Friedman W J
Department of Pathology, Taub Institute for the Study of Alzheimer's Disease and the Aging Brain, and the Center for Neurobiology and Behavior, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
J Neurosci. 2000 Sep 1;20(17):6340-6. doi: 10.1523/JNEUROSCI.20-17-06340.2000.
Nerve growth factor (NGF) and related neurotrophins influence neuronal survival and differentiation via interactions with the trk family of receptors. Recent studies have demonstrated that neurotrophins may also induce cell death via the p75 receptor. The importance and generality of neurotrophin-induced death in the brain have not been defined but may play a critical role during development and in disease-associated neuronal death. Here we demonstrate for the first time that all four members of the neurotrophin family directly elicit the death of hippocampal neurons via the p75 receptor. The hippocampus is a complex structure with many different neuronal subpopulations, and signals that influence neuronal death during development may have a critical impact on the mature function of this structure. In these studies we show that each neurotrophin causes the death of hippocampal neurons expressing p75 but lacking the cognate trk receptor. Neurotrophin-induced neuronal death is mediated by activation of Jun kinase. These studies demonstrate that neurotrophins can regulate death as well as survival of CNS neurons.
神经生长因子(NGF)及相关神经营养因子通过与trk受体家族相互作用来影响神经元的存活和分化。最近的研究表明,神经营养因子也可能通过p75受体诱导细胞死亡。神经营养因子诱导的脑内细胞死亡的重要性和普遍性尚未明确,但可能在发育过程以及与疾病相关的神经元死亡中起关键作用。在此,我们首次证明神经营养因子家族的所有四个成员均可通过p75受体直接引发海马神经元死亡。海马是一个具有许多不同神经元亚群的复杂结构,在发育过程中影响神经元死亡的信号可能对该结构的成熟功能产生关键影响。在这些研究中,我们表明每种神经营养因子都会导致表达p75但缺乏相应trk受体的海马神经元死亡。神经营养因子诱导的神经元死亡是由Jun激酶的激活介导的。这些研究表明,神经营养因子可以调节中枢神经系统神经元的死亡以及存活。