Raccuglia Davide, Mueller Uli
Department 8.3 Biosciences, Zoology/Physiology-Neurobiology, ZHMB (Center of Human and Molecular Biology), Natural Science and Technology III, Saarland University, D-66041 Saarbrücken, Germany.
Department 8.3 Biosciences, Zoology/Physiology-Neurobiology, ZHMB (Center of Human and Molecular Biology), Natural Science and Technology III, Saarland University, D-66041 Saarbrücken, Germany
J Neurosci. 2014 Nov 26;34(48):16086-92. doi: 10.1523/JNEUROSCI.0714-14.2014.
GABAergic modulation of neuronal activity plays a crucial role in physiological processes including learning and memory in both insects and mammals. During olfactory learning in honeybees (Apis mellifera) and Drosophila melanogaster the temporal relation between excitatory cholinergic and inhibitory GABAergic inputs critically affects learning. However, the cellular mechanisms of temporal integration of these antagonistic inputs are unknown. To address this question, we use calcium imaging of isolated honeybee and Drosophila Kenyon cells (KCs), which are targets of cholinergic and GABAergic inputs during olfactory learning. In the whole population of honeybee KCs we find that pairing of acetylcholine (ACh) and γ-aminobutyric acid (GABA) Comment: Please use the greek letter for gamma reduces the ACh-induced calcium influx, and depending on their temporal sequence, induces different forms of neuronal plasticity. After ACh-GABA pairing the calcium influx of a subsequent excitatory stimulus is increased, while GABA-ACh pairing affects the decay time leading to elevated calcium levels during the late phase of a subsequent excitatory stimulus. In an exactly defined subset of Drosophila KCs implicated in learning we find similar pairing-specific differences. Specifically the GABA-ACh pairing splits the KCs in two functional subgroups: one is only weakly inhibited by GABA and shows no neuronal plasticity and the other subgroup is strongly inhibited by GABA and shows elevated calcium levels during the late phase of a subsequent excitatory stimulus. Our findings provide evidence that insect KCs are capable of contributing to temporal processing of cholinergic and GABAergic inputs, which provides a neuronal mechanism of the differential temporal role of GABAergic inhibition during learning.
GABA能对神经元活动的调节在包括昆虫和哺乳动物的学习与记忆等生理过程中起着至关重要的作用。在蜜蜂(西方蜜蜂)和黑腹果蝇的嗅觉学习过程中,兴奋性胆碱能输入和抑制性GABA能输入之间的时间关系对学习有着关键影响。然而,这些拮抗输入的时间整合的细胞机制尚不清楚。为了解决这个问题,我们对分离出的蜜蜂和果蝇的肯扬细胞(KC)进行钙成像,这些细胞是嗅觉学习过程中胆碱能和GABA能输入的靶细胞。在整个蜜蜂KC群体中,我们发现乙酰胆碱(ACh)和γ-氨基丁酸(GABA)(注释:请使用希腊字母表示γ)的配对会减少ACh诱导的钙内流,并且根据它们的时间顺序,会诱导不同形式的神经元可塑性。ACh-GABA配对后,随后兴奋性刺激的钙内流增加,而GABA-ACh配对则影响衰减时间,导致在随后兴奋性刺激的后期钙水平升高。在与学习相关的果蝇KC的一个精确界定的子集中,我们发现了类似的配对特异性差异。具体而言,GABA-ACh配对将KC分为两个功能亚组:一个亚组仅受到GABA的微弱抑制,且不表现出神经元可塑性,另一个亚组受到GABA的强烈抑制,并且在随后兴奋性刺激的后期显示出升高的钙水平。我们的研究结果提供了证据,表明昆虫KC能够参与胆碱能和GABA能输入的时间处理,这为学习过程中GABA能抑制的不同时间作用提供了一种神经元机制。