Wolfson Institute for Biomedical Research and Department of Neuroscience, Physiology, and Pharmacology, University College London, Gower Street, London WC1E 6BT, UK.
Science. 2010 Sep 24;329(5999):1671-5. doi: 10.1126/science.1189664. Epub 2010 Aug 12.
The detection and discrimination of temporal sequences is fundamental to brain function and underlies perception, cognition, and motor output. By applying patterned, two-photon glutamate uncaging, we found that single dendrites of cortical pyramidal neurons exhibit sensitivity to the sequence of synaptic activation. This sensitivity is encoded by both local dendritic calcium signals and somatic depolarization, leading to sequence-selective spike output. The mechanism involves dendritic impedance gradients and nonlinear synaptic N-methyl-D-aspartate receptor activation and is generalizable to dendrites in different neuronal types. This enables discrimination of patterns delivered to a single dendrite, as well as patterns distributed randomly across the dendritic tree. Pyramidal cell dendrites can thus act as processing compartments for the detection of synaptic sequences, thereby implementing a fundamental cortical computation.
时间序列的检测和分辨是大脑功能的基础,它是感知、认知和运动输出的基础。通过应用模式化的双光子谷氨酸光解,我们发现皮质锥体神经元的单个树突对突触激活的序列表现出敏感性。这种敏感性由局部树突钙信号和体部去极化编码,导致序列选择性的尖峰输出。该机制涉及树突阻抗梯度和非线性突触 N-甲基-D-天冬氨酸受体激活,并且可推广到不同神经元类型的树突。这使得能够区分单个树突上传递的模式,以及随机分布在树突上的模式。因此,锥体神经元的树突可以作为检测突触序列的处理隔室,从而实现基本的皮质计算。