The Protective Effect of Zebularine, an Inhibitor of DNA Methyltransferase, on Renal Tubulointerstitial Inflammation and Fibrosis

Eun Sil Koh, Soojeong Kim, Mina Son, Ji Young Park, Jaehyuk Pyo, Wan Young Kim, Minyoung Kim, Sungjin Chung, Cheol Whee Park, Ho Shik Kim, Seok Joon Shin

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5 Scopus citations

Abstract

Renal fibrosis, the final pathway of chronic kidney disease, is caused by genetic and epigenetic mechanisms. Although DNA methylation has drawn attention as a developing mechanism of renal fibrosis, its contribution to renal fibrosis has not been clarified. To address this issue, the effect of zebularine, a DNA methyltransferase inhibitor, on renal inflammation and fibrosis in the murine unilateral ureteral obstruction (UUO) model was analyzed. Zebularine significantly attenuated renal tubulointerstitial fibrosis and inflammation. Zebularine decreased trichrome, α-smooth muscle actin, collagen IV, and transforming growth factor-β1 staining by 56.2%. 21.3%, 30.3%, and 29.9%, respectively, at 3 days, and by 54.6%, 41.9%, 45.9%, and 61.7%, respectively, at 7 days after UUO. Zebularine downregulated mRNA expression levels of matrix metalloproteinase (MMP)-2, MMP-9, fibronectin, and Snail1 by 48.6%. 71.4%, 31.8%, and 42.4%, respectively, at 7 days after UUO. Zebularine also suppressed the activation of nuclear factor-κB (NF-κB) and the expression of pro-inflammatory cytokines, including tumor necrosis factor-α, interleukin (IL)-1β, and IL-6, by 69.8%, 74.9%, and 69.6%, respectively, in obstructed kidneys. Furthermore, inhibiting DNA methyltransferase buttressed the nuclear expression of nuclear factor (erythroid-derived 2)-like factor 2, which upregulated downstream effectors such as catalase (1.838-fold increase at 7 days, p < 0.01), superoxide dismutase 1 (1.494-fold increase at 7 days, p < 0.05), and NAD(P)H: quinone oxidoreduate-1 (1.376-fold increase at 7 days, p < 0.05) in obstructed kidneys. Collectively, these findings suggest that inhibiting DNA methylation restores the disrupted balance between pro-inflammatory and anti-inflammatory pathways to alleviate renal inflammation and fibrosis. Therefore, these results highlight the possibility of DNA methyltransferases as therapeutic targets for treating renal inflammation and fibrosis.

Original languageEnglish
Article number14045
JournalInternational Journal of Molecular Sciences
Volume23
Issue number22
DOIs
StatePublished - Nov 2022

Bibliographical note

Funding Information:
This research was supported by the Basic Science Research Program (NRF-2017R1D1A1B03031133 to E.S.K.; NRF-2017R1D1A1B03035813 to S.J.S.) and a grant (2019R1A5A2027588 to H.-S.K.) through the National Research Foundation of Korea, which is funded by the Ministry of Science, ICT & Future Planning, in the Republic of Korea. This research was also supported through the 2016 grant of the Institute of Clinical Medicine Research in the Yeouido St. Mary’s Hospital, a grant of the Translational R&D Project through the Institute for Bio-Medical convergence, Incheon St. Mary’s Hospital, at the Catholic University of Korea, and a grant from Catholic Alumni of Nephrologist.

Publisher Copyright:
© 2022 by the authors.

Keywords

  • DNA methyltransferase
  • fibrosis
  • inflammation
  • oxidative stress
  • unilateral ureteral obstruction

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