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Publishing Language: Chinese

TUDCA promotes intracellular clearance of Burkholderia pseudomallei by inhibiting endoplasmic reticulum stress-induced apoptosis in RAW264.7 cells

Guangqiang ZHAO1Dongqi NAN2Siqi YUAN2Chenglong RAO2Zhenquan XING1Bin WANG1Yao FANG3Xuhu MAO2,4Qian LI2,4( )
Department of Respiratory Diseases, Sanya People's Hospital (West China Sanya Hospital, Sichuan University), Sanya, Hainan Province, 572022
Department of Clinical Microbiology and Immunology, Faculty of Pharmacy and Medical Laboratory, Army Medical University (Third Military Medical University), Chongqing, 400038
Department of Respiratory and Critical Care Medicine, General Hospital of Center Theater of PLA, Wuhan, Hubei Province, 430070, China
State Key Laboratory of Trauma and Chemical Poisoning, Army Medical University (Third Military Medical University), Chongqing, 400038
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Abstract

Objective

To explore the action mechanism of tauroursodeoxycholic acid (TUDCA) promoting intracellular clearance of Burkholderia pseudomallei (B. pseudomallei) in RAW264.7 macrophages.

Methods

After TUDCA of different concentrations were used to treat RAW264.7 cells pre-infected with B. pseudomallei for 8 h or not, flow cytometry was applied to detect the apoptosis of the infected and control cells. In addition, another endoplasmic reticulum stress (ERS) inhibitor 4-PBA was used to detect the apoptosis and proliferation of host cells after B. pseudomallei infection with Annexin-V/PI double staining and MTT cell proliferation assay. Furthermore, after transfected with CHOP siRNA, Western blotting and flow cytometry were employed to detect the effect of TUDCA on the expression levels of Caspase-3 and Caspase-12 and the changes in apoptotic rate after B. pseudomallei infection, respectively. Finally, the effect of TUDCA on intracellular multiplication of infected RAW264.7 cells were observed to estimate the CFU value in the presence and absence of CHOP siRNA.

Results

Under different concentrations of TUDCA, 100 or 200 μmol/L TUDCA significantly reduced B. pseudomallei-induced apoptosis in RAW264.7 cells (P < 0.05). Meanwhile, both TUDCA and 4-PBA treatment could decrease the apoptosis induced by B. pseudomallei infection by ERS (P < 0.05). Further, the expression levels of Caspase-3 and Caspase-12 were obviously increased after B. pseudomallei infection compared with uninfected groups, but their expression levels in the siCHOP group was significantly lower than that in the siC group. Besides, flow cytometry also showed that TUDCA could reduce apoptosis induced by B. pseudomallei infection (P < 0.05), but no significant effect of TUDCA on apoptosis was observed under CHOP knockdown. Finally, intracellular CFU assay indicated that TUDCA treatment promoted the host cell clearance of B. pseudomallei (P < 0.05), but no such effect was observed in siCHOP group.

Conclusion

In B. pseudomallei infected RAW264.7 cells, TUDCA promotes the intracellular clearance of the bacteria by inhibiting ERS-induced apoptosis.

CLC number: R285.5;R329.28;R378.99 Document code: A

References

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Journal of Army Medical University
Pages 225-231

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Cite this article:
ZHAO G, NAN D, YUAN S, et al. TUDCA promotes intracellular clearance of Burkholderia pseudomallei by inhibiting endoplasmic reticulum stress-induced apoptosis in RAW264.7 cells. Journal of Army Medical University, 2024, 46(3): 225-231. https://doi.org/10.16016/j.2097-0927.202304046

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Received: 11 April 2023
Revised: 14 September 2023
Published: 15 February 2024
© 2024 Journal of Army Medical University