TUDCA promotes intracellular clearance of Burkholderia pseudomallei by inhibiting endoplasmic reticulum stress-induced apoptosis in RAW264.7 cells
Basic Medicine|更新时间:2026-01-09
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TUDCA promotes intracellular clearance of Burkholderia pseudomallei by inhibiting endoplasmic reticulum stress-induced apoptosis in RAW264.7 cells
Journal of Army Medical UniversityVol. 46, Issue 3, Pages: 225-231(2024)
作者机构:
1.572022 海南 三亚,三亚市人民医院(四川大学华西三亚医院)呼吸内科
2.400038 重庆,陆军军医大学(第三军医大学)药学与检验医学系临床微生物与免疫学教研室
3.430070 武汉,解放军中部战区总医院呼吸与危重症医学科
4.400038 重庆,陆军军医大学(第三军医大学)创伤与化学中毒全国重点实验室
作者简介:
基金信息:
the General Program of National Natural Science Foundation of China(32270190);the General Program of Natural Science Foundation of Hainan Province(821MS162)
Guangqiang ZHAO, Dongqi NAN, Siqi YUAN, et al. TUDCA promotes intracellular clearance of Burkholderia pseudomallei by inhibiting endoplasmic reticulum stress-induced apoptosis in RAW264.7 cells[J]. Journal of Army Medical University, 2024, 46(3): 225-231.
DOI:
Guangqiang ZHAO, Dongqi NAN, Siqi YUAN, et al. TUDCA promotes intracellular clearance of Burkholderia pseudomallei by inhibiting endoplasmic reticulum stress-induced apoptosis in RAW264.7 cells[J]. Journal of Army Medical University, 2024, 46(3): 225-231. DOI: 10.16016/j.2097-0927.202304046.
TUDCA promotes intracellular clearance of Burkholderia pseudomallei by inhibiting endoplasmic reticulum stress-induced apoptosis in RAW264.7 cells
To explore the action mechanism of tauroursodeoxycholic acid (TUDCA) promoting intracellular clearance of
Burkholderia pseudomallei
(
B. pseudomallei
) in RAW264.7 macrophages.
Methods
2
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
2
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
2
In
B. pseudomallei
infected RAW264.7 cells
TUDCA promotes the intracellular clearance of the bacteria by inhibiting ERS-induced apoptosis.
关键词
Keywords
references
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