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Optogenetic tools for in vivo applications in neonatal mice

机译:用于新生儿小鼠的体内应用的致光学工具

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Spontaneous neural activities exist early in development and their spatiotemporal patterns play important roles in the development of sensory maps such as maps of retinotopy in the visual system. We summarized different optogenetic tools, including transgenic mouse lines, viral-mediated transfection and electroporation methods to enable the expression of light-gated channelrhodopsin (ChR2) in retinal ganglion cells (RGCs) before the onset of vision. Patch-clamp and extracellular recording experiments verified that activities of ChR2-expressing cells were precisely manipulated by the patterns of optical stimuli. In chronic stimulation experiments, light-emitting diodes controlled the activity patterns of ChR2-expressing RGCs in vivo. Changes in the retinotopic map in Superior Colliculus (SC) were examined by quantifying the relative sizes of fluorescently labeled target zones. Our results revealed that various optogenetic and optical tools can manipulate retinal activities with precise temporal patterns. These techniques can be readily used in studying the development of the central nervous system of neonatal rodents.
机译:早期发展的自发性神经活动,它们的时空模式在开发感官地图中发挥重要作用,例如视觉系统中视网膜的地图。我们总结了不同的致敏工具,包括转基因小鼠线,病毒介导的转染和电穿孔方法,以使视网膜神经节细胞(RGCs)中的光门控通道豆荚(CHR2)的表达能够在发生前发作。贴片钳和细胞外记录实验证实,通过光学刺激的模式精确地操纵CHR2表达细胞的活性。在慢性刺激实验中,发光二极管控制了体内CHR2表达RGC的活性模式。通过量化荧光标记的目标区的相对尺寸来检查高级小集体(SC)中的视网膜运动地图的变化。我们的研究结果表明,各种光源和光学工具可以用精确的时间模式操纵视网膜活动。这些技术可以容易地用于研究新生儿啮齿动物的中枢神经系统的发展。

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