首页> 美国卫生研究院文献>Frontiers in Neuroanatomy >Dual Transneuronal Tracing in the Rat Entorhinal-Hippocampal Circuit by Intracerebral Injection of Recombinant Rabies Virus Vectors
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Dual Transneuronal Tracing in the Rat Entorhinal-Hippocampal Circuit by Intracerebral Injection of Recombinant Rabies Virus Vectors

机译:脑内注射重组狂犬病病毒载体在大鼠内脏-海马回路中的双重跨神经元示踪

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摘要

Dual transneuronal tracing is a novel viral tracing methodology which employs two recombinant viruses, each expressing a different reporter protein. Peripheral injection of recombinant pseudorabies viruses has been used as a powerful method to define neurons that coordinate outputs to various peripheral targets of motor and autonomic systems. Here, we assessed the feasibility of recombinants of rabies virus (RV) vector for dual transneuronal tracing in the central nervous system. First, we examined whether two different RV-vectors can double label cells in vitro, and showed that efficient double labeling can be realized by infecting targeted cells with the two RV-vectors within a short time interval. The potential of dual transneuronal tracing was then examined in vivo in the entorhinal-hippocampal circuit, using the chain of projections from CA3 pyramidal cells to CA1 pyramidal cells and subsequently to entorhinal cortex. Six days after the injection of two RV-vectors into the left and right entorhinal cortex respectively, double-labeled neurons were observed in CA3 bilaterally. Some double-labeled neurons showed a Golgi-like labeling. Dual transneuronal tracing potentially provides a powerful and sensitive method to study issues such as the amount of convergence and divergence within and between circuits in the central nervous system. Using this sensitive technique, we established that single neurons in CA3 are connected to the entorhinal cortex bilaterally with only one synaptic relay.
机译:双跨神经元示踪是一种新颖的病毒示踪方法,它采用两种重组病毒,每种病毒表达不同的报道蛋白。重组伪狂犬病病毒的外周注射已被用作定义神经元的有力方法,这些神经元可协调输出到运动和自主系统的各种外周靶标。在这里,我们评估了狂犬病毒(RV)载体重组体在中枢神经系统中进行双跨神经元示踪的可行性。首先,我们检查了两种不同的RV载体是否可以在体外对细胞进行双标记,并表明可以通过在短时间间隔内用两种RV载体感染靶细胞来实现有效的双标记。然后使用从CA3锥体细胞到CA1锥体细胞以及随后到内嗅皮层的投射链,在体内的内嗅海马回路中检查了双重跨神经元示踪的潜力。在分别向左右内嗅皮层注射两个RV载体六天后,双侧CA3中观察到了双标记神经元。一些双重标记的神经元显示出类似高尔基体的标记。双跨神经元描记法可能会提供一种强大而敏感的方法来研究诸如中枢神经系统内回路之间以及回路之间的收敛和发散量之类的问题。使用这种灵敏的技术,我们建立了CA3中的单个神经元仅通过一个突触中继器就被双边连接到内嗅皮层的问题。

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