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Inhibition gates supralinear Ca2+ signaling in Purkinje cell dendrites during practiced movements

机译:练习运动过程中浦肯野细胞树突中超线性Ca2 +信号的抑制门

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摘要

Motor learning involves neural circuit modifications in the cerebellar cortex, likely through re-weighting of parallel fiber inputs onto Purkinje cells (PCs). Climbing fibers instruct these synaptic modifications when they excite PCs in conjunction with parallel fiber activity, a pairing that enhances climbing fiber-evoked Ca2+ signaling in PC dendrites. In vivo, climbing fibers spike continuously, including during movements when parallel fibers are simultaneously conveying sensorimotor information to PCs. Whether parallel fiber activity enhances climbing fiber Ca2+ signaling during motor behaviors is unknown. In mice, we found that inhibitory molecular layer interneurons (MLIs), activated by parallel fibers during practiced movements, suppressed parallel fiber enhancement of climbing fiber Ca2+ signaling in PCs. Similar results were obtained in acute slices for brief parallel fiber stimuli. Interestingly, more prolonged parallel fiber excitation revealed latent supralinear Ca2+ signaling. Therefore, the balance of parallel fiber and MLI input onto PCs regulates concomitant climbing fiber Ca2+ signaling.
机译:运动学习涉及小脑皮质的神经回路改变,可能是通过将平行纤维输入重新加权到浦肯野细胞(PC)上来实现的。攀登纤维在刺激PC时会提示这些突触修饰,并具有平行的纤维活性,这种配对可增强PC树突中攀登纤维诱发的Ca 2 + 信号传导。在体内,攀爬纤维会连续不断地运动,包括在平行纤维同时向PC传递感觉运动信息的运动过程中。在运动行为过程中,平行纤维的活性是否会增强攀登纤维的Ca 2 + 信号尚不清楚。在小鼠中,我们发现在练习运动过程中平行纤维激活的抑制性分子层中间神经元(MLIs)抑制了PC中攀登纤维Ca 2 + 信号的平行纤维增强。对于短暂的平行纤维刺激,在急性切片中获得了相似的结果。有趣的是,更长的平行纤维激发显示出潜在的超线性Ca 2 + 信号。因此,并行光纤和输入到PC上的MLI的平衡会调节伴随的攀爬光纤Ca 2 + 信号。

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