[MPV17 inhibits iron overload-induced ferroptosis of splenic CD3+ T cells in mice by blocking ERK pathway]
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Updated: May 12, 2026

Ferritinophagy: Assessing the Selective Degradation of Iron by Autophagy in Human Fibroblasts
Published on: February 23, 2024
Tao Xu1, Wenjun Jing2, Guilan Chen3
1Instrumental Analysis Center of QAU, Qingdao 266109, China.
Abstract:
Objective This work aimed to explore the effect of iron overload on splenic injury and the role of MPV17 in the ferroptosis of splenic CD3+ T cells from mice subjected to iron overload. Methods Mice were randomly divided into normal diet group, high-iron diet group, high-iron diet combined with Fer-1 treatment group, and high-iron diet combined with adenovirus harboring MPV17 injection group, with 5 mice in each group. After treatment for 8 weeks, mice spleens were harvested and fixed; Histological section and HE staining were performed to observe the structures of the spleens; Cell death of CD3+ T cells was detected by propidium iodide (PI) staining; The lipid peroxidation levels were detected by C11 BODIPY581/591 staining; The mRNA levels of Solute carrier family 7 member 11 (SLC7A11) and prostaglandin-endoperoxide synthase 2 (PTGS2) were detected by qPCR assays; The macrophage phenotype-switching (M1/M2) were detected by flow cytometry; The levels of TNF-α, IL-1β and IL-6 were measured by ELISA assays. Moreover, high-iron diet combined with extracellular signal-regulated kinase (ERK) inhibitor treatment group, ERK agonist treatment group, β-gal combined with ERK agonist treatment group, and MPV17 overexpression combined with ERK agonist treatment group were added. The protein levels of MPV17, glutathione peroxidase 4 (GPX4) and phosphorylated ERK (p-ERK) were detected by Western blot; The mitochondrial membrane potential was detected by JC-1 staining and flow cytometry. Results Compared with the normal diet group, the red pulps of the mice spleens from the high-iron diet group showed irregular structures and the white pulps were almost missing; Cell death, lipid peroxides, and the expression levels of SLC7A11 and PTGS2 increased; Both the ratio of M1 macrophages to M2 macrophages and the levels of inflammatory factors increased. Fer-1 treatment or overexpression of MPV17 in the high-iron diet mice group partially recovered the irregular structures of the spleens, reduced cell death and lipid peroxides in CD3+ T cells, and decreased the expression levels of SLC7A11 and PTGS2; The ratio of M1/M2 macrophages and the levels of inflammatory factors were decreased. High-iron diet decreased the protein levels of GPX4 while p-ERK were up-regulated. Inhibition of ERK partially recovered the protein levels of GPX4; ERK agonist decreased the protein levels of GPX4; MPV17 inhibited the ERK signaling and partially recovered the protein levels of GPX4 and the decreased mitochondrial membrane potential of CD3+ T induced by ERK activation. Conclusion Iron overload resulted in splenic injury and ferroptosis in the splenic CD3+ T cells; MPV17 prevented splenic injury and ferroptosis of splenic CD3+ T cells of the iron overload mice through blocking ERK signaling pathway.
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.

