An in vivo resource of age-regulated C. elegans intestinal secretory-pathway proteins highlights secreted enzymes associated with lifespan regulation

Secreted proteins are essential to modulate homeostasis in the extracellular space and facilitate communication to distal cells or tissues. Yet, the identity and functional importance of extracellular proteins in aging have been understudied. Here we use proximity labeling followed by quantitative proteomics to systematically characterize proteins along the intestinal secretory pathway in C. elegans, focusing on secreted proteins. We identify intestine-secreted proteins that are modulated with age, and validate the secretion of these proteins in vivo. One of these secreted proteins, ACP7, is well conserved in humans, and its overexpression extends lifespan in a secretion-dependent manner. Interestingly, we find that ACP7 acts as a secreted phosphatase in the extracellular space. Finally, we identify additional proteins along the secretory pathway that regulate lifespan. Our systematic characterization of tissue-specific secreted proteins during aging uncovers conserved proteins that impact lifespan and highlights extracellular enzymes associated with lifespan regulation.

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Journal
Cell Reports
Published
2026-08-27
DOI
https://doi.org/10.1016/j.celrep.2026.117902
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
0.00

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article

An in vivo resource of age-regulated C. elegans intestinal secretory-pathway proteins highlights secreted enzymes associated with lifespan regulation

Brandon Ameglio, Aleksandra Levina, Nicole Haseley, Karen L. Artiles et al.
Cell Reports
Genetics, Aging, and Longevity in Model Organisms
article

An in vivo resource of age-regulated C. elegans intestinal secretory-pathway proteins highlights secreted enzymes associated with lifespan regulation

Brandon Ameglio, Aleksandra Levina, Nicole Haseley, Karen L. Artiles, Uche N. Medoh, F. McCarthy, Katharina Papsdorf, Daniel Richard, Olivia Y. Zhou, Anne Brunet, Eric Sun, Andy Hims, Aleksandra Tsenter, Jason W. Miklas, Monther Abu-Remaileh, Joshua E. Elias
article en

Abstract

Secreted proteins are essential to modulate homeostasis in the extracellular space and facilitate communication to distal cells or tissues. Yet, the identity and functional importance of extracellular proteins in aging have been understudied. Here we use proximity labeling followed by quantitative proteomics to systematically characterize proteins along the intestinal secretory pathway in C. elegans, focusing on secreted proteins. We identify intestine-secreted proteins that are modulated with age, and validate the secretion of these proteins in vivo. One of these secreted proteins, ACP7, is well conserved in humans, and its overexpression extends lifespan in a secretion-dependent manner. Interestingly, we find that ACP7 acts as a secreted phosphatase in the extracellular space. Finally, we identify additional proteins along the secretory pathway that regulate lifespan. Our systematic characterization of tissue-specific secreted proteins during aging uncovers conserved proteins that impact lifespan and highlights extracellular enzymes associated with lifespan regulation.

Cell ReportsVol. 45(9)
Cardiovascular Institute of the South (US), Chan Zuckerberg Biohub San Francisco (US), Stanford University (US)
Larry L. Hillblom Foundation, Chan Zuckerberg Initiative, National Institute on Aging
Zero hunger
Openalex Percentile: Top 15%
Genetics, Aging, and Longevity in Model Organisms
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