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400016 重庆,重庆医科大学附属第一医院眼科,眼科学重庆市市级重点实验室,重庆市眼科研究所
[彭惠,E-mail: pengh9@sina.comPENG Hui, E-mail: pengh9@sina.com
收稿:2022-04-05,
修回:2022-06-13,
纸质出版:2022-11-15
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陈金泉, 赵龙, 丁渲恒, 等. 川芎嗪通过调控NRF2/HO-1途径抑制高糖诱导的中性粒细胞外捕获网形成[J]. 陆军军医大学学报, 2022,44(21):2157-2164.
Jinquan CHEN, Long ZHAO, Xuanheng DING, et al. Tetramethylpyrazine inhibits NETs formation induced by high glucose by regulating NRF2/HO-1 pathway[J]. Journal of Army Medical University, 2022, 44(21): 2157-2164.
陈金泉, 赵龙, 丁渲恒, 等. 川芎嗪通过调控NRF2/HO-1途径抑制高糖诱导的中性粒细胞外捕获网形成[J]. 陆军军医大学学报, 2022,44(21):2157-2164. DOI: 10.16016/j.2097-0927.202204038.
Jinquan CHEN, Long ZHAO, Xuanheng DING, et al. Tetramethylpyrazine inhibits NETs formation induced by high glucose by regulating NRF2/HO-1 pathway[J]. Journal of Army Medical University, 2022, 44(21): 2157-2164. DOI: 10.16016/j.2097-0927.202204038.
目的
2
探讨川芎嗪(tetramethylpyrazine
TMP)对高糖诱导的中性粒细胞外捕获网(neutrophil extracellular traps
NETs)形成的影响及机制。
方法
2
运用CCK-8检测不同浓度(0、5、10、20、40、80 μmol/L)的TMP处理4 h后中性粒细胞的活性。将中性粒细胞分为7组:Control组(1.5 g/L葡萄糖)、TMP组(40 μmol/L TMP)、HG组(4.5 g/L葡萄糖)、HG+TMP组(40 μmol/L TMP+4.5 g/L葡萄糖)、HG+TMP+ML385组(4.5 g/L葡萄糖+40 μmol/L TMP+10 μmol/L ML385)、HG+ML385组(4.5 g/L葡萄糖+10 μmol/L ML385)和HG+DPI组(4.5 g/L葡萄糖+10 μmol/L DPI)。通过免疫荧光观察NETs的结构;运用DHE和DCFH-DA检测中性粒细胞内ROS和超氧化物阴离子的表达量;采用ELISA试剂盒检测培养基中MPO-DNA的含量,Pico-Green kit试剂盒检测培养基中dsDNA含量,Western blot检测细胞内H3-cit、NRF2、HO-1、NOX2等的表达,评估TMP对NRF2信号级联的调控作用。
结果
2
80 μmol/L的TMP会降低中性
粒细胞活性(
P
<
0.01)
其余浓度的TMP对中性粒细胞活性无显著影响。与Control组比较,TMP组中性粒细胞NRF2、HO-1表达明显上升(
P
<
0.01)。与HG组比较,HG+TMP组中性粒细胞产生的H3-cit表达显著降低(
P
<
0.05),并且培养基中dsDNA和MPO-DNA含量明显下降(
P
<
0.01)。免疫荧光未观察到HG+TMP组中NETs形成;HG+TMP组中性粒细胞产生的ROS和超氧化物阴离子较HG组中性粒细胞显著降低(
P
<
0.01)。使用NRF2抑制剂ML385处理后,TMP对H3-cit、NRF2和HO-1的作用被逆转;培养基中dsDNA和MPO-DNA含量明显上升(
P
<
0.01),并且胞内ROS和超氧化物阴离子相较HG+TMP组的中性粒细胞显著升高(
P
<
0.01)。
结论
2
TMP可以激活NRF2/HO-1通路并抑制ROS的形成,从而抑制高糖诱导的中性粒细胞外捕获网形成。
Objective
2
To investigate the effect and mechanism of tetramethylpyrazine (TMP) on the formation of neutrophil extracellular traps (NETs) induced by high glucose.
Methods
2
The viability of neutrophils treated with TMP of 0
5
10
20
40
and 80 μmol/L for 4 h was measured by CCK-8 assay. Neutrophils were divided into Control group (1.5 g/L glucose)
TMP group (40 μmol/L TMP)
HG group (4.5 g/L glucose)
HG+TMP group (40 μmol/L TMP+4.5 g/L glucose)
HG+TMP+ML385 group (4.5 g/L glucose+40 μmol/L TMP+10 μmol/L ML385)
HG+ML385 group (4.5 g/L glucose+10 μmol/L ML385) and HG+DPI group (4.5 g/L glucose+10 μmol/L DPI). The structure of NETs was observed with immunofluorescence assay. The contents of reactive oxygen species (ROS) and superoxide anions were detected using dichloro-dihydro-fluorescein diacetate (DCFH-DA) assay and dihydroethidine (DHE) method. MPO-DNA and dsDNA in the culture medium was measured with ELISA and Pico-Green kit
respectively. Western blotting was used to detect the intracellular expression of H3-cit
NRF2
HO-1
and NOX2 proteins.
Results
2
TMP of 80 μmol/L had significant effect on neutrophil (
P
<
0.01)
but no such effects were seen in TMP at other doses viability. Compared with the Control group
the expression levels of NRF2 a
nd HO-1 were increased significantly in TMP group (
P
<
0.01)
while that of H3-cit was obviously decreased after TMP treatment (
P
<
0.05)
and the contents of dsDNA and MPO-DNA in the medium were decreased notably (
P
<
0.01). NETs formation was not observed by immunofluorescence assay in the HG+TMP group. The productions of ROS and superoxide anions in the HG+TMP group were significantly lower than those produced in the HG group (
P
<
0.01). The effects of TMP on the expression of H3-cit
NRF2
and HO-1 were reversed after treatment with NRF2 inhibitor ML385. Compared with the HG+TMP group
the contents of dsDNA and MPO-DNA were increased significantly (
P
<
0.01)
and the contents of intracellular ROS and superoxide anions were elevated remarkably in HG+TMP+ML385 group (
P
<
0.01).
Conclusion
2
TMP can activate the NRF2/HO-1 pathway and then suppress the production of ROS
and thus inhibit the NETs formation induced by high glucose.
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