Abstract |
Metabolic reprogramming of immune cells has been proven to be important for systemic lupus erythematosus (SLE). This study aims to understand the role of SLC7A5, an amino acid transporter, in SLE. We analyzed SLC7A5 mRNA expression of SLE patients compared to healthy controls using GEO database, and found that it was increased in CD4+ T cells and CD19+ B cells. We then confirmed the expression up-regulation using flow cytometry and found that the proportion of SLC7A5+ cells and its expression were increased in peripheral blood T and B cells from SLE patients. Importantly, SLC7A5 expression in T and B cells was positively correlated with blood urea nitrogen and serum creatinine. Therefore, we conclude that SLC7A5, up-regulating in circulating T and B cells, correlates with kidney function, suggesting its potential role in mediating renal damage in SLE, which provides novel insight into SLE pathogenesis and provides a potential biomarker for disease.
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Authors | Juan Tian, Xiaowei Li, Yiru Jiang, Feng Gao, Bomiao Ju, Jiayue Chen, Wenhua Zhu, Lan He, Liesu Meng, Shemin Lu |
Journal | Clinical immunology (Orlando, Fla.)
(Clin Immunol)
Vol. 237
Pg. 108987
(04 2022)
ISSN: 1521-7035 [Electronic] United States |
PMID | 35346864
(Publication Type: Journal Article)
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Copyright | Copyright © 2022 Elsevier Inc. All rights reserved. |
Chemical References |
- Antigens, CD19
- Large Neutral Amino Acid-Transporter 1
- SLC7A5 protein, human
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Topics |
- Antigens, CD19
- B-Lymphocytes
- Flow Cytometry
- Humans
- Kidney
(pathology)
- Large Neutral Amino Acid-Transporter 1
(genetics)
- Lupus Erythematosus, Systemic
(complications)
- T-Lymphocytes
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