Department of Cellular Biophysics, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
Neurochem Res. 2011 Aug;36(8):1482-9. doi: 10.1007/s11064-011-0474-6. Epub 2011 Apr 21.
To explore how long the gene-silencing effects of siRNA introduced into postmitotic neurons continue, we transferred siRNA against GFP into GFP-expressing Purkinje and Golgi cells in cerebellar cell cultures by single-cell electroporation. The temporal changes in the intensity of GFP fluorescence in the same electroporated cells were monitored in real time using GFP imaging. Under standard conditions, GFP fluorescence was reduced to under one-tenth of the initial levels 4-7 days after electroporation. Such effects continued at least up to 14 days after electroporation. The effects of siRNAs against endogenous genes also continued for the same period. Thus, this method could be an effective tool for silencing gene expression for a long period in postmitotic neurons.
为了探究递送至有丝分裂后神经元的 siRNA 的基因沉默效应能持续多久,我们通过单细胞电穿孔将针对 GFP 的 siRNA 转入小脑细胞培养物中 GFP 表达的浦肯野细胞和高尔基细胞内。使用 GFP 成像实时监测同一电穿孔细胞内 GFP 荧光强度的时变情况。在标准条件下,电穿孔后 4-7 天 GFP 荧光强度降低到初始水平的十分之一以下。这种效应至少持续到电穿孔后 14 天。针对内源性基因的 siRNAs 的效应也持续了相同的时间。因此,该方法可能成为在有丝分裂后神经元中长时间沉默基因表达的有效工具。