Evidence map›Paper›PMID 40304297›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

MEA-seqX: High-Resolution Profiling of Large-Scale Electrophysiological and Transcriptional Network Dynamics.

Brett Addison Emery, Xin Hu, Diana Klütsch, Shahrukh Khanzada, Ludvig Larsson, Ionut Dumitru, Jonas Frisén, Joakim Lundeberg, Gerd Kempermann, Hayder Amin

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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. Article
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

10 authors.

Brett Addison EmeryGerman Center for Neurodegenerative Diseases (DZNE), Group "Biohybrid Neuroelectronics", Tatzberg 41, 01307, Dresden, Germany.
Xin HuGerman Center for Neurodegenerative Diseases (DZNE), Group "Biohybrid Neuroelectronics", Tatzberg 41, 01307, Dresden, Germany.
Diana KlütschGerman Center for Neurodegenerative Diseases (DZNE), Group "Biohybrid Neuroelectronics", Tatzberg 41, 01307, Dresden, Germany.
Shahrukh KhanzadaGerman Center for Neurodegenerative Diseases (DZNE), Group "Biohybrid Neuroelectronics", Tatzberg 41, 01307, Dresden, Germany.
Ludvig LarssonScience for Life Laboratory, Department of Gene Technology, KTH Royal Institute of Technology, Tomtebodavägen 23, 17165, Stockholm, Sweden.
Ionut DumitruDepartment of Cell and Molecular Biology, Karolinska Institute, Berzelius väg 35, 17165, Stockholm, Sweden.
Jonas FrisénDepartment of Cell and Molecular Biology, Karolinska Institute, Berzelius väg 35, 17165, Stockholm, Sweden.
Joakim LundebergScience for Life Laboratory, Department of Gene Technology, KTH Royal Institute of Technology, Tomtebodavägen 23, 17165, Stockholm, Sweden.
Gerd KempermannGerman Center for Neurodegenerative Diseases (DZNE), Group "Adult Neurogenesis", Tatzberg 41, 01307, Dresden, Germany.
Hayder AminGerman Center for Neurodegenerative Diseases (DZNE), Group "Biohybrid Neuroelectronics", Tatzberg 41, 01307, Dresden, Germany.ORCID https://orcid.org/0000-0002-6515-2991

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Concepts of brain function imply congruence and mutual causal influence between molecular events and neuronal activity. Decoding entangled information from concurrent molecular and electrophysiological network events demands innovative methodology bridging scales and modalities. The MEA-seqX platform, integrating high-density microelectrode arrays, spatial transcriptomics, optical imaging, and advanced computational strategies, enables the simultaneous recording and analysis of molecular and electrical network activities at mesoscale spatial resolution. Applied to a mouse hippocampal model of experience-dependent plasticity, MEA-seqX unveils massively enhanced nested dynamics between transcription and function. Graph-theoretic analysis reveals an increase in densely connected bimodal hubs, marking the first observation of coordinated hippocampal circuitry dynamics at molecular and functional levels. This platform also identifies different cell types based on their distinct bimodal profiles. Machine-learning algorithms accurately predict network-wide electrophysiological activity features from spatial gene expression, demonstrating a previously inaccessible convergence across modalities, time, and scales.

Indexed as

Electrophysiological PhenomenaGene Regulatory NetworksHippocampusAnimalsGene Expression ProfilingMachine LearningMiceNeuronal PlasticityNeuronsAI machine‐learningconnectomeexperience‐dependent plasticitylarge‐scale neural recordingspredictive modelingspatial transcriptomicsspatiotemporal dynamics

Identifiers

PMID40304297
PMCPMC12120740

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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.