ETV5 promotes lupus pathogenesis and follicular helper T cell differentiation by inducing osteopontin expression

Author:

Park Jiho1,Lee Jongeun1ORCID,Hur Yunjung1,Kim Chan-Johng1,Kim Han Bit1,Um Dahun1,Kim Da Som2,Lee June-Yong3ORCID,Park Sungjun4ORCID,Park Youngjae5,Kim Tae-Kyung1,Im Sin-Hyeog16ORCID,Kim Sung Won7,Kwok Seung-Ki5,Lee Yoontae16ORCID

Affiliation:

1. Department of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, Republic of Korea

2. The Rheumatism Research Center, Catholic Research Institute of Medical Science, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea

3. Department of Microbiology and Immunology, Institute for Immunology and Immunological Diseases, and Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University College of Medicine, Seoul 03722, Republic of Korea

4. Department of Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technology, Daejeon 34114, Republic of Korea

5. Division of Rheumatology, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea

6. Institute for Convergence Research and Education in Advanced Technology, Yonsei University, Seoul 03722, Republic of Korea

7. Department of Otolaryngology-Head and Neck Surgery, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea

Abstract

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.

Funder

National Research Foundation of Korea

Korea Basic Science Institute

Publisher

Proceedings of the National Academy of Sciences

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