Targeted intracellular voltage recordings from dendritic spines using quantum-dot-coated nanopipettes

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作者
Jayant K. [1 ,2 ,3 ,4 ]
Hirtz J.J. [2 ,3 ,4 ]
Plante I.J.-L. [5 ]
Tsai D.M. [1 ,2 ,3 ,4 ]
De Boer W.D.A.M. [2 ,3 ,4 ,5 ]
Semonche A. [2 ]
Peterka D.S. [2 ,3 ,4 ]
Owen J.S. [5 ]
Sahin O. [2 ,3 ]
Shepard K.L. [1 ,3 ,4 ,6 ]
Yuste R. [2 ,3 ,4 ]
机构
[1] Department of Electrical Engineering, Columbia University, New York, 10027, NY
[2] Department of Biological Sciences, Columbia University, New York, 10027, NY
[3] Neuro Technology Center, Columbia University, New York, 10027, NY
[4] Kavli Institute of Brain Science, Columbia University, New York, 10027, NY
[5] Department of Chemistry, Columbia University, New York, 10027, NY
[6] Department of Biomedical Engineering, New York, 10027, NY
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D O I
10.1038/nnano.2016.268
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摘要
Dendritic spines are the primary site of excitatory synaptic input onto neurons, and are biochemically isolated from the parent dendritic shaft by their thin neck. However, due to the lack of direct electrical recordings from spines, the influence that the neck resistance has on synaptic transmission, and the extent to which spines compartmentalize voltage, specifically excitatory postsynaptic potentials, albeit critical, remains controversial. Here, we use quantum-dot-coated nanopipette electrodes (tip diameters ~15-30 nm) to establish the first intracellular recordings from targeted spine heads under two-photon visualization. Using simultaneous somato-spine electrical recordings, we find that back propagating action potentials fully invade spines, that excitatory postsynaptic potentials are large in the spine head (mean 26 mV) but are strongly attenuated at the soma (0.5-1 mV) and that the estimated neck resistance (mean 420 M & Omega;) is large enough to generate significant voltage compartmentalization. Nanopipettes can thus be used to electrically probe biological nanostructures. © 2017 Macmillan Publishers Limited, part of Springer Nature.
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页码:335 / 342
页数:7
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