首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Co-enzyme Q10 and acetyl salicylic acid enhance Hsp70 expression in primary chicken myocardial cells to protect the cells during heat stress
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Co-enzyme Q10 and acetyl salicylic acid enhance Hsp70 expression in primary chicken myocardial cells to protect the cells during heat stress

机译:共酶Q10和乙酰水杨酸增强初级鸡心肌细胞中的HSP70表达,以保护细胞在热应激期间

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We investigated the effects of co-enzyme Q10 (Q10) and acetyl salicylic acid (ASA) on expression of Hsp70 in the protection of primary chicken myocardial cells during heat stress. Western blot analysis showed that Q10 and ASA accelerated the induction of Hsp70 when chicken myocardial cells were exposed to hyperthermia. In the absence of heat stress, however, neither Q10 nor ASA are able to upregulate Hsp70 expression. Analysis of enzymes that respond to cellular damage and pathological examination revealed that ectopic expression of ASA and Q10 alleviate cellular damage during heat stress. Quantification of heat shock factors (HSF) indicated that treatment of ASA increased the expression of HSF-1 and HSF-3 during heat stress. Treatment with Q10 resulted in the elevation of HSF-1 expression. Expression of HSF-2 and HSF-4 was not affected by ASA or Q10. Subcellular distribution analysis of HSF-1 and HSF-3 showed that in response to heat stress ASA promoted nuclear translocation of HSF-1 and HSF-3, while Q10 promoted only HSF-1 nuclear translocation. Chromatin immunoprecipitation (ChIP) analysis indicated that HSF-1 occupies the Hsp70 promoter in chicken primary myocardial cells during heat stress and under normal conditions, while HSF-3 occupies the Hsp70 promoter only during heat stress. Real-time PCR analysis revealed that ASA induces HSF-1 and HSF-3 binding to Hsp70 HSE, while Q10 only induces HSF1 binding to Hsp70 HSE, in agreement with the impact of HSF1 and HSF3 silencing on Hsp70 expression. These data demonstrate that ASA and Q10 both induce the expression of Hsp70 to protect chicken primary myocardial cells during heat stress, but through distinct pathways.
机译:我们研究了共酶Q10(Q10)和乙酰水杨酸(ASA)对HSP70在热应激期间初级鸡心肌细胞的表达中的影响。 Western印迹分析表明,当鸡心肌细胞暴露于热疗时,Q10和ASA加速了HSP70的诱导。然而,在没有热应激的情况下,Q10和ASA都不能够上调HSP70表达。响应细胞损伤和病理检查的酶分析表明,ASA和Q10的异位表达缓解热应激期间的细胞损伤。热休克因子的定量(HSF)表明ASA的处理在热应激期间增加了HSF-1和HSF-3的表达。用Q10治疗导致HSF-1表达的升高。 HSF-2和HSF-4的表达不受ASA或Q10的影响。 HSF-1和HSF-3的亚细胞分布分析表明,响应于热应激ASA促进HSF-1和HSF-3的核转位,而Q10仅促进了HSF-1核易位。染色质免疫沉淀(芯片)分析表明,HSF-1在热应激期间患者鸡初级心肌细胞中的HSP70启动子,而HSF-3仅在热应激期间仅占据HSP70启动子。实时PCR分析显示,ASA诱导HSF-1和HSF-3与HSP70 HSE结合,而Q10仅诱导HSF1与HSP70 HSE结合,同意HSF1和HSF3沉默对HSP70表达的影响。这些数据表明,ASA和Q10均诱导HSP70的表达,以在热应激期间保护鸡初级心肌细胞,而是通过不同的途径。

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