Cathepsin B Affects the Activation of Nucleotide-binding Domain and Leucine-rich-repeat-containing Family and Pyrin Domain-containing 3 Inflammasome via Transient Receptor Potential Mucolipin-1.
10.3881/j.issn.1000-503X.10847
- Author:
Juan Juan DUAN
1
;
Qi Fang ZHANG
2
;
Zong Hua HUANG
3
;
Hong Mei ZENG
1
;
Hua BAI
1
Author Information
1. Department of Neurology,the Third Affiliated Hospital in Guizhou Medical University,Tuyun,Guizhou 558000,China.
2. Key Laboratory of Medical Molecular Biology,Guizhou Medical University,Guiyang 550004,China.
3. Department of Clinical Laboratory,the Third Affiliated Hospital in Guizhou Medical University,Tuyun,Guizhou 558000,China.
- Publication Type:Journal Article
- MeSH:
Animals;
Cathepsin B;
antagonists & inhibitors;
metabolism;
Cell Line;
Gene Silencing;
Hydrogen Peroxide;
Inflammasomes;
metabolism;
Interleukin-1beta;
Mice;
Microglia;
NLR Family, Pyrin Domain-Containing 3 Protein;
metabolism;
Oxidative Stress;
Pyrin Domain;
Transient Receptor Potential Channels;
metabolism
- From:
Acta Academiae Medicinae Sinicae
2019;41(2):208-215
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the effects of cathepsin B(CTSB)on the activation of nucleotide-binding domain and leucine-rich-repeat-containing family and pyrin domain-containing 3(NLRP3)inflammasome via transient receptor potential mucolipin-1(TRPML1)in cell oxidative stress model and specific gene silencing cell model. Methods BV2 cells cultured in vivo were treated separately or simultaneously with hydrogen peroxide(HO),calcium-sensitive receptor agonist gadolinium trichloride(GdCl),and CTSB inhibitor CA-074Me,and interleukin-1(IL-1)beta and caspase-1 protein were detected by enzyme-linked immunosorbent assay.The growth activity of BV2 cells in each group was measured by MTT.BV2 cells were treated with different concentrations of HO.Cystatin C mRNA and TRPML1 mRNA in BV2 cells were detected by real-time quantitative polymerase chain reaction and the proteins of TRPML1,CTSB,cathepsin D(CTSD),cathepsin L(CTSL)and cathepsin V(CTSV)were detected by Western blot.Specific small interfering RNA was designed for TRPML1 gene target sequence.TRPML1 gene silencing cell lines(named Tr-si-Bv2 cells)were established in BV2 cells and treated with or without HO.TRPML1,CTSB and transcription factor EB(TFEB)proteins in Tr-si-Bv2 cells or control cells were detected by Western blot. Results After treatment with HO,the expression of caspase-1 protein and NLRP3 mRNA in BV2 cells was increased,and IL-1beta protein in BV2 cells was significantly increased after treatment with GdCl(P=0.0036).After treatment with CA-074Me,the doses of NLRP3 mRNA(P=0.037),caspase-1(P=0.021),and IL-1β(P= 0.036)were significantly reduced.Cells in the HO group and HO+GdCl group grew more slowly.The expressions of CTSB mRNA and TRPML1 mRNA,or CTSB and TRPML1 proteins in BV2 cells in the treatment group with 200 μmol/L of HO concentration were similar.HO-induced CTSB protein expression was inhibited after silencing TRPML1 gene.The changes of other cathepsins were not affected for the different concentration of HO.In the BV2 cells treated with TRPML1 gene silencing,the expression of CTSB protein was significantly reduced and the difference was statistically significant(P=0.021)between the HO +siRNA treatment group and the HO treatment group.Conclusion CTSB regulates the activation of NLRP3 inflammasome in the oxidative stress model of microglia cells,probably mediated by calcium channel protein TRPML1.
