Protective Effects of Peroxiredoxin 6 in Pro-Inflammatory Response Model Using Raw 264.7 Macrophages

---

Svetlana B. Parfenyuk^1,a*, Olga V. Glushkova¹, Mars G. Sharapov¹, Maksim O. Khrenov¹, Sergey M. Lunin¹, Anna A. Kuzekova¹, Elvira K. Mubarakshina¹, Tatyana V. Novoselova¹, Dmitrii A. Cherenkov², and Elena G. Novoselova¹

¹Institute of Cell Biophysics, Pushchino Scientific Center for Biological Research, Russian Academy of Sciences, 142290 Pushchino, Moscow Region, Russia

²Voronezh State University of Engineering Technologies, 394036 Voronezh, Russia

^* To whom correspondence should be addressed.

Received June 5, 2023; Revised July 14, 2023; Accepted July 15, 2023

---

The aim of the work was to study effects of peroxiredoxin 6 (PRDX6), a recombinant antioxidant protein, on the level of pro-inflammatory responses of RAW 264.7 macrophages to endotoxin exposure. Addition of LPS to the RAW 264.7 cell culture medium expectedly increased production of TNF-α, and addition of PRDX6 led to a significant (15-20%) decrease in its production. The level of production of another pro-inflammatory cytokine, IL-1β, which was significantly activated by endotoxin, was completely normalized under the PRDX6 action. Moreover, addition of PRDX6 reduced production of reactive oxygen species (ROS) induced by endotoxin and also prevented overexpression of the iNos gene in the RAW 264.7 cells. The results showed that PRDX6 had a suppressive effect on the expression of Nrf-2 gene and production of the transcription factor NRF-2 during the first 6 h of cell cultivation. Addition of endotoxin caused activation of the NF-κB and SAPK/JNK signaling cascades, while in the presence of PRDX6, activity of these signaling cascades decreases. It is known that the pro-inflammatory response of cells caused by exposure to bacterial LPS leads to activation of apoptosis and elimination of the damaged cells. Our studies confirm this, since exposure to LPS led to activation of the expression of P53 gene, a marker of apoptosis. Peroxiredoxin 6 added within the first hours of the development of acute pro-inflammatory response suppressed the P53 gene expression, indicating protective effect of PRDX6 that reduced apoptosis in the RAW 264.7 macrophages.

---

KEY WORDS: peroxiredoxin 6, inflammation, cytokines, gene expression, signaling cascades

DOI: 10.1134/S0006297923080096

---