Evidence map›Paper›PMID 40495808›Full record

ArticleOpen biology2025

Unravelling axonal transcriptional landscapes: insights from induced pluripotent stem cell-derived cortical neurons and implications for motor neuron degeneration.

Jishu Xu, Michaela Hörner, Maike Nagel, Perwin Perhat, Milena Korneck, Marvin Noß, Stefan Hauser, Ludger Schoels, Jakob Admard, Nicolas Casadei and 1 more

Abstract read
In one paragraph

Article in Open biology, 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. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Jishu Xu *Eberhard Karls University Tübingen Hertie Institute for Clinical Brain Research, Tübingen, Baden-Württemberg, Germany.
Michaela Hörner *Division of Neurodegenerative Diseases and Movement Disorders, Department of Neurology, Heidelberg University Hospital, Heidelberg, Baden-Württemberg, Germany.ORCID 0000-0001-5485-4990
Maike NagelEberhard Karls University Tübingen Hertie Institute for Clinical Brain Research, Tübingen, Baden-Württemberg, Germany.
Perwin PerhatDivision of Neurodegenerative Diseases and Movement Disorders, Department of Neurology, Heidelberg University Hospital, Heidelberg, Baden-Württemberg, Germany.
Milena KorneckEberhard Karls University Tübingen Hertie Institute for Clinical Brain Research, Tübingen, Baden-Württemberg, Germany.
Marvin NoßEberhard Karls University Tübingen Hertie Institute for Clinical Brain Research, Tübingen, Baden-Württemberg, Germany.
Stefan HauserEberhard Karls University Tübingen Hertie Institute for Clinical Brain Research, Tübingen, Baden-Württemberg, Germany.
Ludger SchoelsEberhard Karls University Tübingen Hertie Institute for Clinical Brain Research, Tübingen, Baden-Württemberg, Germany.
Jakob AdmardInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Baden-Württemberg, Germany.
Nicolas CasadeiInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Baden-Württemberg, Germany.
Rebecca SchueleEberhard Karls University Tübingen Hertie Institute for Clinical Brain Research, Tübingen, Baden-Württemberg, Germany.ORCID 0000-0002-7781-2766

Funding

Bundesministerium für Bildung und ForschungDeutsche ForschungsgemeinschaftElse Kröner-Fresenius-StiftungEuropean Health and Digital Executive Agency (HADEA) through funding for the European Rare Disease Research Alliance (ERDERA)European Reference Network for Rare Neurological DiseasesNINDS NIH HHS
6 · The paper itself

Abstract

Neuronal function and pathology are deeply influenced by the distinct molecular profiles of the axon and soma. Traditional studies have often overlooked these differences due to the technical challenges of compartment-specific analysis. In this study, we employ a robust RNA-sequencing approach, using microfluidic devices, to generate high-quality axonal transcriptomes from induced pluripotent stem cells-derived cortical neurons (CNs). We achieve high specificity of axonal fractions, ensuring sample purity without contamination. Comparative analysis revealed a unique and specific transcriptional landscape in axonal compartments, characterized by diverse transcript types, including protein-coding mRNAs, RNAs encoding ribosomal proteins, mitochondrial-encoded RNAs and long non-coding RNAs. Previous works have reported the existence of transcription factors (TFs) in the axon. Here, we detect a set of TFs specific to the axon and indicative of their active participation in transcriptional regulation. To investigate transcripts and pathways essential for central motor neuron (MN) degeneration and maintenance we analysed kinesin family member 1C (

Indexed as

AxonsInduced Pluripotent Stem CellsMotor NeuronsNerve DegenerationTranscriptomeAnimalsGene Expression ProfilingHumansKinesinsMiceTranscription FactorsKinesinsTranscription Factorsaxonal transcriptomicsaxonal transportiPSC-derived neuronskinesinneuronstranscription factors

Identifiers

PMID40495808
PMCPMC12152748

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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.