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慢性阻塞性肺疾病急性加重期患者血清对PM2.5所致MH-S细胞炎症的影响及salubrinal的作用

Effects of chronic obstructive pulmonary disease patients’ serum and salubrinal on inflammation of MH-S cells induced by PM2.5

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【作者】 王正郝赫莉王晓彤武思羽阎锡新张霄鹏孟爱宏

【Author】 WANG Zheng;HAO He-li;WANG Xiao-tong;WU Si-yu;YAN Xi-xin;ZHANGXiao-peng;MENG Ai-hong;Department of Respiratory and Critical Care Medicine,North Ward,The Second Hospital of Hebei Medical University;First Department of Respiratory and Critical Care Medicine,The Second Hospital of Hebei Medical University;Second Department of Thoracic Surgery,Hebei Provincial People’s Hospital;

【通讯作者】 孟爱宏;

【机构】 河北医科大学第二医院北院区呼吸与危重症医学科河北医科大学第二医院呼吸与危重症医学一科河北省人民医院胸外二科

【摘要】 目的:探讨慢性阻塞性肺疾病急性加重期(AECOPD)患者血清和salubrinal在细颗粒物(PM2.5)诱导的小鼠肺泡巨噬细胞株MH-S炎症中的作用。方法:(1)将MH-S细胞分为对照组、PM2.5组、AECOPD患者血清组、健康志愿者血清组、PM2.5+AECOPD患者血清组和PM2.5+健康志愿者血清组,检测组蛋白脱乙酰酶2(HDAC2)活性,细胞上清液中白细胞介素17(IL-17)浓度,分析IL-17与HDAC2活性间的相关性;(2)进一步探究salubrinal对PM2.5刺激的MH-S细胞的作用,分为对照组、PM2.5组和salubrinal+PM2.5组,检测MH-S细胞中C/EBP同源蛋白(CHOP)和葡萄糖调节蛋白78(GRP78)表达、HDAC2活性及细胞上清液中IL-17浓度。结果:(1)PM2.5组、AECOPD患者血清组、健康志愿者血清组和PM2.5+AECOPD患者血清组和PM2.5+健康志愿者血清组较对照组MH-S细胞HDAC2活性均降低,IL-17分泌增加,且AECOPD患者血清组较健康志愿者血清组IL-17升高,MH-S细胞HDAC2活性降低更明显(P<0.05)。PM2.5+AECOPD患者血清组较PM2.5+健康志愿者血清组IL-17升高、HDAC2活性降低明显(P<0.05)。IL-17与HDAC2之间存在负相关(r=-0.786,P<0.01);(2)PM2.5刺激12 h后细胞较对照组CHOP荧光增强、核内居多,GRP78荧光增强、胞质明显,IL-17含量增加,HDAC2活性降低(P<0.05)。加入salubrinal干预后CHOP荧光较PM2.5组减弱,GRP78荧光较PM2.5组增强,IL-17含量降低,HDAC2活性增加(P<0.05)。结论:PM2.5刺激会导致MH-S细胞IL-17分泌增多,HDAC2活性降低,血清会加重PM2.5对MH-S细胞的影响;IL-17与HDAC2之间存在负相关;PM2.5刺激使CHOP和GRP78表达增多,激活MH-S细胞内质网应激;salubrinal可能通过下调MH-S细胞CHOP表达抑制了PM2.5对MH-S细胞炎症功能。

【Abstract】 AIM:To investigate the role of acute exacerbation of chronic obstructive pulmonary disease(AECOPD)patients’ serum and salubrinal in PM2. 5-induced inflammatory function of mouse alveolar macrophages(MHS cells).METHODS:Six groups were set up:control group,PM2. 5 group,AECOPD serum group,healthy volunteer serum group,PM2. 5+AECOPD serum group,and PM2. 5+healthy volunteer serum group. The activity of histone deacetylase 2(HDAC2)and the concentration of interleukin-17(IL-17)in the supernatant of MH-S cells were measured. The correlation between IL-17 and HDAC2 activity was analyzed by Pearson correlation analysis. To further explore the effect of salubrinal on MH-S cell stimulated by PM2. 5,the cells were divided into control group,PM2. 5 group and salubrinal+PM2. 5 group,and stimulated for 12 h. The expression of C/EBP homologus protein(CHOP)and glucose-regulated protein 78(GRP78),the activity of HDAC2 and the concentration of IL-17 in the supernatant were measured.RESULTS:Compared with control group,the activity of HDAC2 was decreased and the secretion of IL-17 was increased in experimental group. The IL-17 concentration were higher and the HDAC2 activity were lower in PM2. 5 and AECOPD serum group compared with PM2. 5 and healthy volunteer serum group(P<0. 05). There was a negative correlation between IL-17 and HDAC2(r=-0. 786,P<0. 01). After stimulation with PM2. 5 for 12 h,the CHOP fluorescence was increased and enter into nucleus obviously,the GRP78 fluorescence was increased and significantly in cytoplasm,the IL-17 content was increased and the HDAC2 activity was decreased compared with control group(P<0. 05). After the intervention of salubrinal,the fluorescence of CHOP was lower than that of PM2. 5,the fluorescence of GRP78 was higher than that of PM2. 5,the content of IL-17 was decreased,and the activity of HDAC2 was increased. The differences were statistically significant(P<0. 05).CONCLUSION:PM2. 5 increases the secretion of IL-17 and decreases the activity of HDAC2 in MH-S cells. Serum aggravates the effect of PM2. 5 on MH-S cells. There is a negative correlation between IL-17 and HDAC2.PM2. 5 stimulation increases the expression of CHOP and GRP78,and activates the endoplasmic reticulum stress. Salubrinal may inhibit the inflammatory effect of PM2. 5 on MH-S cells by inhibiting the expression of CHOP.

【基金】 河北省自然科学基金资助项目(No.H2019206263);河北省应用基础研究计划重点基础研究项目(No.15967753D;No.19277760D);2020年河北省财政厅老年病防治项目
  • 【文献出处】 中国病理生理杂志 ,Chinese Journal of Pathophysiology , 编辑部邮箱 ,2021年07期
  • 【分类号】R563.9
  • 【被引频次】2
  • 【下载频次】185
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