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Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism

  • Authors:
    • Yuehui Zhang
    • Wenhui Su
    • Yaoyun Niu
    • Hongli Zeng
    • Lu Liu
    • Lijun Wang
    • Weidong Xie
  • View Affiliations / Copyright

    Affiliations: Department of Critical Care Medicine, The Second Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong 518101, P.R. China, State Key Laboratory of Chemical Oncogenomics, Institute of Biopharmaceutical and Health Engineering, Shenzhen International Graduate School, Tsinghua University, Shenzhen, Guangdong 518055, P.R. China
    Copyright: © Zhang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 67
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    Published online on: March 1, 2024
       https://doi.org/10.3892/mmr.2024.13191
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Abstract

Inflammasome activation is a crucial mechanism in inflammatory responses. Bax‑interacting factor 1 (Bif‑1) is required for the normal formation of autophagosomes, but its ability to exert an inflammatory regulatory effect remains unclear. The aim of the present study was to explore the role of Bif‑1 in inflammation, possibly mediated through autophagy regulation. Using a lipopolysaccharide (LPS)/adenosine triphosphate (ATP)‑induced inflammatory model in J774A.1 cells, the effect of Bif‑1 on inflammasome activation and the underlying mechanisms involving autophagy regulation were investigated. Elevated levels of NLR family pyrin domain containing protein 3 inflammasome and interleukin‑1β (IL‑1β) proteins were observed in J774A.1 cells after LPS/ATP induction. Furthermore, Bif‑1 and autophagy activity were significantly upregulated in inflammatory cells. Inhibition of autophagy resulted in inflammasome activation. Silencing Bif‑1 expression significantly upregulated IL‑1β levels and inhibited autophagy activity, suggesting a potential anti‑inflammatory role of Bif‑1 mediated by autophagy. Additionally, inhibition of the nuclear factor‑κB (NF‑κB) signaling pathway downregulated Bif‑1 and inhibited autophagy activity, highlighting the importance of NF‑κB in the regulation of Bif‑1 and autophagy. In summary, the current study revealed that Bif‑1 is a critical anti‑inflammatory factor against inflammasome activation mediated by a mechanism of autophagy regulation, indicating its potential as a therapeutic target for inflammatory regulation.
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Spandidos Publications style
Zhang Y, Su W, Niu Y, Zeng H, Liu L, Wang L and Xie W: Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism. Mol Med Rep 29: 67, 2024.
APA
Zhang, Y., Su, W., Niu, Y., Zeng, H., Liu, L., Wang, L., & Xie, W. (2024). Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism. Molecular Medicine Reports, 29, 67. https://doi.org/10.3892/mmr.2024.13191
MLA
Zhang, Y., Su, W., Niu, Y., Zeng, H., Liu, L., Wang, L., Xie, W."Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism". Molecular Medicine Reports 29.4 (2024): 67.
Chicago
Zhang, Y., Su, W., Niu, Y., Zeng, H., Liu, L., Wang, L., Xie, W."Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism". Molecular Medicine Reports 29, no. 4 (2024): 67. https://doi.org/10.3892/mmr.2024.13191
Copy and paste a formatted citation
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Spandidos Publications style
Zhang Y, Su W, Niu Y, Zeng H, Liu L, Wang L and Xie W: Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism. Mol Med Rep 29: 67, 2024.
APA
Zhang, Y., Su, W., Niu, Y., Zeng, H., Liu, L., Wang, L., & Xie, W. (2024). Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism. Molecular Medicine Reports, 29, 67. https://doi.org/10.3892/mmr.2024.13191
MLA
Zhang, Y., Su, W., Niu, Y., Zeng, H., Liu, L., Wang, L., Xie, W."Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism". Molecular Medicine Reports 29.4 (2024): 67.
Chicago
Zhang, Y., Su, W., Niu, Y., Zeng, H., Liu, L., Wang, L., Xie, W."Bif‑1 inhibits activation of inflammasome through autophagy regulatory mechanism". Molecular Medicine Reports 29, no. 4 (2024): 67. https://doi.org/10.3892/mmr.2024.13191
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