The expression of System Xc-/ GSH / GPX4 ferroptosis pathway in peripheral blood mononuclear cells of rheumatoid arthritis patients and its effect on the secretion of inflammatory factors
10.19405/j.cnki.issn1000-1492.2024.01.011
- Author:
Can Liu
1
,
2
;
Wukai Ma
3
;
Changming Chen
3
;
Yang An
3
;
Zong Jiang
3
;
Hai Huang
1
,
4
Author Information
1. Dept of Clinical Biochemistry and Molecular Biology，School of Clinical Laboratory Science，Guizhou Medical University，Guiyang 550004
2. Dept of Rheumatology and Immunology，The Second Affiliated Hospital of Guizhou University of Chinese Medicine，Guiyang 550004
3. Dept of Rheumatology and Immunology，The Second Affiliated Hospital of Guizhou University of Chinese Medicine，Guiyang 550004
4. Center for Clinical Laboratory， The Affiliated Hospital of Guizhou Medical University，Guiyang 550004
- Publication Type:Journal Article
- Keywords:
rheumatoid arthritis;
peripheral blood mononuclear cells;
ferroptosis;
System Xc-/ GSH / GPX4
- From:
Acta Universitatis Medicinalis Anhui
2024;59(1):64-70
- CountryChina
- Language:Chinese
-
Abstract:
Objective :To investigate the expression of genes and proteins in the peripheral blood mononuclear cell ( PBMC) cystine / glutamate antiporter system (System Xc-) / glutathione ( GSH) / glutathione peroxidase 4 ( GPX4) ferroptosis pathway and its influence on inflammatory factors in patients with rheumatoid arthritis ( RA) ．
Methods :30 patients with RA and 30 healthy participants were enrolled．PBMCs were isolated using Ficoll-hypaque density gradient centrifugation．The cells were categorized into the healthy control，RA，ferroptosis inhibitor，ferroptosis in- ducer group．The cell viability was checked using the cell counting kit-8 ( CCK-8) method．Intracellular Fe2 + rela- tive fluorescence intensity and reactive oxygen species (ROS) levels were detected using the FerroOrange and Di- hydroethidium (DHE) fluorescent probes，respectively．Western blot and real-time quantitative PCR (qPCR) de- tected the expression of nuclear factor erythroid 2-related factor 2 ( Nrf2 ) ，solute carrier family 7 member 11 (SLC7A11) ，GPX4 proteins and mRNA．And the flow cytometry quantified the levels of tumor necrosis factor α (TNF-α) ，Interleukin (IL) -1，and IL-6 in the supernatant of each cell group.
Results : Compared to the healthy control group，the RA group showed a significantly increased Fe2 + concentration and elevated ROS levels，reduced expression of Nrf2，SLC7A11 and GPX4 proteins and mRNA，and increased contents of TNF-α , IL-1 and IL-6 in PBMC supernatant，and the differences were statistically significant．The concentration of Fe2 + and ROS levels in the inhibitor group were lower than those in the RA group，the proteins expressions of Nrf2，SLC7A11 and GPX4 increased，the mRNA expressions of SLC7A11 and GPX4 increased，the content of IL-6 in the PBMC supernatant decreased but the content of TNF-α increased，and the differences were statistically significant．In contrast，the in- ducer group，when compared to the RA group，displayed increased ROS levels，reduced expression of SLC7A11 protein and mRNA and decreased expression of Nrf2 protein，and the contents of TNF-α and IL-1 in the PBMC su- pernatant increased，but the expression of GPX4 protein increased ，and the differences were statistically signifi- cant．The inducer group，compared to the RA group，showed increased cell viability，and the difference was statis-
tically significant (P＜0. 000 1) ．
Conclusion : The presence of ferroptosis in PBMC in RA patients，inhibiting or inducing PBMC ferroptosis in RA patients，will inhibit or promote the secretion of inflammatory factors．Inhibition of PBMC ferroptosis in RA patients may be helpful in the treatment of RA.
- Full text:2024062416252567791类风湿关节炎患者外周血单个...达及其对炎症因子分泌的影响_刘灿.pdf
