalsAnimals, NewbornMiceMice, Inbred C57BLMice, Transgenic

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.