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Metabotropic glutamate receptors activate dendritic calcium waves and TRPM channels which drive rhythmic respiratory patterns in mice

机译:代谢型谷氨酸受体激活树突状钙波和TRPM通道从而驱动小鼠的节律性呼吸模式

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摘要

Respiration in vertebrates is generated by a compact network which is located in the lower brainstem but cellular mechanisms which underlie persistent oscillatory activity of the respiratory network are yet unknown. Using two-photon imaging and patch-clamp recordings in functional brainstem preparations of mice containing pre-Bötzinger complex (preBötC), we examined the actions of metabotropic glutamate receptors (mGluR1/5) on the respiratory patterns. The agonist DHPG potentiated and antagonist depressed respiration-related activities. In the inspiratory neurons, we observed rhythmic activation of non-selective channels which had a conductance of 24 pS. Their activity was enhanced with membrane depolarization and after elevation of calcium from the cytoplasmic side of the membrane. They were activated by a non-hydrolysable PIP2 analogue and blocked by flufenamate, ATP4− and Gd3+. All these properties correspond well to those of TRPM4 channels. Calcium imaging of functional slices revealed rhythmic transients in small clusters of neurons present in a network. Calcium transients in the soma were preceded by the waves in dendrites which were dependent on mGluR activation. Initiation and propagation of waves required calcium influx and calcium release from internal stores. Calcium waves activated TPRM4-like channels in the soma and promoted generation of inspiratory bursts. Simulations of activity of neurons communicated via dendritic calcium waves showed emerging activity within neuronal clusters and its synchronization between the clusters. The experimental and theoretical data provide a subcellular basis for a recently proposed group-pacemaker hypothesis and describe a novel mechanism of rhythm generation in neuronal networks.
机译:脊椎动物的呼吸作用是由位于下脑干的紧凑网络产生的,但仍不清楚呼吸网络持续振荡活动基础的细胞机制。使用双光子成像和膜片钳记录功能的小鼠包含前玻耳琴格复合体(preBötC)的功能性脑干中,我们检查了代谢型谷氨酸受体(mGluR1 / 5)对呼吸模式的作用。 DHPG激动剂可增强和拮抗呼吸相关的活性。在吸气神经元中,我们观察到电导率为24 pS的非选择性通道的节律性激活。膜去极化和钙从膜细胞质侧升高后,它们的活性得以增强。它们被不可水解的PIP2类似物激活,并被氟丁酸,ATP 4-和Gd 3 + 阻断。所有这些属性都很好地对应于TRPM4通道。功能切片的钙成像显示网络中存在的神经元小簇的节律性瞬变。钙在钙离子中的瞬变先于树突状波,其依赖于mGluR激活。波浪的产生和传播需要钙的涌入和钙从内部储存中释放出来。钙波激活了躯体中类似TPRM4的通道,并促进了吸气爆发的产生。通过树突状钙波交流的神经元活动的模拟显示神经元簇内出现的活动及其在簇之间的同步。实验和理论数据为最近提出的群-起搏器假说提供了亚细胞基础,并描述了神经元网络中产生节奏的新机制。

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