ER remodelling is a feature of ageing and depends on ER-phagy

The endoplasmic reticulum (ER) comprises an array of subdomains, each defined by a characteristic structure and function. Although altered ER processes are linked to age-onset pathogenesis, it is unclear whether shifts in ER structure or dynamics underlie these functional changes. Here we establish ER structural and functional remodelling as a conserved feature of ageing across yeast, Caenorhabditis elegans and mammals. Focusing on C. elegans as the exemplar of metazoan ageing, we reveal striking age-related reductions in ER volume across diverse tissues and a morphological shift from rough sheets to tubular ER. This morphological transition corresponds with large-scale shifts in ER proteome composition from protein synthesis to lipid metabolism, a phenomenon conserved in mammalian tissues. We show that Atg8 and ULK1-dependent ER-phagy drives age-associated ER remodelling through tissue-specific factors, including the previously uncharacterized ER-phagy regulator TMEM-131 and the IRE-1-XBP-1 branch of the unfolded protein response. Providing support for a model where ER remodelling is adaptive, diverse lifespan-extending paradigms downscale and remodel ER morphology throughout life. Furthermore, mTOR-dependent lifespan extension in yeast and worms requires ER-phagy, indicating that ER remodelling is a proactive and protective response during ageing. These results reveal ER-phagy and ER dynamics as pronounced, underappreciated mechanisms of both normal ageing and age-delaying interventions.

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Publication Details

Journal
Nature Cell Biology
Published
2026-02-02
DOI
https://doi.org/10.1038/s41556-025-01860-1
Citations
1
Primary Topic
Endoplasmic Reticulum Stress and Disease
Type
article
Field-Weighted Citation Impact
23.07
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article

ER remodelling is a feature of ageing and depends on ER-phagy

Elizabeth M. Ruark, Natalie Wallace, Lauren P. Jackson, Jason A. MacGurn et al.
1 citations
Nature Cell Biology
Endoplasmic Reticulum Stress and Disease
23.07
article

ER remodelling is a feature of ageing and depends on ER-phagy

Elizabeth M. Ruark, Natalie Wallace, Lauren P. Jackson, Jason A. MacGurn, Andrew W. Folkmann, Kristopher Burkewitz, Matthias C. Truttmann, Stedman Stephens, Nicholas D. Urban, Rafael Arrojo e Drigo, Brennen Keuchel, Eric K. F. Donahue, Derek J. Johnson, Mark H. Ellisman, Li Peng, Nathaniel L. Hepowit, Alexandra G. Mulligan
article en
1 citations

Abstract

The endoplasmic reticulum (ER) comprises an array of subdomains, each defined by a characteristic structure and function. Although altered ER processes are linked to age-onset pathogenesis, it is unclear whether shifts in ER structure or dynamics underlie these functional changes. Here we establish ER structural and functional remodelling as a conserved feature of ageing across yeast, Caenorhabditis elegans and mammals. Focusing on C. elegans as the exemplar of metazoan ageing, we reveal striking age-related reductions in ER volume across diverse tissues and a morphological shift from rough sheets to tubular ER. This morphological transition corresponds with large-scale shifts in ER proteome composition from protein synthesis to lipid metabolism, a phenomenon conserved in mammalian tissues. We show that Atg8 and ULK1-dependent ER-phagy drives age-associated ER remodelling through tissue-specific factors, including the previously uncharacterized ER-phagy regulator TMEM-131 and the IRE-1-XBP-1 branch of the unfolded protein response. Providing support for a model where ER remodelling is adaptive, diverse lifespan-extending paradigms downscale and remodel ER morphology throughout life. Furthermore, mTOR-dependent lifespan extension in yeast and worms requires ER-phagy, indicating that ER remodelling is a proactive and protective response during ageing. These results reveal ER-phagy and ER dynamics as pronounced, underappreciated mechanisms of both normal ageing and age-delaying interventions.

Nature Cell BiologyVol. 28(3)
Vanderbilt University (US), University of Michigan (US), University of California San Diego (US)
Openalex Percentile: Top 2%
Endoplasmic Reticulum Stress and Disease
23.07
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