[MPV17 inhibits iron overload-induced ferroptosis of splenic CD3+ T cells in mice by blocking ERK pathway]

Tao Xu1, Wenjun Jing2, Guilan Chen3

  • 1Instrumental Analysis Center of QAU, Qingdao 266109, China.

Insights

Iron overload causes spleen injury and ferroptosis in splenic CD3+ T cells. MPV17 protein prevents this by blocking the ERK signaling pathway, protecting the spleen.

Area of Science:

  • Immunology
  • Cell Biology
  • Toxicology

Background:

  • Iron overload is linked to various organ injuries.
  • Ferroptosis, a regulated cell death pathway, plays a role in T cell dysfunction.
  • The specific mechanisms of iron overload-induced splenic injury and T cell ferroptosis remain unclear.

Purpose of the Study:

  • To investigate the impact of iron overload on splenic injury.
  • To determine the role of MPV17 in ferroptosis of splenic CD3+ T cells under iron overload conditions.
  • To elucidate the underlying molecular mechanisms, including the extracellular signal-regulated kinase (ERK) signaling pathway.

Main Methods:

  • Mice were subjected to high-iron diets and treated with Fer-1 or MPV17.
  • Spleen histology, CD3+ T cell death (propidium iodide staining), and lipid peroxidation (C11 BODIPY581/591 staining) were assessed.
  • mRNA levels of SLC7A11 and PTGS2, macrophage polarization (M1/M2), and inflammatory cytokines (TNF-α, IL-1β, IL-6) were measured.
  • Protein levels of MPV17, GPX4, and p-ERK were analyzed by Western blot; mitochondrial membrane potential was evaluated using JC-1 staining.

Main Results:

  • High-iron diet induced splenic structural damage, increased CD3+ T cell death, lipid peroxidation, and inflammatory markers.
  • MPV17 overexpression or Fer-1 treatment partially restored spleen structure and reduced ferroptosis markers.
  • Iron overload upregulated p-ERK and downregulated GPX4; MPV17 inhibited ERK signaling, restoring GPX4 levels and mitochondrial function.

Conclusions:

  • Iron overload causes splenic injury and ferroptosis in splenic CD3+ T cells.
  • MPV17 acts as a protective factor against iron overload-induced splenic injury and T cell ferroptosis.
  • MPV17 exerts its protective effects by inhibiting the ERK signaling pathway.