MLKL deficiency elevates testosterone production in male mice independently of necroptotic functions

Cell Death Dis. 2024 Nov 21;15(11):851. doi: 10.1038/s41419-024-07242-z.

Abstract

Mixed lineage kinase domain-like (MLKL) is a pseudokinase, best known for its role as the terminal effector of the necroptotic cell death pathway. MLKL-mediated necroptosis has long been linked to various age-related pathologies including neurodegeneration, atherosclerosis and male reproductive decline, however many of these attributions remain controversial. Here, we investigated the role of MLKL and necroptosis in the adult mouse testis: an organ divided into sperm-producing seminiferous tubules and the surrounding testosterone-producing interstitium. We find that sperm-producing cells within seminiferous tubules lack expression of key necroptotic mediators and thus are resistant to a pro-necroptotic challenge. By comparison, coordinated expression of the necroptotic pathway occurs in the testicular interstitium, rendering cells within this compartment, especially the lysozyme-positive macrophages, vulnerable to necroptotic cell death. We also uncover a non-necroptotic role for MLKL in regulating testosterone levels. Thus, MLKL serves two roles in the mouse testes - one involving the canonical response of macrophages to necroptotic insult, and the other a non-canonical function in male reproductive hormone control.

MeSH terms

  • Animals
  • Macrophages / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Necroptosis*
  • Protein Kinases* / metabolism
  • Spermatozoa / metabolism
  • Testis* / metabolism
  • Testosterone* / metabolism

Substances

  • Testosterone
  • MLKL protein, mouse
  • Protein Kinases