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蓝光诱导与活性氧相关的神经肽受体 PAC1-R 的核易位,与其自身的上调有关。

Blue light induces the nuclear translocation of neuropeptide receptor PAC1-R associated with the up-regulation of PAC1-R its own in reactive oxygen species associated way.

机构信息

Department of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong, China; Guangdong Province Key Laboratory of Bioengineering Medicine, Guangdong, China; Guangdong Provincial Biotechnology Drug & Engineering Technology Research Center, Guangdong, China; National Engineering Research Center of Genetic Medicine, Guangdong, China.

Department of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong, China.

出版信息

Biochim Biophys Acta Gen Subj. 2021 Jun;1865(6):129884. doi: 10.1016/j.bbagen.2021.129884. Epub 2021 Feb 26.

Abstract

PAC1-R is neuropeptide PACAP (pituitary adenylate cyclase activating polypeptide) preferring receptor mediates the antioxidant and cytoprotective effects of PACAP. It was found in this research that in both PAC1R-CHO cells with high expression of PAC1R-eGFP and retinal ganglion cells (RGC-5) with natural expression of PAC1-R, blue light and hydrogen peroxide (HO) trigger the significant nuclear translocation of PAC1-R, and the nuclear translocation of PAC1-R was positive correlation with the up-regulation of expression level and promoter activity of PAC1-R its own, while red light worked much less efficiently than blue light. Reactive oxygen species (ROS) scavenger NAC (N-acetyl-L-cysteine) and palmitoylation inhibitor 2-bromopalmitate (2-BP) disturbed the nuclear shifting associated with the correlative up-regulation of PAC1 significantly, and PAC1-R mutant (M-PAC1-R) on Cys25/Ala25 displayed the significant decreased nuclear trafficking efficiency. Furthermore, the Western Blot results with the antibody raised against the C-terminal of PAC1-R showing PAC1-R in the nucleus was fragmentation hinting that C-terminal of PAC1-R with theoretical nuclear location signal (NLS) may be involved in activation of PAC1-R promoter in the nucleus. All above results indicated that PAC1-R makes the nuclear translocation to trigger the activation of PAC1-R itself promoter resulting into the up-regulation of of PAC1-R in response to the oxidative stress induced by blue light and ROS such as HO .

摘要

PAC1-R 是神经肽 PACAP(垂体腺苷酸环化酶激活肽)的优先受体,介导 PACAP 的抗氧化和细胞保护作用。本研究发现,在高表达 PAC1R-eGFP 的 PAC1R-CHO 细胞和自然表达 PAC1-R 的视网膜神经节细胞(RGC-5)中,蓝光和过氧化氢(HO)触发 PAC1-R 的显著核转位,PAC1-R 的核转位与 PAC1-R 自身表达水平和启动子活性的上调呈正相关,而红光的作用远不及蓝光。活性氧(ROS)清除剂 NAC(N-乙酰-L-半胱氨酸)和棕榈酰化抑制剂 2-溴棕榈酸(2-BP)干扰了与 PAC1 相关的上调相关的核移位,并且 Cys25/Ala25 上的 PAC1-R 突变体(M-PAC1-R)显示出明显降低的核转运效率。此外,用针对 PAC1-R C 端的抗体进行的 Western Blot 结果显示,PAC1-R 在核内发生片段化,提示具有理论核定位信号(NLS)的 PAC1-R C 端可能参与激活核内的 PAC1-R 启动子。上述结果表明,PAC1-R 发生核转位,触发 PAC1-R 自身启动子的激活,导致 PAC1-R 在蓝光和 ROS(如 HO)引起的氧化应激下的上调。

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