已发表论文

缺氧和脂多糖通过 PKR-p-eIF2α 通路和 4EBP1 通路诱导的应激颗粒聚集抑制种植体周围炎的炎症反应

 

Authors Li S, Ma C, Fan C, Liu Y, Li J, Yin B, Zhong L, Bai N, Li Z

Received 19 February 2025

Accepted for publication 26 July 2025

Published 4 August 2025 Volume 2025:18 Pages 10533—10544

DOI https://doi.org/10.2147/JIR.S523799

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Renan Dal Fabbro

Shuang Li,1,2,* Chunling Ma,3,* Chun Fan,4 Yanshan Liu,5 Jian Li,2,6 Baoheng Yin,1,2 Lingmei Zhong,7 Na Bai,1,2 Zhiyuan Li3 

1Department of Prosthodontics, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, People’s Republic of China; 2School of Stomatology, Qingdao University, Qingdao, Shandong, People’s Republic of China; 3Medical Research Center, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, People’s Republic of China; 4Department of Periodontology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, People’s Republic of China; 5Department of Maxillofacial Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, People’s Republic of China; 6Department of Oral Implantology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, People’s Republic of China; 7Department of Pulmonary and Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Zhiyuan Li, Email zyli0120@163.com Na Bai, Email na.bai@qdu.edu.cn

Objective: To investigate whether stress granules (SGs) exist in peri-implantitis (PI) and to explore the formation mechanism and role of SGs in the response of human gingival fibroblasts (hGFs) to hypoxia or LPS.
Methods: Gingival tissues were collected from patients with PI and from healthy individuals. RT-qPCR, Western blotting, and immunofluorescence staining were used to detect the SGs in the gingiva. Healthy hGFs were cultured and the activation of SGs in LPS- or hypoxia-treated hGFs was evaluated. Knockdown assays using siRNAs were performed to investigate the formation mechanism and the role of SGs in hGFs.
Results: SGs aggregates were present in gingival tissues of patients with PI. LPS or hypoxia stimulation induces SGs formation and leads to eIF2α phosphorylation and 4EBP1 hypophosphorylation in hGFs. Knockdown of PKR or 4EBP1 decreases the number of SGs in stressed hGFs and enhances LPS- and hypoxia-induced TNF-α and IL-1β expression.
Conclusion: Our study revealed SGs aggregation in the PI gingiva. Hypoxia and LPS can induce SGs assembly in hGFs in vitro via PKR-p-eIF2α and 4EBP1 pathways. SGs in hGFs exert a protective effect against inflammatory responses, suggesting their role in balancing pro- and anti-inflammatory responses, thus providing a new approach for protecting against destructive inflammatory responses.
Plain Language Summary: Hypoxia and Porphyromonas gingivalis-LPS induced SGs assembly in hGFs via the PKR-p-eIF2α and 4EBP1 pathways, whereas SGs exerted a protective effect against hypoxia and P. gingivalis-LPS-induced inflammatory response.

Keywords: peri-implantitis, stress granules, hypoxia, LPS