Li Ran, Wang Yong, Yang Zhaofei, He Yunling, Zhao Tong, Fan Ming, Wang Xuan, Zhu Lingling, Wang Xiaomin
Department of Physiology, Key Laboratory for Neurodegenerative Disorders of the Ministry of Education, Capital Medical University, 10# You An Men, Beijing, 100069, People's Republic of China.
Cell Stress Chaperones. 2015 May;20(3):507-16. doi: 10.1007/s12192-015-0575-2. Epub 2015 Feb 4.
Hypoxia is an important factor in regulation of cell behavior both under physiological and pathological conditions. The mechanisms of hypoxia-induced cell death have not been completely elucidated yet. It is well known that Ca(2+) is critically related to cell survival. Hypoxia-inducible factor-1α (HIF-1α) is a core regulatory factor during hypoxia, and L-type voltage-dependent Ca(2+) channels (L-VDCCs) have been reported to play a critical role in cell survival. This study was conducted to explore the relationship between L-VDCC expression and HIF-1α regulation in PC12 cells under hypoxia. PC12 cells were treated at 20 or 3 % O2 to observe its proliferation and the intracellular calcium concentration. Then, we detected the protein expression of HIF-1α and L-VDCCs subtypes, Cav1.2 and Cav1.3. At last, to verify the relationship between HIF-1α and Cav1.2 and Cav1.3, we got the expression of Cav1.2 and Cav1.3 with Western blot and luciferase report gene assays after PC12 cells were treated by echinomycin, which is an HIF-1α inhibitor. Compared with 20 % O2 (normoxia), 3 % O2 (hypoxia) inhibited cell proliferation, increased the intracellular calcium concentration, and induced protein expression of HIF-1α. The protein expression of two L-VDCCs subtypes expressed in the nervous system, Cav1.2 and Cav1.3, was upregulated by hypoxia and reduced dose dependently by treatment with echinomycin, a HIF-1α inhibitor. Luciferase report gene assays showed that the expression of Cav1.2 and Cav1.3 genes was augmented under 3 % O2. However, echinomycin only slightly and dose dependently decreased expression of the Cav1.2 gene, but not that of the Cav1.3 gene. These data indicated that Cav1.2 might be regulated by HIF-1α as one of its downstream target genes and involved in regulation of PC12 cells death under hypoxia.
缺氧是生理和病理条件下调节细胞行为的重要因素。缺氧诱导细胞死亡的机制尚未完全阐明。众所周知,Ca(2+)与细胞存活密切相关。缺氧诱导因子-1α(HIF-1α)是缺氧过程中的核心调节因子,据报道L型电压依赖性Ca(2+)通道(L-VDCCs)在细胞存活中起关键作用。本研究旨在探讨缺氧条件下PC12细胞中L-VDCC表达与HIF-1α调节之间的关系。将PC12细胞置于20%或3% O2条件下处理,以观察其增殖及细胞内钙浓度变化。然后,检测HIF-1α和L-VDCCs亚型Cav1.2和Cav1.3的蛋白表达。最后,为验证HIF-1α与Cav1.2和Cav1.3之间的关系,在用棘霉素(一种HIF-1α抑制剂)处理PC12细胞后,通过蛋白质印迹法和荧光素酶报告基因检测来检测Cav1.2和Cav1.3 的表达。与20% O2(常氧)相比,3% O2(缺氧)抑制细胞增殖,增加细胞内钙浓度,并诱导HIF-1α蛋白表达上调。在神经系统中表达的两种L-VDCCs亚型Cav1.2和Cav1.3 的蛋白表达在缺氧时上调,而用HIF-1α抑制剂棘霉素处理后呈剂量依赖性降低。荧光素酶报告基因检测显示,在3% O2条件下Cav1.2和Cav1.3基因的表达增强,但棘霉素仅轻微且呈剂量依赖性地降低Cav1.2基因的表达,而对Cav1.3基因的表达无影响。这些数据表明,Cav1.2可能作为HIF-1α的下游靶基因之一受其调控,并参与缺氧条件下PC12细胞死亡调控。