Cheng Shanshan, Zhang Chen, Xu Congyu, Wang Long, Zou Xiaoxia, Chen Guiquan
Model Animal Research Center, MOE Key Laboratory of Model Animal for Disease Study, Nanjing Biomedical Research Institute, Nanjing University, 12 Xuefu Road, Nanjing, Jiangsu Province 210061, China.
Model Animal Research Center, MOE Key Laboratory of Model Animal for Disease Study, Nanjing Biomedical Research Institute, Nanjing University, 12 Xuefu Road, Nanjing, Jiangsu Province 210061, China.
Int J Biochem Cell Biol. 2014 Dec;57:186-96. doi: 10.1016/j.biocel.2014.10.029. Epub 2014 Nov 3.
Impairment in the microRNA (miRNA) network causes a number of neurodegenerative diseases. Endoribonuclease Dicer is a key RNase to produce mature miRNAs. It has been shown that Dicer is important for the maintenance of excitatory neuron survival during early postnatal period. However, the role of Dicer in adult mature excitatory neuron survival is not clear. In this study, we generated a mouse model in which Dicer is conditionally inactivated in forebrain excitatory neurons from a mature stage, and this line is termed Dicer conditional knockout (cKO). Significant age-dependent neurodegeneration was observed in the cortex of Dicer cKO mice, indicating an important role of Dicer in the maintenance of mature excitatory neuron survival in the adult cortex. Impairment in adult neurogenesis was found in 6-month but not in young Dicer cKO mice. However, astrocytosis was detected in young Dicer cKO mice displaying no apparent neuron loss. Overall, neurogenesis impairment and neuroinflammation may play pivotal roles in the progression of neurodegeneration.
微小RNA(miRNA)网络的损伤会引发多种神经退行性疾病。核糖核酸内切酶Dicer是产生成熟miRNA的关键核糖核酸酶。研究表明,Dicer对于出生后早期兴奋性神经元存活的维持至关重要。然而,Dicer在成年成熟兴奋性神经元存活中的作用尚不清楚。在本研究中,我们构建了一种小鼠模型,其中Dicer在成熟阶段的前脑兴奋性神经元中被条件性失活,该品系被称为Dicer条件性敲除(cKO)小鼠。在Dicer cKO小鼠的皮质中观察到显著的年龄依赖性神经退行性变,表明Dicer在维持成年皮质中成熟兴奋性神经元存活方面具有重要作用。在6个月大的Dicer cKO小鼠中发现成年神经发生受损,但年轻小鼠未出现这种情况。然而,在未出现明显神经元丢失的年轻Dicer cKO小鼠中检测到星形胶质细胞增生。总体而言,神经发生损伤和神经炎症可能在神经退行性变的进展中起关键作用。