Wang Yinna, Ma Haihao, Liu Zheming, Zhao Piao, Liu Jia, Zhu Hang, Zhou Yong, Man Yilong, Zhou Xiaomao
Longping Branch, College of Biology, Hunan University, Changsha 410125, China.
College of Forestry, Central South University of Forestry and Technology, Changsha 410004, China.
Int J Mol Sci. 2025 Mar 26;26(7):3042. doi: 10.3390/ijms26073042.
Cell lines and their corresponding expression plasmids are extensively utilized in the study of insect physiology and pathology. In this research, four single-cell cultured lines (Px4-1 to Px4-4) of were established from eggs. The promoter for the (PxEF1α), known for its high driving activity in cells, was cloned and used to construct expression plasmids. Dual-luciferase activity assays and EGFP expression analyses demonstrated that the PxEF1α promoter exhibited the strongest driving activity in Px4-2 cells, comparable to that of the immediate-early 1 promoter associated with the homologous region 5 enhancer (AcIE1) from the multicapsid nucleopolyhedrovirus (AcMNPV). In contrast, the driving activity of PxEF1α in cells derived from , , and was lower. Furthermore, the PxEF1α promoter was successfully employed to drive inward rectifier potassium 2A (Kir2A) expression in Px4-2 cells. The electrophysiological properties of the insect Kir2A channel were successfully characterized for the first time. It was observed that the PxKir2A channel possesses typical inward rectifier potassium channel properties and can be inhibited by nanomolar concentrations of VU625 and VU590. This study offers a novel approach for the expression and investigation of foreign gene function in insect cells and provides a valuable tool for the in-depth study of key biomolecules in .
细胞系及其相应的表达质粒在昆虫生理学和病理学研究中被广泛应用。在本研究中,从卵中建立了四个单细胞培养系(Px4-1至Px4-4)。克隆了在细胞中具有高驱动活性的(PxEF1α)启动子,并用于构建表达质粒。双荧光素酶活性测定和EGFP表达分析表明,PxEF1α启动子在Px4-2细胞中表现出最强的驱动活性,与来自多角体核多角体病毒(AcMNPV)的同源区域5增强子(AcIE1)相关的立即早期1启动子相当。相比之下,PxEF1α在源自、和的细胞中的驱动活性较低。此外,PxEF1α启动子成功用于驱动Px4-2细胞中内向整流钾2A(Kir2A)的表达。首次成功表征了昆虫Kir2A通道的电生理特性。观察到PxKir2A通道具有典型的内向整流钾通道特性,并且可以被纳摩尔浓度的VU625和VU590抑制。本研究为昆虫细胞中外源基因功能的表达和研究提供了一种新方法,并为深入研究中的关键生物分子提供了有价值的工具。