Evidence map›Paper›PMID 37952157›Full record

ArticleCell reports2023

Skeletal muscle TFEB signaling promotes central nervous system function and reduces neuroinflammation during aging and neurodegenerative disease.

Ian Matthews, Allison Birnbaum, Anastasia Gromova, Amy W Huang, Kailin Liu, Eleanor A Liu, Kristen Coutinho, Megan McGraw, Dalton C Patterson, Macy T Banks and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
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

27 citing papers in PubMed, 31 citations in OpenAlex.

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  12. Form and function of actin impacts actin health and aging.bioRxiv : the preprint server for biology · 2025
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  19. Enhancement of physiology via adaptive transcription.Pflugers Archiv : European journal of physiology · 2025
    Review
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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

21 authors at 8 institutions in 1 country.

Ian MatthewsLeonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90007, USA.
Allison BirnbaumLeonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90007, USA.
Anastasia GromovaDepartment of Pathology and Laboratory Medicine, UCI Institute for Neurotherapeutics, University of California, Irvine, Irvine, CA 92697, USA.
Amy W HuangLeonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90007, USA.
Kailin LiuLeonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90007, USA.
Eleanor A LiuLeonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90007, USA.
Kristen CoutinhoComprehensive Diabetes Center, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Megan McGrawDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Dalton C PattersonDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Macy T BanksDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Amber C NoblesDepartment of Neurology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Nhat NguyenDepartment of Pathology and Laboratory Medicine, UCI Institute for Neurotherapeutics, University of California, Irvine, Irvine, CA 92697, USA.
Gennifer E MerrihewDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Lu WangDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195, USA.
Eric BaeuerleDepartment of Pharmacology, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Barshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Geriatric Research, Education and Clinical Center, South Texas Veterans Health Care Network, San Antonio, TX 78229, USA.
Elizabeth FernandezDepartment of Pharmacology, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Barshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio, San Antonio, TX 78229, USA; Geriatric Research, Education and Clinical Center, South Texas Veterans Health Care Network, San Antonio, TX 78229, USA.
Nicolas MusiDepartment of Medicine, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Michael J MacCossDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Helen C MirandaDepartment of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; RNA Center, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Albert R La SpadaDepartment of Pathology and Laboratory Medicine, UCI Institute for Neurotherapeutics, University of California, Irvine, Irvine, CA 92697, USA; Department of Neurology and Department of Biological Chemistry, UCI Institute for Neurotherapeutics, University of California, Irvine, Irvine, CA 92697, USA. Electronic address: alaspada@uci.edu.
Constanza J CortesLeonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90007, USA. Electronic address: cjc_149@usc.edu.
University of Southern California · USUniversity of Alabama at Birmingham · USUniversity of California, Irvine · USUniversity of Washington · USCase Western Reserve University · USCedars-Sinai Medical Center · USThe University of Texas at San Antonio · USThe University of Texas Health Science Center at San Antonio · US

Funding

TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JAMES FLOYD NELSON · 1995 to 2026
$30.6M
University of Washington Nathan Shock Center of Excellence in the Basic Biology of AgingP30AG013280 · NIA · UNIVERSITY OF WASHINGTON · PI Michael MacCoss · 1995 to 2026
$27.1M
USC Geroscience Training in the Biology of AgingT32AG052374 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Sean P CURRAN · 2016 to 2026
$5.3M
Molecular genetic regulation of autophagy in health and neurodegenerative diseaseR01AG033082 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LA SPADA, ALBERT R · 2009 to 2019
$4.0M
MAP4K3 regulation of cellular stress response pathways in health and diseaseRF1AG033082 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI LA SPADA, ALBERT R · 2022 to 2025
$3.3M
Enhanced skeletal muscle proteostasis as a determinant of CNS protein quality control and neural function in the aging brainRF1AG057264 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CORTES, CONSTANZA JAVIERA, LA SPADA, ALBERT R · 2017 to 2021
$2.7M
Exercise-Associated Signaling Against CNS Aging and Alzheimer's DiseaseR01AG077536 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Constanza Javiera Cortes · 2022 to 2026
$2.4M
Study of AR transcriptional network in stem cell model of SBMAR01NS121374 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI MIRANDA, HELEN C · 2021 to 2025
$2.0M
Study of SBMA mutant AR transcriptional network in stem cell-derived motor neurons and skeletal muscleK01NS116119 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI MIRANDA, HELEN C · 2020 to 2024
$832k
Enhanced Skeletal Muscle Proteostasis as a Modulator of Alzheimer's DiseaseR03AG063215 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CORTES, CONSTANZA JAVIERA · 2019 to 2020
$309k
FASEB SRC on Yeast Chromosome Structure, Replication and SegregationR13ES022140 · NIEHS · FEDERATION OF AMER SOC FOR EXPER BIOLOGY · PI KEENEY, SCOTT · 2012 to 2012
$8k
NIA NIH HHS P30 AG013280NIA NIH HHS P30 AG013319NIA NIH HHS R01 AG033082NIA NIH HHS R01 AG077536NIA NIH HHS R03 AG063215NIA NIH HHS RF1 AG033082NIA NIH HHS RF1 AG057264NIA NIH HHS T32 AG052374NIEHS NIH HHS R13 ES022140NINDS NIH HHS K01 NS116119NINDS NIH HHS R01 NS121374
6 · The paper itself

Abstract

Skeletal muscle has recently arisen as a regulator of central nervous system (CNS) function and aging, secreting bioactive molecules known as myokines with metabolism-modifying functions in targeted tissues, including the CNS. Here, we report the generation of a transgenic mouse with enhanced skeletal muscle lysosomal and mitochondrial function via targeted overexpression of transcription factor E-B (TFEB). We discovered that the resulting geroprotective effects in skeletal muscle reduce neuroinflammation and the accumulation of tau-associated pathological hallmarks in a mouse model of tauopathy. Muscle-specific TFEB overexpression significantly ameliorates proteotoxicity, reduces neuroinflammation, and promotes transcriptional remodeling of the aged CNS, preserving cognition and memory in aged mice. Our results implicate the maintenance of skeletal muscle function throughout aging in direct regulation of CNS health and disease and suggest that skeletal muscle originating factors may act as therapeutic targets against age-associated neurodegenerative disorders.

Indexed as

Neurodegenerative DiseasesAgingAnimalsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCentral Nervous SystemMiceMice, TransgenicMuscle, SkeletalNeuroinflammatory DiseasesTranscription FactorsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsTranscription FactorsagingbrainCP: NeuroscienceexercisemuscleneurodegenerationtauTFEB

Identifiers

PMID37952157
PMCPMC10841857
OpenAlexW4388583270

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.