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Development of an Acute Method to Deliver Transgenes Into the Brains of Adult Xenopus laevis

机译:一种将转基因传递到成年非洲爪蟾大脑中的急性方法的开发

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摘要

The central vocal pathway of the African clawed frog, Xenopus laevis, is a powerful vertebrate model to understand mechanisms underlying central pattern generation. However, fast and efficient methods of introducing exogenous genes into the neurons of adult X. laevis are currently not available. Here, we systematically tested methods of transgene delivery into adult X. laevis neurons. Although successfully used for tadpole neurons for over a decade, electroporation was not efficient in transfecting adult neurons. Similarly, adeno-associated virus (AAV) was not reliable, and lentivirus (LV) failed to function as viral vector in adult Xenopus neurons. In contrast, vesicular stomatitis virus (VSV) was a fast and robust vector for adult X. laevis neurons. Although toxic to the host cells, VSV appears to be less virulent to frog neurons than they are to mice neurons. At a single cell level, infected neurons showed normal physiological properties up to 7 days post infection and vocal circuits that included infected neurons generated normal fictive vocalizations up to 9 days post infection. The relatively long time window during which the physiology of VSV-infected neurons can be studied presents an ideal condition for the use of optogenetic tools. We showed that VSV does not gain entry into myelinated axons, but is taken up by both the soma and axon terminal; this is an attractive feature that drives transgene expression in projection neurons. Previous studies showed that VSVs can spread across synapses in anterograde or retrograde directions depending on the types of glycoprotein that are encoded. However, rVSV did not spread across synapses in the Xenopus central nervous system. The successful use of VSV as a transgene vector in amphibian brains not only allows us to exploit the full potential of the genetic tools to answer questions central to understanding central pattern generation, but also opens the door to other research programs that focus on non-genetic model organisms to address unique questions.
机译:非洲爪蛙Xenopus laevis的中央发声途径是一种强大的脊椎动物模型,可用来理解产生中央模式的机制。但是,目前尚无将外源基因引入成年X.laevis的神经元的快速有效方法。在这里,我们系统地测试了将基因转入成人X. laevis神经元的方法。尽管成功地将t用于神经元已有十多年了,但电穿孔在转染成年神经元方面并不有效。同样,腺相关病毒(AAV)也不可靠,慢病毒(LV)在成年非洲爪蟾神经元中不能作为病毒载体起作用。相比之下,水泡性口炎病毒(VSV)是成人X.laevis神经元的快速而强大的载体。尽管对宿主细胞有毒,但VSV对青蛙神经元的毒性似乎不如对小鼠神经元的毒性。在单个细胞水平上,被感染的神经元在感染后长达7天显示出正常的生理特性,包括被感染的神经元在内的声带在感染后长达9天产生了虚构的正常发声。可以研究VSV感染的神经元的生理学的相对较长的时间窗为使用光遗传学工具提供了理想的条件。我们表明,VSV不会进入有髓的轴突,但会被体细胞和轴突末端吸收。这是一个驱动投影神经元中转基因表达的诱人特征。先前的研究表明,VSV可以根据编码糖蛋白的类型在顺行或逆行方向上跨突触传播。但是,rVSV并未在非洲爪蟾中枢神经系统的突触中传播。 VSV作为两栖动物大脑中的转基因载体的成功使用,不仅使我们能够利用遗传工具的全部潜力来回答理解中央模式产生的核心问题,而且还为其他专注于非遗传的研究计划打开了大门模拟生物以解决独特的问题。

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