Allsopp T E, Kiselev S, Wyatt S, Davies A M
School of Biological and Medical Sciences, St Andrews University, Fife, UK.
Eur J Neurosci. 1995 Jun 1;7(6):1266-72. doi: 10.1111/j.1460-9568.1995.tb01116.x.
Developing neurons die if they fail to obtain an adequate supply of neurotrophins from their targets but how neurotrophins suppress cell death is not known. Although over-expression of exogenous Bcl-2 can prevent the death of cultured neurons deprived of members of the nerve growth factor family of neurotrophins it is not known if this effect is physiologically relevant. To determine if Bcl-2 participates in the neurotrophin survival response we used antisense bcl-2 RNA to inhibit endogenous Bcl-2 expression. Here we show that brain-derived neurotrophic factor (BDNF)-dependent neurons are killed by antisense bcl-2 RNA in the presence of BDNF. However, when these neurons were supported with ciliary neurotrophic factor (CNTF) their survival was not affected by antisense bcl-2 RNA. Likewise, the survival of CNTF-dependent ciliary neurons was not affected by antisense bcl-2 RNA. Our findings suggest that Bcl-2 is required for the BDNF survival response and that alternative, Bcl-2-independent survival mechanisms operate in sensory and parasympathetic neurons exposed to CNTF.
发育中的神经元如果无法从其靶细胞获得足够的神经营养因子供应就会死亡,但神经营养因子如何抑制细胞死亡尚不清楚。虽然外源性Bcl-2的过表达可以防止被剥夺神经营养因子神经生长因子家族成员的培养神经元死亡,但这种作用在生理上是否相关尚不清楚。为了确定Bcl-2是否参与神经营养因子的存活反应,我们使用反义bcl-2 RNA来抑制内源性Bcl-2的表达。我们在此表明,在存在脑源性神经营养因子(BDNF)的情况下,反义bcl-2 RNA会杀死依赖BDNF的神经元。然而,当这些神经元由睫状神经营养因子(CNTF)支持时,它们的存活不受反义bcl-2 RNA的影响。同样,依赖CNTF的睫状神经元的存活也不受反义bcl-2 RNA的影响。我们的研究结果表明,Bcl-2是BDNF存活反应所必需的,并且在暴露于CNTF的感觉神经元和副交感神经元中存在替代的、不依赖Bcl-2的存活机制。