Narayan Sujatha, Greif Karen F
Department of Biology, Bryn Mawr College, 101 North Merion Avenue, Bryn Mawr, PA 19010, USA.
J Neurosci Methods. 2004 Feb 15;133(1-2):91-8. doi: 10.1016/j.jneumeth.2003.10.002.
Developing neurons are engaged in neurite outgrowth as well as the synthesis and transport of proteins involved in synaptic transmission. Very little is known about when transport is established in these rudimentary neurites. We used a novel technique to visualize protein transport during the early hours of neurite outgrowth in culture. Recombinant adenoviruses were used to express a synaptotagmin-YFP fusion protein in the superior cervical ganglia of neonatal rats in vivo and protein transport was examined in neuronal cultures established from the superior cervical ganglions (SCGs). We find that, as early as 4h in culture, synaptotagmin-YFP was present in the cytoplasm, lamellipodia, filopodia and growth cones. Protein expression appeared punctate in neurites at 8h in vitro and is consistent with a vesicular localization. These results indicate that the machinery to transport synapse-specific proteins is functional in rudimentary neurites at this time and indicates that this technique can be used to study early neuronal development.
正在发育的神经元参与神经突生长以及与突触传递相关的蛋白质的合成和运输。对于这些原始神经突中何时建立运输,人们了解甚少。我们使用了一种新技术来观察培养过程中神经突生长早期的蛋白质运输。重组腺病毒用于在新生大鼠体内的颈上神经节中表达突触结合蛋白-YFP融合蛋白,并在从颈上神经节(SCGs)建立的神经元培养物中检测蛋白质运输。我们发现,早在培养4小时时,突触结合蛋白-YFP就存在于细胞质、片状伪足、丝状伪足和生长锥中。在体外培养8小时时,神经突中的蛋白质表达呈点状,这与囊泡定位一致。这些结果表明,此时运输突触特异性蛋白质的机制在原始神经突中起作用,并且表明该技术可用于研究早期神经元发育。