Evidence map›Paper›PMID 39318247›Full record

ArticleGlia2025

The role of ATP citrate lyase in myelin formation and maintenance.

Andrew Schneider, Seongsik Won, Eric A Armstrong, Aaron J Cooper, Amulya Suresh, Rachell Rivera, Gregory Barrett-Wilt, John M Denu, Judith A Simcox, John Svaren

Abstract read
In one paragraph

Article in Glia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
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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

10 authors.

Andrew SchneiderWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0002-3111-0216
Seongsik WonWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Eric A ArmstrongWisconsin Institute of Discovery, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Aaron J CooperWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Amulya SureshWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Rachell RiveraWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0009-0001-9733-5549
Gregory Barrett-WiltBiotechnology Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.
John M DenuWisconsin Institute of Discovery, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Judith A SimcoxHoward Hughes Medical Institute, Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.
John SvarenWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID 0000-0003-2963-7921

Funding

WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
Waisman Center Intellectual and Developmental Disabilities Research CenterP50HD105353 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI Qiang Chang · 2021 to 2026
$8.5M
Dynamics and molecular mechanisms linking metabolism and the epigenomeR35GM149279 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI JOHN M DENU · 2023 to 2026
$2.8M
Schwann Cell Reprogramming after Nerve InjuryR01NS130566 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI Rajeshwar B Awatramani, John P Svaren · 2023 to 2026
$2.0M
Short-Term Research Training of Veterinary Students in WisconsinT35OD011078 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI BJORLING, DALE EDMOND, JORGENSEN, JOAN S · 2012 to 2025
$1.0M
NICHD NIH HHS P50 HD105353NIDDK NIH HHS P30 DK020579NIGMS NIH HHS R35 GM149279NIH HHS T35 OD011078NINDS NIH HHS R01 NS130566
6 · The paper itself

Abstract

Formation of myelin by Schwann cells is tightly coupled to peripheral nervous system development and is important for neuronal function and long-term maintenance. Perturbation of myelin causes a number of specific disorders that are among the most prevalent diseases affecting the nervous system. Schwann cells synthesize myelin lipids de novo rather than relying on uptake of circulating lipids, yet one unresolved matter is how acetyl CoA, a central metabolite in lipid formation is generated during myelin formation and maintenance. Recent studies have shown that glucose-derived acetyl CoA itself is not required for myelination. However, the importance of mitochondrially-derived acetyl CoA has never been tested for myelination in vivo. Therefore, we have developed a Schwann cell-specific knockout of the ATP citrate lyase (Acly) gene to determine the importance of mitochondrial metabolism to supply acetyl CoA in nerve development. Intriguingly, the ACLY pathway is important for myelin maintenance rather than myelin formation. In addition, ACLY is required to maintain expression of a myelin-associated gene program and to inhibit activation of the latent Schwann cell injury program.

Indexed as

ATP Citrate (pro-S)-LyaseMyelin SheathSchwann CellsAcetyl Coenzyme AAnimalsMiceMice, KnockoutMitochondriaAcetyl Coenzyme AATP Citrate (pro-S)-Lyaseacetyl CoAlipidlipidomicmyelinSchwann

Identifiers

PMID39318247
PMCPMC11660526

What OpenQuestion holds

Textmetadata
LicenceTDM
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.