Department of Intensive Care Unit, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Department of Intensive Care Unit, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Biomed Pharmacother. 2019 Jun;114:108815. doi: 10.1016/j.biopha.2019.108815. Epub 2019 Apr 5.
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 °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.
本研究旨在探讨羟甲香豆素 A(HSYA)对热应激(HS)后神经干细胞(NSC)的作用机制。将大鼠 NSC 细胞在 42°C 下培养以施加热应激。使用细胞计数试剂盒-8 和 Edu 测定法分析 NSC 增殖。使用 Annexin V/PI 凋亡试剂盒检测 NSC 凋亡。通过 Western blot 测定自噬和凋亡相关蛋白的表达和磷酸化。结果表明,HSYA 可显著促进热应激后 NSC 的增殖并减轻其凋亡。HSYA 还增加了热应激诱导的 NSCs 中 Bcl-2 的表达,但降低了 Bax 和 cleaved caspase-3 的表达。此外,HSYA 降低了热应激后 p38 和 Hsp27-78 的磷酸化和 MK-2 的表达,这与 SB203850 处理或 p38 敲低的 NSCs 一致。此外,我们证明热应激增加了 NSCs 中 LC3-II 的表达和 mTOR 的磷酸化,并降低了 p62 的表达,而 HSYA、SB203850 处理或 p38 敲低可逆转这些变化。总之,HSYA 通过下调 MK2 表达和 p38 和 Hsp27-78 的磷酸化,显著逆转了热应激诱导的 NSC 凋亡和自噬(P<0.05)。