Program in Neuroscience.
Department of Psychology.
J Neurosci. 2019 Feb 13;39(7):1206-1221. doi: 10.1523/JNEUROSCI.1036-18.2018. Epub 2018 Dec 12.
Song learning in zebra finches () requires exposure to the song of a tutor, resulting in an auditory memory. This memory is the foundation for later sensorimotor learning, resulting in the production of a copy of the tutor's song. The cortical premotor nucleus HVC (proper name) is necessary for auditory and sensorimotor learning as well as the eventual production of adult song. We recently discovered that the intrinsic physiology of HVC neurons changes across stages of song learning, but are those changes the result of learning or are they experience-independent developmental changes? To test the role of auditory experience in driving intrinsic changes, patch-clamp experiments were performed comparing HVC neurons in juvenile birds with varying amounts of tutor exposure. The intrinsic physiology of HVC neurons changed as a function of tutor exposure. Counterintuitively, tutor deprivation resulted in juvenile HVC neurons showing an adult-like phenotype not present in tutor-exposed juveniles. Biophysical models were developed to predict which ion channels were modulated by experience. The models indicate that tutor exposure transiently suppressed the and T-type Ca currents in HVC neurons that target the basal ganglia, whereas tutor exposure increased the resting membrane potential and decreased the spike amplitude in HVC neurons that drive singing. Our findings suggest that intrinsic plasticity may be part of the mechanism for auditory learning in the HVC. More broadly, models of learning and memory should consider intrinsic plasticity as a possible mechanism by which the nervous system encodes the lasting effects of experience. It is well established that learning involves plasticity of the synapses between neurons. However, the activity of a neural circuit can also be dramatically altered by changes in the intrinsic properties (ion channels) of the component neurons. The present experiments show experience-dependent changes in the intrinsic physiology of neurons in the cortical premotor nucleus HVC (proper name) in juvenile zebra finches () during auditory learning of a tutor's song. Tutor deprivation does not "arrest" development of intrinsic properties, but rather results in neurons with a premature adult-like physiological phenotype. It is possible that auditory learning involves a form of nonsynaptic plasticity and that experience-dependent suppression of specific ion channels may work in concert with synaptic plasticity to promote vocal learning.
在斑胸草雀中,歌曲学习需要暴露于导师的歌声中,从而产生听觉记忆。这种记忆是后来进行感觉运动学习的基础,导致产生导师歌曲的副本。皮质前运动核 HVC(正式名称)对于听觉和感觉运动学习以及最终产生成年歌曲都是必要的。我们最近发现,HVC 神经元的内在生理学在歌曲学习的各个阶段都会发生变化,但这些变化是学习的结果还是与学习无关的发育变化?为了测试听觉体验在驱动内在变化中的作用,我们进行了膜片钳实验,比较了具有不同导师暴露量的幼年鸟类的 HVC 神经元。HVC 神经元的内在生理学随导师暴露而变化。反直觉的是,导师剥夺导致幼年 HVC 神经元表现出一种成年样表型,而这种表型在导师暴露的幼年鸟类中不存在。生物物理模型被开发出来以预测哪些离子通道受经验调节。模型表明,导师暴露会短暂抑制靶向基底神经节的 HVC 神经元中的 和 T 型钙电流,而导师暴露会增加 HVC 神经元的静息膜电位并降低驱动歌唱的 HVC 神经元的尖峰幅度。我们的发现表明,内在可塑性可能是 HVC 中听觉学习的机制之一。更广泛地说,学习和记忆模型应该将内在可塑性视为神经系统编码经验持久影响的一种可能机制。学习涉及神经元之间突触的可塑性已经得到充分证实。然而,神经元的活动也可以通过组成神经元的内在特性(离子通道)的变化而显著改变。目前的实验表明,在幼年斑胸草雀的听觉学习导师歌曲期间,皮质前运动核 HVC(正式名称)中的神经元的内在生理学发生了经验依赖性变化。导师剥夺并没有“阻止”内在特性的发展,而是导致具有过早的成年样生理表型的神经元。听觉学习可能涉及一种非突触可塑性形式,并且特定离子通道的经验依赖性抑制可能与突触可塑性协同作用,以促进发声学习。