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  • Physiological DNA damage promotes functional endoreplication of mammary gland alveolar cells during lactation.

Physiological DNA damage promotes functional endoreplication of mammary gland alveolar cells during lactation.

Nature communications (2024-04-17)
Rut Molinuevo, Julien Menendez, Kora Cadle, Nabeela Ariqat, Marie Klaire Choy, Cayla Lagousis, Gwen Thomas, Catherine Strietzel, J W Bubolz, Lindsay Hinck
ABSTRACT

Lactation insufficiency affects many women worldwide. During lactation, a large portion of mammary gland alveolar cells become polyploid, but how these cells balance the hyperproliferation occurring during normal alveologenesis with terminal differentiation required for lactation is unknown. Here, we show that DNA damage accumulates due to replication stress during pregnancy, activating the DNA damage response. Modulation of DNA damage levels in vivo by intraductal injections of nucleosides or DNA damaging agents reveals that the degree of DNA damage accumulated during pregnancy governs endoreplication and milk production. We identify a mechanism involving early mitotic arrest through CDK1 inactivation, resulting in a heterogeneous alveolar population with regards to ploidy and nuclei number. The inactivation of CDK1 is mediated by the DNA damage response kinase WEE1 with homozygous loss of Wee1 resulting in decreased endoreplication, alveologenesis and milk production. Thus, we propose that the DNA damage response to replication stress couples proliferation and endoreplication during mammary gland alveologenesis. Our study sheds light on mechanisms governing lactogenesis and identifies non-hormonal means for increasing milk production.

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