ETV5 promotes lupus pathogenesis and follicular helper T cell differentiation by inducing osteopontin expression.
Jiho ParkJongeun LeeYunjung HurChan-Johng KimHan Bit KimDahun UmDa Som KimJune-Yong LeeSungjun ParkYoungjae ParkTae-Kyung KimSin-Hyeog ImSung Won KimSeung-Ki KwokYoontae LeePublished in: Proceedings of the National Academy of Sciences of the United States of America (2024)
Follicular helper T (T FH ) cells mediate germinal center reactions to generate high affinity antibodies against specific pathogens, and their excessive production is associated with the pathogenesis of systemic autoimmune diseases such as systemic lupus erythematosus (SLE). ETV5, a member of the ETS transcription factor family, promotes T FH cell differentiation in mice. In this study, we examined the role of ETV5 in the pathogenesis of lupus in mice and humans. T cell-specific deletion of Etv5 alleles ameliorated T FH cell differentiation and autoimmune phenotypes in lupus mouse models. Further, we identified SPP1 as an ETV5 target that promotes T FH cell differentiation in both mice and humans. Notably, extracellular osteopontin (OPN) encoded by SPP1 enhances T FH cell differentiation by activating the CD44-AKT signaling pathway. Furthermore, ETV5 and SPP1 levels were increased in CD4 + T cells from patients with SLE and were positively correlated with disease activity. Taken together, our findings demonstrate that ETV5 is a lupus-promoting transcription factor, and secreted OPN promotes T FH cell differentiation.
Keyphrases
- systemic lupus erythematosus
- disease activity
- acute lymphoblastic leukemia
- transcription factor
- signaling pathway
- rheumatoid arthritis
- rheumatoid arthritis patients
- ankylosing spondylitis
- induced apoptosis
- juvenile idiopathic arthritis
- high fat diet induced
- poor prognosis
- mouse model
- cell proliferation
- pi k akt
- multiple sclerosis
- dna binding
- skeletal muscle
- epithelial mesenchymal transition
- oxidative stress
- long non coding rna
- physical activity
- body mass index
- immune response
- binding protein
- insulin resistance
- cell death
- cell cycle arrest
- genetic diversity