Evidence map›Paper›PMID 42771501›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

System-level synchronization and subtype-specific modules govern brain-wide serotonin axon innervation.

Annabel M J Adams, Kenneth Lap Kei Wu, Zhongyu Li, Peiqi Li, Hangzhen Pan, Zuqi Huang, Sara Migliarini, Richard Dear, Bo Sun, Zora Chui-Kuen Chan and 6 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Annabel M J Adams *Neurobiology Division, The Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.ORCID 0009-0001-1234-2783
Kenneth Lap Kei Wu *Neurobiology Division, The Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.ORCID 0000-0002-3987-6830
Zhongyu LiNeurobiology Division, The Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.
Peiqi LiDepartment of Intelligent Systems, School of Software Engineering, Xi'an Jiaotong University, Xi'an 710049, China.
Hangzhen PanDepartment of Intelligent Systems, School of Software Engineering, Xi'an Jiaotong University, Xi'an 710049, China.
Zuqi HuangDepartment of Intelligent Systems, School of Software Engineering, Xi'an Jiaotong University, Xi'an 710049, China.
Sara MigliariniDepartment of Biology, Unit of Cell and Developmental Biology, University of Pisa, Pisa 56127, Italy.ORCID 0000-0003-2741-269X
Richard DearDepartment of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom.ORCID 0000-0002-1670-6767
Bo SunHuffington Center on Aging, Baylor College of Medicine, Houston, TX 77030.ORCID 0009-0008-5618-6314
Zora Chui-Kuen ChanNeurobiology Division, The Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.
Jingwen LiangNeurobiology Division, The Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.ORCID 0000-0002-9402-2010
Hongjie LiHuffington Center on Aging, Baylor College of Medicine, Houston, TX 77030.ORCID 0000-0002-7332-7122
Petra E VértesDepartment of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom.ORCID 0000-0002-0992-3210
Massimo PasqualettiDepartment of Biology, Unit of Cell and Developmental Biology, University of Pisa, Pisa 56127, Italy.ORCID 0000-0002-0844-8139
Alina IsakovaBrain Resilience Lab, Knight Initiative for Brain Resilience, Wu Tsai Neuroscience Institute, Stanford University, Stanford, CA 94305.ORCID 0000-0003-1113-6889
Jing RenNeurobiology Division, The Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.ORCID 0000-0002-6665-7457

Funding

EU H2020 MSCA Innovative Training Networks N 953327NARSAD Young Investigator Award 2020 BBRFNext Generation EU National Recovery and Resilience Plan n ECS 00000017The Knight Initiative for Brain Resilience n/aUKRI | Medical Research Council (MRC) MC_UP_1201/22UKRI | Medical Research Council (MRC) PhD studentship
6 · The paper itself

Abstract

The serotonin system modulates nearly all neural circuits across development and adulthood and is a major pharmacological target for mood and anxiety disorders. Forebrain-projecting serotonin neurons are organized into projection-defined subsystems that align with molecular heterogeneity, but how these subsystems assemble during development remains unclear. We combined whole-brain developmental projection maps with single-cell transcriptomics to define the spatiotemporal and molecular logic of postnatal serotonin innervation. Using a deep-learning pipeline, we generated four-dimensional whole-brain maps of postnatal serotonin axon density and uncovered two coupled modes of regulation: region-specific trajectories of axon growth and refinement, and an early-postnatal, brain-wide synchronization of innervation. To link these dynamics to cell-intrinsic programs, we profiled single-cell transcriptomes of forebrain-projecting serotonin neurons from embryonic through postnatal stages and reconstructed developmental trajectories. We found that serotonin neuron heterogeneity was established embryonically and that the subtype taxonomy was largely conserved between mice and humans. Across serotonin subtypes, we observed a coordinated surge in wiring-molecule expression at mouse postnatal day 4 that aligned with the subsequent global innervation wave. Tracing subtypes defined by developmentally conserved markers at birth revealed complementary projection territories and engagement of distinct postnatal wiring modules that matched region-specific terminal maturation. Together, these results show that brain-wide serotonin innervation is built through embryonic subtype specification and two layers of postnatal control: system-level synchronization and subtype-specific terminal development.

Indexed as

AxonsBrainSerotonergic NeuronsSerotoninAnimalsFemaleHumansMiceNeurodevelopmentTranscriptomeSerotonindevelopmentserotonintranscriptomicswhole brain mappingwiring specificity

Identifiers

PMID42771501
PMCPMC13624646

What Socratic holds

Textmetadata
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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.