Evidence map›Paper›PMID 41331335›Full record

ArticleGlia2026

Astrocyte MCT1 Expression Does Not Contribute to the Axonal Degenerative Phenotype Observed With Ubiquitous MCT1 Depletion.

Thomas Philips, Emily G Thompson, Olivia Spead, Balaji G Vijayakumar, Erica R Kent, Sean J Miller, Treasure Nwokeleme, Svetlana Vidensky, Mohamed Hassan Farah, Jeffrey D Rothstein

Abstract read
In one paragraph

Article in Glia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Thomas PhilipsDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Emily G ThompsonDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Olivia SpeadDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Balaji G VijayakumarDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Erica R KentDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Sean J MillerBrain Science Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Treasure NwokelemeDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Svetlana VidenskyDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Mohamed Hassan FarahDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jeffrey D RothsteinDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Funding

Nuclear and Glial Dysfunction in NeurodegenerationR35NS132179 · NINDS · JOHNS HOPKINS UNIVERSITY · PI Jeffrey D Rothstein · 2023 to 2026
$4.9M
ALS AssociationDepartment of DefenseMuscular Dystrophy Association 381190NIH HHSNINDS NIH HHS R35 NS132179
6 · The paper itself

Abstract

We recently reported that the loss of oligodendrocyte metabolic support through the lactate and pyruvate transporter Monocarboxylate Transporter 1 (MCT1) is well tolerated into adulthood. Only with advanced aging did we observe axonal degeneration and hypomyelination due to the loss of MCT1 from oligodendroglia lineage cells. MCT1 is also expressed by other glial subtypes, such as astrocytes and endothelial cells where it has been suggested to be essential for learning and memory tasks. However, the importance of MCT1 in these cell types for long-term axonal metabolic support is still unknown. We therefore addressed whether the conditional loss of MCT1 from either of these cell types would lead to widespread axonal degeneration with aging. Using a conditional null approach, similar to what was used for oligodendrocyte MCT1 depletion, we observed that the conditional knockout of MCT1 from either astrocytes or endothelial cells did not cause neuronal injury. On the other hand, inducible ubiquitous depletion of MCT1 causes late-onset axonal degeneration, comparable with what was observed in our previous study using the oligodendrocyte lineage MCT1 null mice. Notably, the loss of astrocytic MCT1 does not cause late-onset neurodegeneration. Ubiquitous MCT1 deletion, however, causes axonal degeneration, suggesting that oligodendrocytes and potentially other cells are more prominent drivers of MCT1-mediated metabolic support of neurons. In summary, we conclude that unlike oligodendrocyte MCT1, astrocyte MCT1 is not an essential driver of astrocyte-mediated axonal energy homeostasis with aging.

Indexed as

AstrocytesAxonsMonocarboxylic Acid TransportersNerve DegenerationSymportersAgingAnimalsMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicMonocarboxylate Transport Protein 1OligodendrogliaPhenotypeMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersSymportersastrocyteaxondegenerationlactatemetabolismmonocarboxylate transporter 1

Identifiers

PMID41331335
PMCPMC12673003

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.