Aging disrupts spatiotemporal coordination in the cycling murine ovary

Throughout the female reproductive lifespan, the ovary undergoes hundreds of cycles of follicle development, ovulation and tissue regeneration. How aging disrupts the coordination of such precise, multicellular interactions across time and space is not well understood. Using Slide-seq, a near-cellular spatial transcriptomics method, here we profile 22 mouse ovaries across the reproductive cycle and chronological ages, capturing 610,620 spots across 69 spatial profiles. We develop a novel segmentation pipeline to examine the multicellular dynamics of 358 oocytes, 668 follicles and 236 corpora lutea to find that aging impairs the spatial and temporal coordination required for folliculogenesis even before reproductive cycles cease. These disruptions are characterized by altered immune cell dynamics, inflammatory signaling and global tissue disorganization, which impair the cyclic remodeling required for ovarian function. Our findings reveal how multicellular niches orchestrate ovarian function and demonstrate that age-related breakdown in tissue organization precedes the end of fertility.

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Publication Details

Journal
Nature Aging
Published
2026-06-17
DOI
https://doi.org/10.1038/s43587-026-01140-z
Primary Topic
Reproductive Biology and Fertility
Type
article
Field-Weighted Citation Impact
0.00

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article

Aging disrupts spatiotemporal coordination in the cycling murine ovary

David S. Fischer, Andrew Minagar, Giovanni Marrero, Tammy C. T. Lan et al.
Nature Aging
Reproductive Biology and Fertility
article

Aging disrupts spatiotemporal coordination in the cycling murine ovary

David S. Fischer, Andrew Minagar, Giovanni Marrero, Tammy C. T. Lan, Jennifer L. Garrison, Pardis C. Sabeti, María Martín Fuentes, Alex K. Shalek, Ruth Raichur, Hattie Chung, Alison Kochersberger, Fei Chen, Vipin Kumar, Sophia Szady, Radiana Simeonova, Irving Barrera, Hien Tran, Sarah Mangiameli, Ashley Helmuth
article en

Abstract

Throughout the female reproductive lifespan, the ovary undergoes hundreds of cycles of follicle development, ovulation and tissue regeneration. How aging disrupts the coordination of such precise, multicellular interactions across time and space is not well understood. Using Slide-seq, a near-cellular spatial transcriptomics method, here we profile 22 mouse ovaries across the reproductive cycle and chronological ages, capturing 610,620 spots across 69 spatial profiles. We develop a novel segmentation pipeline to examine the multicellular dynamics of 358 oocytes, 668 follicles and 236 corpora lutea to find that aging impairs the spatial and temporal coordination required for folliculogenesis even before reproductive cycles cease. These disruptions are characterized by altered immune cell dynamics, inflammatory signaling and global tissue disorganization, which impair the cyclic remodeling required for ovarian function. Our findings reveal how multicellular niches orchestrate ovarian function and demonstrate that age-related breakdown in tissue organization precedes the end of fertility.

Nature AgingVol. 6(6)
Broad Institute (US), University of Southern California (US), Buck Institute for Research on Aging (US), Howard Hughes Medical Institute (US), Harvard University (US), Austrian Research Institute for Artificial Intelligence (AT), University of California, San Francisco (US), Ragon Institute of MGH, MIT and Harvard (US), Yale University (US), Yale New Haven Health System (US), Cardiovascular Research Center (BR), Massachusetts Institute of Technology (US), Medical University of Vienna (AT)
Yale University, Broad Institute, National Institute of General Medical Sciences
Zero hunger
Openalex Percentile: Top 7%
Reproductive Biology and Fertility
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