Molecular Immunology2022,Vol.14213.DOI:10.1016/j.molimm.2021.12.012

Activation of TLR4 induces severe acute pancreatitis-associated spleen injury via ROS-disrupted mitophagy pathway

Dong Y. Yang X. Wan C. Chen Z. Yu X. Zhang K. Niu H. Huang W. Wen E. Xin G. Su W. Li S. Zhang Y.
Molecular Immunology2022,Vol.14213.DOI:10.1016/j.molimm.2021.12.012

Activation of TLR4 induces severe acute pancreatitis-associated spleen injury via ROS-disrupted mitophagy pathway

Dong Y. 1Yang X. 2Wan C. 1Chen Z. 1Yu X. 1Zhang K. 1Niu H. 1Huang W. 3Wen E. 3Xin G. 1Su W. 4Li S. 1Zhang Y.5
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作者信息

  • 1. Laboratory of Ethnopharmacology West China School of Medicine West China Hospital Sichuan University
  • 2. Animal Experimental Center of West China Hospital West China Hospital Sichuan University
  • 3. Laboratory of Ethnopharmacology West China School of Pharmacy West China Hospital Sichuan University
  • 4. Department of Neurology of West China Hospital West China Hospital Sichuan University
  • 5. Research Core Facility of West China Hospital West China Hospital Sichuan University
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Abstract

? 2021 Elsevier LtdSevere acute pancreatitis (SAP) is complicated by systemic inflammatory response syndrome and multiple organ dysfunction, the disease will eventually result in death in almost half of the case. The spleen, as the largest immune organ adjacent to the pancreas, is prone to damage in SAP, thereby aggravating the damage of other organs and increasing mortality. However, to date, the research on the mechanism and treatment of spleen injury caused by SAP is still in its infancy. Herein, we investigated the mechanism of spleen injury, and explored the application potential of tuftsin for relieving spleen damage in SAP mice. Firstly, SAP mice model was constructed via the retrograde infusion of 3.5 % sodium taurocholate into the biliopancreatic duct. Then, we proved that the up-regulation of Toll-like receptor 4 (TLR4) in spleen would lead to the accumulation of reactive oxygen species (ROS) and mitochondrial dysfunction under SAP conditions. The splenic ROS and mitochondrial dysfunction could be improved by N-acetylcysteine (NAC) treatment or knocking out TLR4 in SAP mice. Meanwhile, we found that NAC treatment could also improve the autophagy of spleen tissue, suggesting that splenic ROS may affect impaired autophagy, causing the accumulation of damaged mitochondria, aggravating spleen damage. Furthermore, we verified the mechanism of spleen injury is caused by splenic ROS affecting PI3K/p-AKT/mTOR pathway-mediated autophagy. In addition, we detected the spleen injury caused by SAP could decrease the concentration of tuftsin in the serum of mice. Whereas, exogenous supplementation of tuftsin ameliorated the pathological damage, ROS accumulation, impaired autophagy, inflammation expression and apoptosis in damaged spleen. In summary, we verified the new mechanism of SAP-caused spleen damage that TLR4-induced ROS provoked mitophagy impairment and mitochondrial dysfunction in spleen via PI3K/p-AKT mTOR signaling, and the application potential of tuftsin in treating spleen injury, which might expand novel ideas and methods for the treatment of pancreatitis.

Key words

Autophagy/PI3K/AKT/mTOR signaling/ROS/Severe acute pancreatitis/Spleen injury/TLR4

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出版年

2022
Molecular Immunology

Molecular Immunology

ISTP
ISSN:0161-5890
被引量9
参考文献量73
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