Replication stress responses in human lymphocytes change sex-specifically during aging

The varying incidence of aging-related diseases and the gender gap in life expectancy suggest differences in the aging process between the sexes. Yet, little is known about sex-specific differences in genomic instability, a key factor in aging. Here, we analyzed DNA damage responses (DDRs) in cycling peripheral blood lymphocytes (PBL) and hematopoietic stem and progenitor cells (HSPC) from female and male donors of different age, focusing on replication stress. Transcriptomics revealed striking sex-dependent expression changes in DDR pathways during aging. Particularly, various DDR components, involved in DNA repair and replication fork remodeling, were upregulated with age in men. In older women, functional analysis indicated reduced activity of the Fanconi anemia pathway. Analyses of replication dynamics, PCNA ubiquitination, translesion synthesis (TLS)-polymerase signals, and sensitivities to TLS-polymerase inhibitors indicate a shift from fork remodeling to fast TLS inducing nonclassical replication stress. While replication dynamics were unaltered and replication stress rather reduced, PBL from older men were highly dependent on PARP activity. In conclusion, our findings revealed sex-specific strategies to cope with replication stress in PBL from older individuals, namely through DNA damage tolerance pathway switching in women and PARP activation in men, differentially contributing to the decline of genomic stability with age.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-06-06
DOI
https://doi.org/10.1093/nar/gkaf498
Citations
1
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.80

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article

Replication stress responses in human lymphocytes change sex-specifically during aging

Helmut Pospiech, Miriam Deniz, Lisa Wiesmüller, Michael Milyavsky et al.
1 citations
Nucleic Acids Research
Immune Cell Function and Interaction
0.80
article

Replication stress responses in human lymphocytes change sex-specifically during aging

Helmut Pospiech, Miriam Deniz, Lisa Wiesmüller, Michael Milyavsky, Stephanie Biber, Friedemann Zengerling, Marco Groth, Melanie Rall-Scharpf, Halvard Bonig, Stefanie Braig, Philipp Koch, Arne Sahm, Dominik Schlotter, Dhayana Dallmeier, Benedikt Heitmeir, Karol Szafranski, Bryan A. Castaño
article en
1 citations

Abstract

The varying incidence of aging-related diseases and the gender gap in life expectancy suggest differences in the aging process between the sexes. Yet, little is known about sex-specific differences in genomic instability, a key factor in aging. Here, we analyzed DNA damage responses (DDRs) in cycling peripheral blood lymphocytes (PBL) and hematopoietic stem and progenitor cells (HSPC) from female and male donors of different age, focusing on replication stress. Transcriptomics revealed striking sex-dependent expression changes in DDR pathways during aging. Particularly, various DDR components, involved in DNA repair and replication fork remodeling, were upregulated with age in men. In older women, functional analysis indicated reduced activity of the Fanconi anemia pathway. Analyses of replication dynamics, PCNA ubiquitination, translesion synthesis (TLS)-polymerase signals, and sensitivities to TLS-polymerase inhibitors indicate a shift from fork remodeling to fast TLS inducing nonclassical replication stress. While replication dynamics were unaltered and replication stress rather reduced, PBL from older men were highly dependent on PARP activity. In conclusion, our findings revealed sex-specific strategies to cope with replication stress in PBL from older individuals, namely through DNA damage tolerance pathway switching in women and PARP activation in men, differentially contributing to the decline of genomic stability with age.

Nucleic Acids ResearchVol. 53(11)
Goethe University Frankfurt (DE), Tel Aviv University (IL), Zimmer Biomet (Netherlands) (NL), Universität Ulm (DE), German Red Cross (DE), Institute for Transfusion Medicine (US), Düsseldorf University Hospital (DE), Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) (DE), Agaplesion Bethesda Klinik (DE), Life Science Center Düsseldorf (Germany) (DE), Heinrich Heine University Düsseldorf (DE)
Deutsche Forschungsgemeinschaft
Gender equality
Openalex Percentile: Top 27%
Immune Cell Function and Interaction
0.80
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