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CN 34-1304/RISSN 1674-3679

Volume 27 Issue 12
Dec.  2023
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Article Contents
WU Jun, LI Shangjie, ZHANG Jie, YE Dongqing, NI Jindong. Associations between m6A related-mRNA IFIT5 and systemic lupus erythematosus[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2023, 27(12): 1455-1460. doi: 10.16462/j.cnki.zhjbkz.2023.12.015
Citation: WU Jun, LI Shangjie, ZHANG Jie, YE Dongqing, NI Jindong. Associations between m6A related-mRNA IFIT5 and systemic lupus erythematosus[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2023, 27(12): 1455-1460. doi: 10.16462/j.cnki.zhjbkz.2023.12.015

Associations between m6A related-mRNA IFIT5 and systemic lupus erythematosus

doi: 10.16462/j.cnki.zhjbkz.2023.12.015
Funds:

Guangdong Basic and Applied Basic Research Foundation 2022A1515111042

The National Natural Science Foundation of China 81872693

The National Natural Science Foundation of China 81872687

More Information
  • Corresponding author: YE Dongqing, E-mail: anhuiydq@126.com; NI Jindong, E-mail: nijd-gw@gdmu.edu.cn
  • Received Date: 2023-07-31
  • Rev Recd Date: 2023-10-18
  • Publish Date: 2023-12-10
  •   Objective  N6-methyladenosine (m6A) methylation involved in immuno-inflammatory responses via the regulation of mRNA expression and function is reported, but its limit is in systemic lupus erythematosus (SLE). Therefore, this study will initially explore the associations of m6A-related mRNA expression with SLE.  Methods  Real-time quantitative polymerase chain reaction and western blot were used to validate the expression levels of m6A-related IFIT5in T cells of patients with SLE. Following that, the correlations between IFIT5and clinical characteristics, laboratory parameters and treatment of patients with SLE were analyzed. Further functional experiments were conducted to establish the Jurkat cell lines with silencing IFIT5 for exploration of the alteration of T cells and immune inflammatory cytokines (TNF-α, IL-2, and IL-6).  Results  Compared with normal controls, m6A modification of highly expressed IFIT5 in SLE patients was significantly enhanced. The expression levels of IFIT5 were steadily up-regulated in the T cells of patients with SLE, and were closely associated with the degree of disease activity in patients with SLE. Cell experiments showed that silencing IFIT5 significantly inhibited T cell proliferation and accelerated apoptosis, as well as triggered tumor necrosis factor-alpha (TNF-α) secretion and induced the expression levels of interleukin-2 (IL-2) and interleukin-6 (IL-6).  Conclusion  The high expression level of IFIT5is related to m6A modification, it is also up-regulated in the T cells of patients with SLE, which participate in the immune inflammatory responses of Jurkat cells, and the specific mechanism deserves further study.
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