Nature communications · 2025
Testosterone exacerbates neutrophilia and cardiac injury in myocardial infarction via actions in bone marrow.
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Svedlund Eriksson Elin, Lantero Rodriguez Marta, Halvorsen Bente, Johansson Inger, Mårtensson Anna K F, Wilhelmson Anna S, Huse Camilla, Ueland Thor, Aukrust Pål, Broch Kaspar, Gullestad Lars, Amundsen Brage Høyem, Andersen Geir Øystein, Karlsson Mikael C I, Hagberg Thulin Malin, Camponeschi Alessandro, Trompet Dana, Hammarsten Ola, Redfors Björn, Borén Jan, Omerovic Elmir, Levin Malin C, Chagin Andrei S, Dahl Tuva B, Tivesten Åsa
Аннотация
Men develop larger infarct sizes than women after a myocardial infarction (MI), but the mechanism underlying this sex difference is unknown. Here, we demonstrated that blood neutrophil counts post-MI were higher in male than female mice. Castration-induced testosterone deficiency reduced blood neutrophil counts to the level in females and increased survival post-MI. These effects were mimicked by Osterix-directed ablation of the androgen receptor in bone marrow (BM). Mechanistically, androgens downregulated the leukocyte retention factor CXCL12 in BM stromal cells. Post-hoc analysis of clinical trial data showed that neutrophilia was greater in men than women after reperfusion of first-time ST-elevation MI, and tocilizumab, an interleukin-6 receptor inhibitor, reduced blood neutrophil counts and infarct size to a greater extent in men than women. Our work reveals a previously unknown mechanism connecting testosterone with neutrophilia and MI injury via BM and identifies the importance of considering sex when developing anti-inflammatory strategies to treat MI.