Testosterone exacerbates neutrophilia and cardiac injury in myocardial infarction via actions in bone marrow

Nat Commun. 2025 Feb 5;16(1):1142. doi: 10.1038/s41467-025-56217-x.

Abstract

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.

MeSH terms

  • Animals
  • Antibodies, Monoclonal, Humanized
  • Bone Marrow* / pathology
  • Chemokine CXCL12 / metabolism
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myocardial Infarction* / metabolism
  • Myocardial Infarction* / pathology
  • Neutrophils* / metabolism
  • Receptors, Androgen / metabolism
  • Testosterone* / blood

Substances

  • Testosterone
  • Chemokine CXCL12
  • tocilizumab
  • Receptors, Androgen
  • Cxcl12 protein, mouse
  • Antibodies, Monoclonal, Humanized