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. 2004 Jun 17;429(6993):761-6.
doi: 10.1038/nature02617. Epub 2004 Jun 9.

Structural basis of long-term potentiation in single dendritic spines

Masanori Matsuzaki  1 , Naoki Honkura, Graham C R Ellis-Davies, Haruo Kasai
Affiliations

Structural basis of long-term potentiation in single dendritic spines

Masanori Matsuzaki et al. Nature. .

Abstract

Dendritic spines of pyramidal neurons in the cerebral cortex undergo activity-dependent structural remodelling that has been proposed to be a cellular basis of learning and memory. How structural remodelling supports synaptic plasticity, such as long-term potentiation, and whether such plasticity is input-specific at the level of the individual spine has remained unknown. We investigated the structural basis of long-term potentiation using two-photon photolysis of caged glutamate at single spines of hippocampal CA1 pyramidal neurons. Here we show that repetitive quantum-like photorelease (uncaging) of glutamate induces a rapid and selective enlargement of stimulated spines that is transient in large mushroom spines but persistent in small spines. Spine enlargement is associated with an increase in AMPA-receptor-mediated currents at the stimulated synapse and is dependent on NMDA receptors, calmodulin and actin polymerization. Long-lasting spine enlargement also requires Ca2+/calmodulin-dependent protein kinase II. Our results thus indicate that spines individually follow Hebb's postulate for learning. They further suggest that small spines are preferential sites for long-term potentiation induction, whereas large spines might represent physical traces of long-term memory.

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Conflict of interest statement

Competing interests statement The authors declare that they have no competing financial interests.

Figures

Figure 1
Figure 1
Spine-head enlargement induced by repetitive uncaging of MNI-glutamate. a, Time-lapse images of dendritic spines on a hippocampal CA1 pyramidal neuron expressing eGFP. The arrowhead indicates the spot of two-photon uncaging of MNI-glutamate, which was achieved by stimulation for 1 min at 1 Hz, beginning at time zero in a bathing solution lacking Mg. Images were stacked along the z axis. Scale bar, 1 μm. b, Time course of spine-head volume, estimated from stacked images, of the stimulated (black circles) and neighbouring (green diamonds) spines shown in a. c, Time-lapse images of a spine on a dendrite that was affected by electrical stimulation of presynaptic fibres at 2 Hz for 1 min; d, time course of the head volume. e, Fluorescence intensity along a line crossing the centre of the stimulated spine head shown in a at −3 min (black circles) and 81 min (red circles). Smooth black and red lines represent the predictions made for the z-stacked images of spheres with diameters of 0.46 and 0.59 μm, respectively (see Supplementary Methods). The dashed line is scaled from the smooth black one. f, h, Averaged time courses of spine-head volume for two-photon uncaging of MNI-glutamate (circles, n = 40), neighbouring spines (green diamonds in h, n = 34), 2-Hz electrical stimulation in the absence of Mg (blue open triangles, n = 19) or 100 Hz electrical stimulation in the presence of Mg (blue closed triangles, n = 14). Error bars represent +/− s.e.m. g, Initial time course of spine fluorescence. The intensity in a single plane drawn through the centre of the spines was sampled; the average for 11 spines is shown. Dotted lines show time courses corresponding to the mean +/− s.d., and the horizontal bar indicates the period of repetitive uncaging.
Figure 2
Figure 2
Properties of the spine-head enlargement. a, c, Averaged time course (+/− s.e.m.) of spine-head volume for large (a) and small (c) spines with an initial head volume of > 0.1 μm3 (n = 20) and < 0.1 μm3 (n = 20), respectively. ΔV transient represents the difference in spine-head volume between 1–5 and 70–100 min after stimulation, whereas ΔV long represents that between 70–100 min after and 0–20 min before stimulation. b, Example of an enlargement of a large spine. The arrowhead indicates the point of two-photon uncaging of MNI-glutamate. d, Mean values of ΔV transient and DV long for small and large spines (n = 20 each). e, Effects of 50 μM AP5 or 4 μM KN62 on the averaged time course (+/− s.e.m.) of spine-head volume for small spines. f, Pharmacological properties of the transient and long-lasting phases of head enlargement in small spines. Antagonists examined were 1 mM MCPG (n = 15), 50 μM AP5 (n = 7), 20 μM W7 (n = 11), 4 μM KN62 (n = 12) and 20 nM (n = 12) or 100 nM latrunculin A (n = 7). *P < 0.05, **P < 0.01 (Mann–Whitney U test). Errors bars in d and f show s.e.m.
Figure 3
Figure 3
Colocalization of enlargement of spine heads and potentiation of AMPA- receptor-mediated currents. a, b, Examples of small spines that showed transient (a) or long-lasting (b) enlargement (upper panels) and potentiation of AMPA currents (lower panels). Three-dimensional mapping of AMPA currents was performed in neurons that were clamped in the perforated-patch mode. The amplitude of AMPA currents is pseudocolour coded and stacked along the z axis by the maximum-intensity method. The neurons were depolarized to 0 mV and the small spines, indicated by the arrowheads, were stimulated by two-photon uncaging of MNI-glutamate at 2 Hz between times 0 and 60 s. White lines in the lower panels indicate contours of dendrites. Scale bars, 1 μm. c, d, Examples of small (c) and large (d) spines whose heads failed to enlarge in response to paired stimulation.
Figure 4
Figure 4
Relationship between spine-head enlargement and potentiation of AMPA- receptor-mediated currents. a, Time courses (+/− s.e.m.) of spine-head volume (V, open symbols) and maximal AMPA currents (I, filled symbols) normalized to the original values. The data were derived from all the small spines (n = 9) that showed enlargement immediately after pairing stimulation and for which it was possible to obtain current maps more than 30 min after paired stimulation in the perforated-patch recording mode. Circles and diamonds represent stimulated and neighbouring spines, respectively. b, Relationships between normalized amplitudes of head enlargement (ΔV) and potentiation of AMPA currents (ΔCurrent) in the early phase (1–5 min after stimulation) and long- lasting phase (30–120 min) in small and large spines. The continuous and dashed lines are regression lines for the early and long-lasting phases, respectively; correlation coefficients are 0.72 (n = 24, P < 0.0001) and 0.95 (n = 9, P < 0.0001), respectively. The red and yellow crosses show data obtained in the presence of AP5 (n = 5) or with whole-cell recording (n = 7), respectively. Black and blue dotted lines are 0% and 30% levels, respectively.
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