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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Hydroxysafflor yellow A (HSYA) alleviates apoptosis and autophagy of neural stem cells induced by heat stress via p38 MAPK/MK2/Hsp27-78 signaling pathway
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Hydroxysafflor yellow A (HSYA) alleviates apoptosis and autophagy of neural stem cells induced by heat stress via p38 MAPK/MK2/Hsp27-78 signaling pathway

机译:Hydroxafeafflor黄色A(HSYA)通过P38 MAPK / MK2 / HSP27-78信号通路通过P38 Mapk / MK2 / Hsp27-78发信号通路来缓解热应激诱导的神经干细胞的凋亡和自噬

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摘要

This study aimed to explore mechanisms of the effects of hydroxysafflor yellow A (HSYA) on neural stem cells (NSCs) after heat stress (HS). Rat NSCs cells were cultured at 42 degrees C to impose heat stress. Cell counting kit-8 and Edu assay were used to analyze NSC proliferation. Annexin V/PI apoptosis kit was used to detect NSC apoptosis. Expression and phosphorylation of autophagy and apoptosis-associated proteins were determined by western blotting. We showed that HSYA significantly promoted proliferation and attenuated apoptosis of NSCs after heat stress. HSYA also increased Bcl-2 expression but decreased the expression of Bax and cleaved caspase-3 in NSCs induced by heat stress. In addition, HSYA decreased p38 and Hsp27-78 phosphorylation and MK-2 expression after heat stress, which was consistent with NSCs treated with SB203850 treatment or p38 knockdown. Furthermore, we demonstrated that heat stress increased LC3-II expression and mTOR phosphorylation, and decreased the expression of p62 in NSCs, while HSYA, SB203850 treatment or p38 knockdown reversed these alterations. In conclusion, HSYA significantly reversed the apoptosis and autophagy of NSCs induced by heat stress (P < 0.05), via downregulating MK2 expression and p38 and Hsp27-78 phosphorylation.
机译:本研究旨在探讨热应激后羟烷烃黄A(HSYA)对神经干细胞(NSCs)的影响的机制。在42℃下培养大鼠NSCs细胞以施加热应激。用于分析NSC增殖的细胞计数试剂盒和EDU测定。 Annexin V / PI细胞凋亡试剂盒用于检测NSC凋亡。通过蛋白质印迹测定自噬和凋亡相关蛋白的表达和磷酸化。我们表明,HSSYA在热应激后显着促进了NSCs的增殖和减毒凋亡。 HSESA也增加了BCL-2表达,但减少了通过热应激诱导的NSC中的BAX和切割的caspase-3的表达。此外,HSSEA在热应激后降低P38和HSP27-78磷酸化和MK-2表达,这与用SB203850处理或P38敲低处理的NSCs一致。此外,我们证明了热应激增加的LC3-II表达和MTOR磷酸化,并降低了NSCs中P62的表达,而HSYA,SB203850治疗或P38敲低逆转这些改变。总之,HSYA通过下调MK2表达和P38和HSP27-78磷酸化显着逆转了由热应激(P <0.05)引起的NSCs的凋亡和自噬。

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