Kim Jung Hee, Lee Tae Young, Yoo Kyung Hyun, Lee Hyo Soo, Cho Sun A, Park Jong Hoon
Department of Biological Science, Sookmyung Women's University, Seoul, Korea.
BMB Rep. 2008 Feb 29;41(2):146-52. doi: 10.5483/bmbrep.2008.41.2.146.
In the presence of NGF, PC12 cells extend neuronal processes, cease cell division, become electrically excitable, and undergo several biochemical changes that are detectable in developing sympathetic neurons. We investigated the expression pattern of the apoptosis-related genes at each stage of neuronal differentiation using a cDNA microarray containing 320 apoptosis-related rat genes. By comparing the expression patterns through time-series analysis, we identified candidate genes that appear to regulate neuronal differentiation. Among the candidate genes, HO2 was selected by real-time PCR and Western blot analysis. To identify the roles of selected genes in the stages of neuronal differentiation, transfection of HO2 siRNA in PC12 cells was performed. Down-regulation of HO2 expression causes a reduction in neuronal differentiation in PC12 cells. Our results suggest that the HO2 gene could be related to the regulation of neuronal differentiation levels.
在神经生长因子(NGF)存在的情况下,嗜铬细胞瘤(PC12)细胞伸出神经突,停止细胞分裂,变得具有电兴奋性,并经历一些在发育中的交感神经元中可检测到的生化变化。我们使用包含320个大鼠凋亡相关基因的cDNA微阵列,研究了神经元分化各阶段凋亡相关基因的表达模式。通过时间序列分析比较表达模式,我们鉴定出了似乎调控神经元分化的候选基因。在这些候选基因中,通过实时定量聚合酶链反应(real-time PCR)和蛋白质免疫印迹分析(Western blot analysis)选择了HO2基因。为了确定所选基因在神经元分化阶段的作用,我们在PC12细胞中进行了HO2小干扰RNA(siRNA)转染。HO2表达的下调导致PC12细胞中神经元分化减少。我们的结果表明,HO2基因可能与神经元分化水平的调控有关。