Smith M D, Ensor E A, Kinloch R A, Latchman D S
Medical Molecular Biology Unit, Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK.
Neuroreport. 2001 Oct 29;12(15):3183-8. doi: 10.1097/00001756-200110290-00008.
We have demonstrated previously that exogenously expressed Brn-3a is capable of protecting neurons of the peripheral nervous system against apoptosis. In these previous studies Brn-3a showed a degree of neuronal sub-type specificity, in that while it could promote survival in NGF-dependent sensory neurons, no effect was observed in NGF-dependent neurons of the sympathetic nervous system. In this report, we show that Brn-3a delivered using a herpes simplex virus is capable of protecting cultures of rat cerebrocortical neurons of the central nervous system against two types of cell death stimuli, including glutamate neurotoxicity. Hence the protective effect of Brn-3a is not confined to neurons of the peripheral nervous system but can also occur in neurons of the CNS.
我们之前已经证明,外源性表达的Brn-3a能够保护外周神经系统的神经元免于凋亡。在这些先前的研究中,Brn-3a表现出一定程度的神经元亚型特异性,即虽然它可以促进NGF依赖的感觉神经元的存活,但在交感神经系统的NGF依赖神经元中未观察到效果。在本报告中,我们表明,使用单纯疱疹病毒递送的Brn-3a能够保护中枢神经系统的大鼠脑皮质神经元培养物免受两种类型的细胞死亡刺激,包括谷氨酸神经毒性。因此,Brn-3a的保护作用不仅限于外周神经系统的神经元,也可发生在中枢神经系统的神经元中。