Effect of Baicalin on Pyroptosis of Diffuse Large B-Cell Lymphoma Cell Lines DB and Its Mechanism.
10.19746/j.cnki.issn.1009-2137.2023.06.016
- Author:
Ming LU
1
;
Chun-Ling HE
1
;
Zhen-Tian WU
2
;
Yao LYU
2
;
Xiao-Hui DUAN
2
;
Bing-Xuan WANG
2
;
Shi-Xiong WANG
2
;
Jian-Hong WANG
2
;
Rong LIANG
3
Author Information
1. The Second Clinical Medical College of Shaanxi University of Chinese Medicine, Xi'an 712046, Shanxi Province, China.
2. Department of Hematology, The First Affiliated Hospital of Air Force Military Medical University, Xi'an 710032, Shaanxi Province, China.
3. Department of Hematology, The First Affiliated Hospital of Air Force Military Medical University, Xi'an 710032, Shaanxi Province, China,E-mail: rongliang1017@gmail.com.
- Publication Type:Journal Article
- Keywords:
NLRP3;
ROS;
baicalin;
diffuse large B cell Lymphoma;
pyroptosis
- MeSH:
Humans;
NLR Family, Pyrin Domain-Containing 3 Protein/metabolism*;
Reactive Oxygen Species/pharmacology*;
Pyroptosis;
Cell Line;
RNA, Messenger;
Lymphoma, Large B-Cell, Diffuse
- From:
Journal of Experimental Hematology
2023;31(6):1706-1713
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the effect of Baicalin on the proliferation and pyroptosis of diffuse large B-cell lymphoma cell line DB and its mechanism.
METHODS:DB cells were treated with baicalin at different concentrations (0, 5, 10, 20, 40 μmol/L). Cell proliferation was detected by CCK-8 assay and half maximal inhibitory concentration (IC50) was calculated. The morphology of pyroptosis was observed under an inverted microscope, the integrity of the cell membrane was verified by LDH content release assay, and the expressions of pyroptosis-related mRNA and protein (NLRP3, GSDMD, GSDME, N-GSDMD, N-GSDME) were detected by real-time fluorescence quantitative PCR and Western blot. In order to further clarify the relationship between baicalin-induced pyroptosis and ROS production in DB cells, DB cells were divided into control group, baicalin group, NAC group and NAC combined with baicalin group. DB cells in the NAC group were pretreated with ROS inhibitor N-acetylcysteine (NAC) 2 mmol/L for 2 h. Baicalin was added to the combined treatment group after pretreatment, and the content of reactive oxygen species (ROS) in the cells was detected by DCFH-DA method after 48 hours of culture.
RESULTS:Baicalin inhibited the proliferation of DB cells in a dose-dependent manner (r=-0.99), and the IC50 was 20.56 μmol/L at 48 h. The morphological changes of pyroptosis in DB cells were observed under inverted microscope. Compared with the control group, the release of LDH in the baicalin group was significantly increased (P<0.01), indicating the loss of cell membrane integrity. Baicalin dose-dependently increased the expression levels of NLRP3, N-GSDMD, and N-GSDME mRNA and protein in the pyroptosis pathway (P<0.05). Compared with the control group, the level of ROS in the baicalin group was significantly increased (P<0.05), and the content of ROS in the NAC group was significantly decreased (P<0.05). Compared with the NAC group, the content of ROS in the NAC + baicalin group was increased. Baicalin significantly attenuated the inhibitory effect of NAC on ROS production (P<0.05). Similarly, Western blot results showed that compared with the control group, the expression levels of pyroptosis-related proteins was increased in the baicalin group (P<0.05). NAC inhibited the expression of NLRP3 and reduced the cleavage of N-GSDMD and N-GSDME (P<0.05). Compared with the NAC group, the NAC + baicalin group had significantly increased expression of pyroptosis-related proteins. These results indicate that baicalin can effectively induce pyroptosis in DB cells and reverse the inhibitory effect of NAC on ROS production.
CONCLUSION:Baicalin can inhibit the proliferation of DLBCL cell line DB, and its mechanism may be through regulating ROS production to affect the pyroptosis pathway.
