Type III secretory protein SINC of Chlamydia psittaci promotes host cell autophagy by activating the MAPK/ERK signaling pathway.
10.12122/j.issn.1673-4254.2023.02.19
- Author:
Xin Ding ZENG
1
;
Li CHEN
1
;
Peng ZHOU
1
;
Ting TANG
1
;
Xi CHEN
1
;
Dan HU
1
;
Chuan WANG
2
;
Li Li CHEN
1
Author Information
1. Department of Public Health Laboratory Sciences, School of Public Health, University of South China, Hengyang 421001, China.
2. Institute of Pathogen Biology, Hengyang Medical School, University of South China, Hengyang 421001, China.
- Publication Type:Journal Article
- Keywords:
Chlamydophila psittaci;
MAPK/ERK signaling Pathway;
SINC;
autophagy
- MeSH:
MAP Kinase Signaling System;
Chlamydophila psittaci;
Beclin-1;
Signal Transduction;
Autophagy
- From:
Journal of Southern Medical University
2023;43(2):294-299
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the effects of SINC, a secreted protein of Chlamydia psittaci, on autophagy of host cells and the role of MAPK/ERK signaling pathway in mediating SINC-induced autophagy.
METHODS:RAW 264.7 cells treated with recombinant SINC were examined for changes in expression levels of LC3-II, Beclin-1, phosphorylated and total ERK1/2 using Western blotting. The expression level of LC3 in the treated cells was detected using immunofluorescence analysis, and the formation of autophagosomes and autolysosomes was observed with transmission electron microscopy (TEM). The effect of pretreatment with U0126 (a specific ERK inhibitor) on the expression levels of LC3-II and Beclin-1 in RAW 264.7 cells exposed to different concentrations of SINC was examined using Western blotting, and LC3 puncta in the cells was detected with immunofluorescence analysis.
RESULTS:The expression levels of LC3-II and Beclin-1 were the highest in RAW 264.7 cells treated with 2 μg/mL SINC for 12h. Immunofluorescence analysis showed exposure to SINC significantly increased the number of cells containing LC3 puncta, where the presence of autophagosomes and autolysosomes was detected. Exposure to 2 μg/mL SINC for 15 min resulted in the most significant increase of the ratios of p-ERK1/2/ERK1/2 in RAW 264.7 cells. Pretreatment of the cells with U0126 prior to SINC exposure significantly decreased the ratio of p-ERK1/2/ERK1/2, lowered the expression levels of LC3-II and Beclin-1, and decreased LC3 aggregation in the cells.
CONCLUSIONS:SINC exposure can induce autophagy in RAW 264.7 cells by activating the MAPK/ERK signaling pathway.
