Neuron-specific isoform of PGC-1α regulates neuronal metabolism and brain aging

The brain is a high-energy tissue, and although aging is associated with dysfunctional inflammatory and neuron-specific functional pathways, a direct connection to metabolism is not established. Here, we show that isoforms of mitochondrial regulator PGC-1α are driven from distinct brain cell-type specific promotors, repressed with aging, and integral in coordinating metabolism and growth signaling. Transcriptional and proteomic profiles of cortex from male adult, middle age, and advanced age mice reveal an aging metabolic signature linked to PGC-1α. In primary culture, a neuron-exclusive promoter produces the functionally dominant isoform of PGC-1α. Using growth repression as a challenge, we find that PGC-1α is regulated downstream of GSK3β independently across promoters. Broad cellular metabolic consequences of growth inhibition observed in vitro are mirrored in vivo, including activation of PGC-1α directed programs and suppression of aging pathways. These data place PGC-1α centrally in a growth and metabolism network directly relevant to brain aging.

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Publication Details

Journal
Nature Communications
Published
2025-02-28
DOI
https://doi.org/10.1038/s41467-025-57363-y
Citations
11
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
12.81

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article

Neuron-specific isoform of PGC-1α regulates neuronal metabolism and brain aging

Dylan C. Souder, Timothy W. Rhoads, Kevin W. Eliceiri, Darcie L. Moore et al.
11 citations
Nature Communications
Adipose Tissue and Metabolism
12.81
article

Neuron-specific isoform of PGC-1α regulates neuronal metabolism and brain aging

Dylan C. Souder, Timothy W. Rhoads, Kevin W. Eliceiri, Darcie L. Moore, Eric R. McGregor, Tiaira J. Porter, Luigi Puglielli, Rozalyn M. Anderson, Josef P. Clark
article en
11 citations

Abstract

The brain is a high-energy tissue, and although aging is associated with dysfunctional inflammatory and neuron-specific functional pathways, a direct connection to metabolism is not established. Here, we show that isoforms of mitochondrial regulator PGC-1α are driven from distinct brain cell-type specific promotors, repressed with aging, and integral in coordinating metabolism and growth signaling. Transcriptional and proteomic profiles of cortex from male adult, middle age, and advanced age mice reveal an aging metabolic signature linked to PGC-1α. In primary culture, a neuron-exclusive promoter produces the functionally dominant isoform of PGC-1α. Using growth repression as a challenge, we find that PGC-1α is regulated downstream of GSK3β independently across promoters. Broad cellular metabolic consequences of growth inhibition observed in vitro are mirrored in vivo, including activation of PGC-1α directed programs and suppression of aging pathways. These data place PGC-1α centrally in a growth and metabolism network directly relevant to brain aging.

Nature CommunicationsVol. 16(1)
University of Wisconsin–Madison (US), Geriatric Research Education and Clinical Center (US), William S. Middleton Memorial Veterans Hospital (US)
Simons Foundation, National Institute on Aging
Affordable and clean energy
Openalex Percentile: Top 1%
Adipose Tissue and Metabolism
12.81
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