Aibel L, Martin-Zanca D, Perez P, Chao M V
Skirball Institute, New York University Medical Center, New York 10016, USA.
J Neurosci Res. 1998 Nov 1;54(3):424-31. doi: 10.1002/(SICI)1097-4547(19981101)54:3<424::AID-JNR13>3.0.CO;2-6.
Nerve growth factor (NGF) initiates its biological effects by promoting the dimerization and activation of the tyrosine kinase receptor TrkA. The requirements for NGF signaling through the TrkA receptor have been defined extensively from studies in immortalized cells, involving transfection of NIH 3T3, COS, and PC12 cells. In the present study, we tested the effects of extracellular and intracellular mutations of TrkA after DNA-mediated transfection in primary cultures of embryonic day 17 hippocampal neurons. We found that the action of the TrkA receptor on neuronal differentiation depends on specific motifs in the extracellular domain and on tyrosine 490 (Y490), the site for SHC protein binding. In contrast with previous observations in a PC12 background, a mutation in the SHC Y490 binding site in TrkA resulted in a loss of NGF-dependent process formation. These results indicate that tyrosine 490 is necessary for neurite outgrowth in hippocampal neurons. Moreover, a constitutively active form of TrkA did not give enhanced responsiveness in hippocampal neurons, indicating that the behavior of TrkA receptors in primary neuronal cells is distinct from that of other cell types.
神经生长因子(NGF)通过促进酪氨酸激酶受体TrkA的二聚化和激活来启动其生物学效应。通过对永生化细胞(包括NIH 3T3、COS和PC12细胞的转染)的研究,已广泛确定了通过TrkA受体进行NGF信号传导的要求。在本研究中,我们在胚胎第17天海马神经元的原代培养物中进行DNA介导的转染后,测试了TrkA细胞外和细胞内突变的影响。我们发现,TrkA受体对神经元分化的作用取决于细胞外结构域中的特定基序以及SHC蛋白结合位点酪氨酸490(Y490)。与之前在PC12背景下的观察结果相反,TrkA中SHC Y490结合位点的突变导致NGF依赖性突起形成丧失。这些结果表明,酪氨酸490对于海马神经元的轴突生长是必需的。此外,组成型激活形式的TrkA在海马神经元中并未表现出增强的反应性,这表明TrkA受体在原代神经元细胞中的行为与其他细胞类型不同。