Krüttgen A, Möller J C, Heymach J V, Shooter E M
Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305-5125, USA.
Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9614-9. doi: 10.1073/pnas.95.16.9614.
Recent studies have established that neurotrophin synthesis and secretion are regulated by activity and that these factors are involved in activity-dependent processes in the nervous system. Neurotrophins also are known to induce increases in intracellular calcium, a trigger for regulated secretion. This finding raises the possibility that neurotrophins themselves may stimulate regulated secretion of neurotrophins. To address this question, we studied the release of neurotrophins from transfected PC12 cells, a widely used model for neuronal secretion and neurotrophin signal transduction. We found that neurotrophins induced the regulated secretion of brain-derived neurotrophic factor, neurotrophin-3 (NT-3), and neurotrophin-4/5. The effect of brain-derived neurotrophic factor on release of NT-3 could be abolished by REX, a p75 blocking antibody, but not by K252a, an inhibitor of neurotrophin tyrosine kinase receptor (Trk) signaling. The nerve growth factor effect on release of NT-3 could be blocked only by simultaneous application of REX and K252a, suggesting that they are mediated by TrkA as well as p75. Our data show that neurotrophins are able to induce the regulated secretion of neurotrophins and suggest a signal-transducing role for both TrkA and p75 in this process. The neurotrophin-induced release of neurotrophins may be relevant for activity-dependent processes such as synaptic plasticity and memory formation.
最近的研究证实,神经营养因子的合成和分泌受活性调节,并且这些因子参与神经系统中依赖活性的过程。已知神经营养因子还会诱导细胞内钙增加,这是调节分泌的触发因素。这一发现增加了神经营养因子自身可能刺激神经营养因子调节分泌的可能性。为了解决这个问题,我们研究了转染的PC12细胞中神经营养因子的释放,PC12细胞是神经元分泌和神经营养因子信号转导中广泛使用的模型。我们发现神经营养因子诱导了脑源性神经营养因子、神经营养因子-3(NT-3)和神经营养因子-4/5的调节分泌。脑源性神经营养因子对NT-3释放的影响可被p75阻断抗体REX消除,但不能被神经营养因子酪氨酸激酶受体(Trk)信号抑制剂K252a消除。神经生长因子对NT-3释放的影响只有在同时应用REX和K252a时才能被阻断,这表明它们是由TrkA以及p75介导的。我们的数据表明神经营养因子能够诱导神经营养因子的调节分泌,并提示TrkA和p75在此过程中具有信号转导作用。神经营养因子诱导的神经营养因子释放可能与突触可塑性和记忆形成等依赖活性的过程相关。