Center of Research Laboratory, Lianyungang Hospital Affiliated to Xuzhou Medical College, 182 Tongguan Road, Lianyungang 222001, China; Deparment of Clinical Laboratory Diagnostics,Kangda College of Nanjing Medical University, Lianyungang 222000, China.
Center of Research Laboratory, Lianyungang Hospital Affiliated to Xuzhou Medical College, 182 Tongguan Road, Lianyungang 222001, China.
Life Sci. 2016 Jul 15;157:152-157. doi: 10.1016/j.lfs.2016.06.005. Epub 2016 Jun 7.
To investigate the roles of neutrophil alkaline phosphatase (NAP) in the migration, reactive oxygen species (ROS) generation and apoptosis of neutrophils.
NAP was overexpressed in neutrophil-like differentiated HL-60 cells via transfecting coding sequence of NAP by lentivirus. NAP overexpression in HL-60 cells was confirmed by the methods of quantitative RT-PCR and Western blotting. HL-60 cells were induced to differentiate into neutrophil-like cells by exposure to 1.5% dimethylsulfoxide (DMSO). The migration of neutrophil-like cells were detected by Transwell migration assay. ROS generation of neutrophil-like cells were determined by flow cytometry. Neutrophil-like cells continued to be cultured for 24h, and were then harvested for apoptosis and Western blotting.
After GFP-NAP infection by lentivirus, the expression of NAP was up-regulated in HL-60 cells. HL-60 cells were allowed to differentiate into neutrophil-like cells after 5-day exposure to 1.5% DMSO. Overexpression of NAP in neutrophil-like cells resulted in an increase in the number of migrated cells, intracellular ROS and cell apoptosis followed by a rise in the expression of Caspase 3, Caspase 9 and Bax, while those results were reversed in the NEG and CON group.
NAP might play a critical role in the anti-microbial function of neutrophils by promoting its migration and ROS generation, as well as accelerating apoptosis in neutrophils.
研究中性粒细胞碱性磷酸酶(NAP)在中性粒细胞迁移、活性氧(ROS)生成和凋亡中的作用。
通过慢病毒转染编码 NAP 的序列,在 HL-60 细胞中过表达 NAP。通过定量 RT-PCR 和 Western blot 方法证实 HL-60 细胞中 NAP 的过表达。将 HL-60 细胞暴露于 1.5%二甲基亚砜(DMSO)中诱导分化为中性粒细胞样细胞。通过 Transwell 迁移实验检测中性粒细胞样细胞的迁移。通过流式细胞术测定中性粒细胞样细胞 ROS 的生成。继续培养中性粒细胞样细胞 24 小时,然后进行凋亡和 Western blot 分析。
经慢病毒 GFP-NAP 感染后,HL-60 细胞中 NAP 的表达上调。HL-60 细胞在 1.5% DMSO 作用 5 天后分化为中性粒细胞样细胞。在中性粒细胞样细胞中过表达 NAP 导致迁移细胞数量、细胞内 ROS 和细胞凋亡增加,同时 Caspase 3、Caspase 9 和 Bax 的表达也随之升高,而 NEG 和 CON 组则出现相反的结果。
NAP 可能通过促进中性粒细胞的迁移和 ROS 生成,并加速中性粒细胞凋亡,在中性粒细胞的抗菌功能中发挥关键作用。