Department of Genetics, Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Neurosci. 2013 Jan 2;33(1):35-51. doi: 10.1523/JNEUROSCI.0245-12.2013.
The use of neurotropic viruses as transsynaptic tracers was first described in the 1960s, but only recently have such viruses gained popularity as a method for labeling neural circuits. The development of retrograde monosynaptic tracing vectors has enabled visualization of the presynaptic sources onto defined sets of postsynaptic neurons. Here, we describe the first application of a novel viral tracer, based on vesicular stomatitis virus (VSV), which directs retrograde transsynaptic viral spread between defined cell types. We use this virus in the mouse retina to show connectivity between starburst amacrine cells (SACs) and their known synaptic partners, direction-selective retinal ganglion cells, as well as to discover previously unknown connectivity between SACs and other retinal ganglion cell types. These novel connections were confirmed using physiological recordings. VSV transsynaptic tracing enables cell type-specific dissection of neural circuitry and can reveal synaptic relationships among neurons that are otherwise obscured due to the complexity and density of neuropil.
神经病毒作为突触前追踪剂的使用最早于 20 世纪 60 年代被描述,但直到最近,这些病毒才作为标记神经回路的方法变得流行起来。逆行单突触追踪载体的发展使我们能够可视化特定的突触后神经元上的突触前来源。在这里,我们描述了一种新型病毒示踪剂的首次应用,该示踪剂基于水疱性口炎病毒(VSV),可在特定细胞类型之间引导逆行突触间病毒传播。我们在小鼠视网膜中使用这种病毒来显示星爆型无长突细胞(SAC)与其已知的突触伙伴,即方向选择性视网膜神经节细胞之间的连接,以及发现 SAC 与其他视网膜神经节细胞类型之间以前未知的连接。这些新的连接通过生理记录得到了证实。VSV 突触前追踪能够特异性地解析神经回路,并能够揭示神经元之间的突触关系,否则由于神经胶的复杂性和密度,这些关系会被掩盖。