独活寄生汤调控衣霉素诱导的内质网应激减缓人髓核细胞凋亡OA北大核心CSTPCD
Duhuo Jisheng decoction reduces apoptosis of human nucleus pulposus cells by regulating tunicamycin-induced endoplasmic reticulum stress
目的:研究独活寄生汤对衣霉素诱导的人髓核细胞内质网应激和细胞凋亡的作用及机制.方法:将30只10周龄的SD大鼠以独活寄生汤灌胃,连续灌胃14 d后经腹主动脉取血,获取含药血清.采用衣霉素和不同浓度独活寄生汤处理人髓核细胞,使用CCK-8检测髓核细胞的活力.将人髓核细胞随机分为5组:对照组(未经衣霉素和独活寄生汤含药血清处理),衣霉素组(加入10 μg/mL 衣霉素溶液),衣霉素+4-PBA组(加入10 μg/mL衣霉素溶液和5 mmol/mL 4-PBA),衣霉素+独活寄生汤组(加入10 μg/mL衣霉素溶液和10%独活寄生汤含药血清),衣霉素+生理盐水组(加入10 μg/mL衣霉素溶液和等剂量生理盐水).免疫荧光法检测各组CHOP、GRP78的表达水平;TUNEL法检测分析髓核细胞凋亡率;qRT-PCR法和Western Blot法分别检测各组CHOP、GRP78、内质网应激和凋亡相关通路 mRNA和蛋白的表达.结果:独活寄生汤能够增强髓核细胞活力、降低髓核细胞凋亡率,对衣霉素可能存在拮抗作用.与对照组相比,衣霉素处理后髓核细胞中CHOP、GRP78、Cleaved-caspase3、Bax和PERK/elF2α、IREI/JNK和Caspase12等凋亡相关通路的蛋白和基因表达显著升高,BCL-2蛋白和基因表达显著下降,差异有统计学意义(P<0.05);而衣霉素+生理盐水组表达与衣霉素组相当,差异无统计学意义.与衣霉素组相比,衣霉素+独活寄生汤含药血清组中的CHOP、GRP78、Cleaved-caspase3、Bax和PERK/elF2α、IREI/JNK和Caspase12等凋亡相关通路的蛋白和基因表达出现明显下降,BCL-2蛋白和基因表达显著升高,差异有统计学意义(P<0.05);其调控效果与阳性对照衣霉素+4-PBA组相当,差异无统计学意义.结论:衣霉素能够诱导髓核细胞内质网应激,促使细胞凋亡增加;独活寄生汤对衣霉素诱导的内质网应激具有调控作用,抑制髓核细胞凋亡,从而延缓椎间盘退变.
Objective:To study the effect and mechanism of Duhuo Jisheng decoction on endoplasmic reticulum stress and apoptosis of human nucleus pulposus cells induced by tunicamycin.Methods:Thirty SD rats of 10 weeks old were gavaged with Duhuo Jisheng decoction,and blood samples were collected through abdominal aorta after 14 days.Human nucleus pulposus cells were treated with tunicamycin and different concentrations of Duhuo Jisheng decoction,and CCK-8 was used to detect the activity of nucleus pulposus cells.Human nucleus pulposus cells were randomly divided into five groups:the Control group(not treated with tunicamycin and Duhuo Jisheng decoction-containing serum),the tunicamycin group(adding 10 μg/mL tunicamycin solu-tion),the tunicamycin+4-PBA group(adding 10 μg/mL tunicamycin solution and 5 mmol/mL 4-PBA),the tunicamycin+Duhuo Jisheng decoction group(adding 10 μg/mL tunicamycin solution and 10%medicated serum of Duhuo Jisheng decoction),the tunicamycin+normal saline group(adding 10 μg/mL tunicamycin solution and equal dose of normal saline).The expression levels of CHOP and GRP78 were detected by immunofluorescence.The apoptosis rate of nucleus pulposus cells was detected by TUNEL.The mRNA and protein expressions of CHOP,GRP78,endoplasmic reticulum stress and apoptosis-related pathways were detected by qRT-PCR and Western Blot,respectively.Results:Duhuo Jisheng decoction could enhance the activity of nucle-us pulposus cells,decrease the apoptosis rate of nucleus pulposus cells,and may have antagonistic effect on tunicamycin.Com-pared with the control group,protein and gene expressions of CHOP,GRP78,Cleaved-caspase3,Bax and apoptosis-related path-ways such as PERK/elF2α,IREI/JNK and Caspase12 were significantly increased after tunicamycin treatment,while protein and gene expressions of BCL-2 were significantly decreased.The difference was statistically significant(P<0.05).The expression of tunicamycin+saline group was similar to that of tunicamycin group,and the difference was not statistically significant.Protein and gene expressions of CHOP,GRP78,Cleaved-caspase3,Bax and apoptosis-related pathways such as PERK/elF2α,IREI/JNK and Caspase12,were significantly decreased in the tunicamycin+Duhuo jisheng decoction-containing serum group com-pared with the tunicamycin group.The expression of BCL-2 protein and gene was significantly increased,with statistical signifi-cance(P<0.05).The regulatory effect was similar to that of the positive control group,tunicamycin+4-PBA,and the difference was not statistically significant.Conclusion:Tunicamycin can induce endoplasmic reticulum stress in nucleus pulposus cells and promote apoptosis.Duhuo Jisheng decoction can regulate the tunicamycin-induced endoplasmic reticulum stress,inhibit the apopto-sis of nucleus pulposus cells,and delay the degeneration of intervertebral disc.
李艳丽;杨若鹏;夏平
湖北中医药大学,湖北 武汉 430065
中医学
髓核细胞椎间盘退变内质网应激衣霉素
Nucleus pulposus apoptosisIntervertebral disc degenerationEndoplasmic reticulum stressTunicamycin
《海南医学院学报》 2024 (012)
913-920,929 / 9
This study was supported by Project of Wuhan Health and Family Planning Commission(WX21M02,WZ21C04)武汉市卫计委项目(WX21M02,WZ21C04)
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