Evidence map›Paper›PMID 39763780›Full record

ArticlebioRxiv : the preprint server for biology2024

Genetically Labeled Premyelinating Oligodendrocytes: Bridging Oligodendrogenesis and Neuronal Activity.

Aksheev Bhambri, Phu Thai, Songtao Wei, Han-Gyu Bae, Daniela Barbosa, Tripti Sharma, Ze Yu, Chao Xing, Jun Hee Kim, Guoqiang Yu and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

11 authors.

Aksheev BhambriDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0001-9642-5422
Phu ThaiDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Songtao WeiBradley Department of Electrical and Computer Engineering, Virginia Polytechnic Institute and State University, Arlington, VA 22203, USA.
Han-Gyu BaeKresge Hearing Research Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Daniela BarbosaDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Tripti SharmaChildren's Research Institute Mouse Genome Engineering Core, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Ze YuMcDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Chao XingMcDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-1838-0502
Jun Hee KimKresge Hearing Research Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Guoqiang YuDepartment of Automation, Tsinghua University, Beijing 100084, China.
Lu O SunDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

Funding

Novel Genetically Encoded Indicators for Interrogating Neuron-Astrocyte Communication Across TimescalesU19NS123719 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI TIAN, LIN · 2021 to 2025
$10.7M
Role of Adaptive Myelination in Auditory Brain PlasticityR01DC018797 · NIDCD · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Jun Hee Kim · 2021 to 2026
$2.9M
Molecular and genetic decoding of neuron-glial interactionsDP2MH129988 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI SUN, LU · 2021 to 2024
$2.6M
NIDCD NIH HHS R01 DC018797NIMH NIH HHS DP2 MH129988NINDS NIH HHS U19 NS123719
6 · The paper itself

Abstract

To myelinate axons, oligodendrocyte precursor cells (OPCs) must stop dividing and differentiate into premyelinating oligodendrocytes (preOLs). PreOLs are thought to survey and begin ensheathing nearby axons, and their maturation is often stalled at human demyelinating lesions. Lack of genetic tools to visualize and manipulate preOLs has left this critical differentiation stage woefully understudied. Here, we generated a knock-in mouse line that specifically labels preOLs across the central nervous system. Genetically labeled preOLs exhibit distinct morphology, unique transcriptomic and electrophysiological features, and do not overlap with OPCs. PreOL lineage tracing revealed that subsets of them undergo prolonged maturation and that different brain regions initiate oligodendrogenesis with the spatiotemporal specificity. Lastly, by fate mapping preOLs under sensory deprivation, we find that neuronal activity functions within a narrow time window of preOL maturation to promote their survival and successful integration. Our work provides a new tool to probe this critical cell stage during axon ensheathment, allowing for fine dissection of axon-oligodendrocyte interactions.

Indexed as

CRISPR knock-inmyelinationneuronal activityoligodendrocyte precursor cellPremyelinating oligodendrocytesingle-nuclei RNA sequencingwhole-cell patch clamp recordings

Identifiers

PMID39763780
PMCPMC11703227

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.