Akt2 inhibitor promotes M2 macrophage polarization in rats with periapical inflammation by reducing miR-155-5p expression.
10.12122/j.issn.1673-4254.2023.04.09
- Author:
Jingyi LI
1
;
Siyuan YANG
1
;
Zhen HAN
1
;
Tianle JIANG
1
;
Yao ZHU
1
;
Zihang ZHOU
1
;
Jingping ZHOU
1
Author Information
1. School of Stomatology/Oral Disease Research Center, Wannan Medical College, Wuhu 241000, China.
- Publication Type:Journal Article
- Keywords:
Akt2;
C/EBPβ;
macrophage polarization;
miR-155-5p;
periapical inflammation
- MeSH:
Rats;
Animals;
Proto-Oncogene Proteins c-akt/metabolism*;
MicroRNAs/genetics*;
Interleukin-10;
Rats, Sprague-Dawley;
Macrophages/metabolism*;
Inflammation/metabolism*
- From:
Journal of Southern Medical University
2023;43(4):568-576
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the effect of Akt2 inhibitor on macrophage polarization in the periapical tissue in a rat model of periapical inflammation.
METHODS:Rat models of periapical inflammation were established in 28 normal SD rats by opening the pulp cavity of the mandibular first molars, followed by injection of normal saline and Akt2 inhibitor into the left and right medullary cavities, respectively. Four rats without any treatment served as the healthy control group. At 7, 14, 21 and 28 days after modeling, 7 rat models and 1 control rat were randomly selected for observation of inflammatory infiltration in the periapical tissues by X-ray and HE staining. Immunohistochemistry was used to detect the expression and localization of Akt2, macrophages and the inflammatory mediators. RT-PCR was performed to detect the mRNA expressions of Akt2, CD86, CD163, inflammatory mediators, miR-155-5p and C/EBPβ to analyze the changes in macrophage polarization.
RESULTS:X-ray and HE staining showed that periapical inflammation was the most obvious at 21 days after modeling in the rats. Immunohistochemistry and RT-PCR showed that compared with those in the control rats, the expressions of Akt2, CD86, CD163, miR-155-5p, C/EBPβ, and IL-10 increased significantly in the rat models at 21 days (P < 0.05). Compared with saline treatment, treatment with the Akt2 inhibitor significantly decreased the expression levels of Akt2, CD86, miR-155-5p and IL-6 and the ratio of CD86+M1/CD163+M2 macrophages (P < 0.05) and increased the expression levels of CD163, C/EBPβ and IL-10 in the rat models (P < 0.05).
CONCLUSION:Inhibition of Akt2 can delay the progression of periapical inflammation in rats and promote M2 macrophage polarization in the periapical inflammatory microenvironment possibly by reducing miR-155-5p expression and activating the expression of C/EBPβ in the Akt signaling pathway.
