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西格玛 - 1 受体通过 AMPK/mTOR 信号通路在脓毒症诱导的急性肾损伤中恢复自噬

 

Authors Jiang W , Zhang J, Zhang Y, Huang Z

Received 14 November 2024

Accepted for publication 1 February 2025

Published 4 April 2025 Volume 2025:18 Pages 1917—1931

DOI https://doi.org/10.2147/IJGM.S506593

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Sandul Yasobant

Wei Jiang,1 Jianfeng Zhang,2 Yinan Zhang,3 Zhongwei Huang1 

1Department of Emergency Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, 226001, People’s Republic of China; 2Department of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, Jiangsu, 226001, People’s Republic of China; 3Department of Dermatology, Affiliated Hospital of Nantong University, Nantong, Jiangsu, 226001, People’s Republic of China

Correspondence: Zhongwei Huang, Department of Emergency Medicine, Affiliated Hospital of Nantong University, 20 Xisi Road, Nantong, Jiangsu, 226001, People’s Republic of China, Email hzw889@163.com

Purpose: This study aimed to investigate the effects of σ-1R on autophagy in sepsis-AKI and its potential involvement in the AMPK/mTOR signaling pathway.
Methods: The serum samples from patients were used to diagnose sepsis and sepsis-AKI using double-blind and randomized method and to quantify σ-1R and inflammatory cytokines using enzyme-linked immunosorbent assays. HK-2 cells induced by lipopolysaccharide (LPS) were employed as an in vitro model of sepsis-AKI. To evaluate the function of σ-1R in sepsis-AKI, siRNA and an overexpression plasmid targeting σ-1R were used. σ-1R and autophagy marker expressions were analyzed using quantitative real-time polymerase chain reaction and Western blot assays. Cell proliferation was evaluated using CCK-8 and EdU assays, and cell apoptosis was detected using flow cytometry and TUNEL staining assays. Phosphorylated proteins were detected in the AMPK/mTOR signaling pathway.
Results: In sepsis and sepsis-AKI, σ-1R levels were reduced, whereas the levels of interleukin-1β (IL-1β), IL-6, and tumor necrosis factor-α (TNF-α) increased. σ-1R promoted the proliferation of LPS-induced HK-2 cells while inhibiting apoptosis. Moreover, σ-1R enhanced autophagy, as evidenced by the upregulation of autophagy biomarkers LC3-II/LC3-I and Beclin 1. Furthermore, σ-1R promoted the phosphorylation of AMPK and ULK1 while inhibiting mTOR.
Conclusion: σ-1R utilizes the AMPK/mTOR signaling pathway to enhance autophagy in sepsis-AKI, indicating that σ-1R may serve as a promising target for sepsis-AKI diagnosis and therapy.

Keywords: sepsis-induced acute kidney injury, sigma-1 receptor, autophagy, AMPK/mTOR signaling pathway