Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines
© Matsuzaki et al; licensee BioMed Central Ltd. 2011
Received: 13 April 2010
Accepted: 7 July 2010
Published: 26 January 2011
Dendritic spines of pyramidal neurons are distributed along the complicated structure of the dendritic branches and possess a variety of morphologies associated with synaptic strength. The location and structure of dendritic spines determine the extent of synaptic input integration in the postsynaptic neuron. However, how spine location or size relates to the position of innervating presynaptic cells is not yet known. This report describes a new method that represents a first step toward addressing this issue.
The technique combines two-photon uncaging of glutamate over a broad area (~500 × 250 × 100 μm) with two-photon calcium imaging in a narrow region (~50 × 10 × 1 μm). The former was used for systematic activation of layer 2/3 pyramidal cells in the rat motor cortex, while the latter was used to detect the dendritic spines of layer 5 pyramidal cells that were innervated by some of the photoactivated cells. This technique allowed identification of various sizes of innervated spine located <140 μm laterally from the postsynaptic soma. Spines distal to their parent soma were preferentially innervated by cells on the ipsilateral side. No cluster of neurons innervating the same dendritic branch was detected.
This new method will be a powerful tool for clarifying the microarchitecture of synaptic connections, including the positional and structural characteristics of dendritic spines along the dendrites.
The microarchitecture of synaptic connections determines information processing in cortical circuits. The inter/intra-layer and inter/intra-columnar architecture of synaptic connectivity has been revealed by laser-scanning one- or two-photon stimulation of neurons with caged glutamate [1–7]. Although previous experiments have measured the amplitude of postsynaptic currents or depolarization, they have not been able to identify the sites of synaptic connections.
The structure and location of dendritic spines, the major postsynaptic sites of excitatory synapses, are crucial to information integration in the postsynaptic cell . Spine size correlates well with the number of functional α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic (AMPA) receptors [9–11]. Dendritic spine location determines the extent to which depolarization spreads into the soma, the local dendritic spike, and synaptic plasticity [12, 13]. Induction of nonlinear depolarization had been suggested to require the activation of dozens of dendritic spines along the same dendritic tree within a narrow time window (~6 ms) [14, 15]. Functionally or spatially associated pyramidal cells innervating the same dendritic branch of a postsynaptic cell may cause correlated activation in the brain. In order to examine this possibility, the location of presynaptic cells and the size and location of the dendritic spines that they innervate must be determined.
Although it is possible to determine the structure and location of synaptic connectivity by staining pair-recorded cells, it is very difficult to identify pairs of connecting cells over a relatively broad area and then find their synaptic sites [16–19]. In this study, we developed a new method that combines calcium (Ca2+) imaging with photostimulation via two-photon macro photolysis of caged glutamate (2pMAPG) . The volume of uncaged glutamate is restricted to the focal volume of the laser beam. Thus, it is possible to map the approximate positions of photostimulated cells that induce postsynaptic currents in a patch-clamped cell via three-dimensional (3D) scanning of laser focal volumes from 2pMAPG in slices of rat cortex . During 2pMAPG mapping in layer 2/3, we also performed Ca2+ imaging in the dendrites of layer 5 pyramidal cells and identified dendritic spines in which photostimulated cells triggered 2pMAPG-mediated Ca2+ transients. We found that spines located distal to their parent soma were innervated preferentially by cells on the ipsilateral side.
Activation of layer 2/3 pyramidal cells with 2pMAPG mapping
First, the 3D 2pMAPG mapping of induced action potentials (APs) was validated in layer 2/3 pyramidal cells in the rat motor cortex. In order to activate a large number of glutamate receptors to induce APs, the focal volume for 2pMAPG was expanded with a 720-nm laser beam . The point-spread function of the focal volume for 2pMAPG was estimated using 0.1-μm fluorescent beads at lateral and axial full-width at half-maximum values (FWHMs) of 1.03 ± 0.04 μm and 15.4 ± 0.7 μm (n = 11), respectively. These lateral and axial FWHMs were 3.8- and 9.8-fold longer, respectively, than those for two-photon imaging using the 830-nm laser beam (see Methods). Therefore, the 2pMAPG volume was approximately 140-fold larger (3.8 × 3.8 × 9.8) than that obtained by two-photon imaging.
We examined whether the 3D center of the stimulated cell soma could be predicted from the positions of AP-evoking pixels. Comparison of the center of the soma and the average position of the AP-evoking pixels indicated only slight positional differences (-12 ± 12 μm along the X-axis, -4 ± 7 μm along the Y-axis, and 11 ± 7 μm along the Z-axis) using the XYZ axes indicated in Figure 1C (n = 8 cells). Thus, the average position of AP-evoking pixels predicted the position of the stimulated neuron soma with errors of no more than 12 μm in each direction.
Identification of dendritic spines innervated by electrically-stimulated axons
Next, electrical stimulation of presynaptic axons was used to examine the reliability of Ca2+ imaging for the detection of Ca2+ transients in dendritic spines. Recoded layer 5 pyramidal cells were filled with Ca2+ indicator (750 μM Fluo-5F; green fluorescence, G) and fluorescent dye (45 μM Alexa Fluor 594; red fluorescence, R). An 830-nm laser beam was used to perform Ca2+ imaging. The Ca2+ imaging regions were approximately 40 × 10 μm in area and included 17 to 31 dendritic spines on each layer 5 pyramidal cell. The acquisition time per imaging frame was 170-320 ms. A stimulation pipette was inserted near the selected dendrite (eight dendritic regions in five cells). Axons adjacent to the dendrite were stimulated 10 to 20 times at 0.2-0.25 Hz during sequential Ca2+ imaging. The membrane potential was held at -30 mV to relieve the Mg2+ block of N-methyl-D-aspartate receptors (NMDARs). The difference between the ratios of G intensity and R intensity (G/R) immediately after and immediately before stimulation, ΔG/Rtransient, was divided by the mean G/R before stimulation (G/Rbase) in the same spine. This ratio was defined as the amplitude of a Ca2+ transient. Ca2+ transients with amplitudes >1 were detected clearly in some spines immediately after a single electrical stimulation of presynaptic axons (Figure 1D-F). Ca2+ transients were not caused by direct electrical stimulation of the observed dendrite, since neither a large inward current with a long decay time nor a widespread rise in Ca2+ transient were observed in the dendritic shaft (Figure 1D). The success rate of Ca2+ transients (1 - failure rate of occurrence of Ca2+ transients) was 0.65 ± 0.08 (n = 11 spines from five cells), which probably reflected the reliability of glutamate release. However, as this value might also reflect the failure rate for induction of the axonal AP, it is not discussed here. In successful trials, the amplitude of Ca2+ transients correlated inversely with spine size (Figure 1G; r = -0.66, P < 0.01, Spearman's rank correlation), consistent with previous results in hippocampal cells . Although ΔG/Rtransient increased with decreasing spine size, the amplitude of Ca2+ transients were >fivefold larger than the coefficient of variance (CV) of G/Rbase in the same spine, regardless of spine size (Figure 1G; P < 0.001, paired t test). Thus, we concluded that Ca2+ transients could be reliably detected in spines of various sizes under the experimental conditions used here.
Development of simultaneous 2pMAPG mapping and Ca2+imaging
Reliable measurement of the amplitude or number of excitatory postsynaptic currents (EPSCs) induced by 2pMAPG could not be achieved due to the following experimental side-effects. First, axial movement of the objective caused electric artifacts that continued for >50 ms after the end of 2pMAPG in the whole-cell current measurement (Additional File 1: Figure S1G). Second, since the holding potential was maintained at -30 mV, the driving force of the cation influx was weaker than at -70 mV and the amplitudes of unitary EPSCs were relatively small (<10 pA). Thus, only Ca2+ transients could be considered as synaptic inputs unless otherwise noted.
Identification of dendritic spines on a layer 5 pyramidal cell innervated by layer 2/3 pyramidal cells
During 2pMAPG mapping, Ca2+ transients were detected in one to three dendritic spines in the first or second imaging frame after 2pMAPG (Figure 3B to 3D). These Ca2+ transients were specific to individual spines and could be distinguished from global Ca2+ increases arising from dendritic spikes possibly triggered by bursting activity (Figure 3E). Following reconstruction of the pixels for 2pMPAG, which were assumed to induce Ca2+ transients, it became apparent that these pixels were frequently attached to each other laterally or axially within the 3D mapping region (yellow pixels in Figure 3A). This finding strongly suggests that one of the neurons associated with these pixels innervated the dendritic spine exhibiting Ca2+ transients, since most AP-evoking pixels (59/63 pixels in eight cells) possessed neighbouring AP-evoking pixels when layer 2/3 pyramidal cells were stimulated by 2pMAPG mapping. However, Ca2+ transients were also detected occasionally in a dendritic spine immediately after 2PMAPG at a given pixel, even though neighboring pixels showed no Ca2+ transient associated with 2pMAPG. These Ca2+ transients might occur spontaneously in a dendritic spine. In order to avoid such contamination, Ca2+ transients were considered to be induced by 2pMAPG when they occurred immediately after 2pMAPGs in at least two neighbouring pixels within a distance of less than 65 μm (approximately the length of two pixels; Additional File 2: Figure S2). These pixels are referred to as grouped Ca2+ transient-evoking pixels (Additional File 2: Figure S2).
For further determination of the reliability of 2pMAPG-induced Ca2+ transients, 2pMAPG was performed repeatedly at one of the grouped Ca2+ transient-evoking pixels with fast Ca2+ imaging (n = 4 spines in three cells). Figure 3F-H shows representative Ca2+ transients from one of these spines. The mean success rate in 10 trials was 0.95 ± 0.03 (n = 4 spines). If the laser intensity for 2pMAPG was reduced, neither Ca2+ transients nor putative postsynaptic currents were evoked (Additional File 3: Figure S3). These findings indicate that 2pMAPG reliably triggered Ca2+ transients in the spines, and they were not evoked by unrelated, spontaneous glutamate release from presynaptic boutons.
Convergence of synaptic inputs on the same dendritic branch
In the remaining 19 pairs of dendritic spines, Ca2+ transients were induced by 2pMAPG at different grouped Ca2+ transient-evoking pixels, which suggests that these spines were innervated by different presynaptic neurons. Ten pairs of spines were located on the same dendritic branches, at mean distances of 18 ± 4 μm (2-37 μm). An example is shown in Figure 5C. Nine pairs were located on different dendritic branches of the same postsynaptic cells.
The average position of the grouped Ca2+ transient-evoking pixels was used to predict the position of the presynaptic cells. In order to ascertain whether or not this determination was valid, we reexamined the data for AP induction of layer 2/3 pyramidal cells described in the first part of the Results. Using the same criteria as for the grouped Ca2+ transient-evoking pixels, AP-evoking pixels with neighbouring AP-evoking pixels are referred to as grouped AP-evoking pixels. The differences between the average position of the grouped AP-evoking pixels and the centre of the soma were -14 ± 16 μm along the X-axis, 5 ± 8 μm along the Y-axis, and 14 ± 7 μm along the Z-axis (n = 8 cells). Thus, the average position of grouped AP-evoking pixels represented the approximate position of the stimulated neuron soma. The number of grouped AP-evoking pixels per layer 2/3 cell was 7.4 ± 0.5 (n = 8 cells), which was more than the number of grouped Ca2+ transient-evoking pixels per spine (5.2 ± 0.5, n = 34 spines; P < 0.05, Mann-Whitney U test). This difference may be due to some AP-evoking pixels with a single AP failing to induce Ca2+ transients in the spine. Assuming that the distribution of grouped Ca2+ transient-evoking pixels was similar to that of grouped AP-evoking pixels, the average position of grouped Ca2+ transient-evoking pixels can be defined as the position of a presynaptic neuron innervating a dendritic spine showing Ca2+ transients.
The distances between the average positions of grouped Ca2+ transient-evoking pixels were calculated. No significant difference in distance from the somata was detected between spine pairs on the same dendritic branch and those on different dendritic branches (Figure 5D; 97 ± 18 μm, n = 10 pairs versus 104 ± 27 μm, n = 9 pairs, respectively; P = 0.87, Mann-Whitney U test). In addition, no more than two presynaptic neurons innervating the same dendritic branch within an imaging region could be detected in any 100-μm spherical area. Thus, despite the very small number of dendritic spines showing Ca2+ transients on the same dendritic branch, layer 2/3 presynaptic neurons innervating the same dendritic branch did not appear to be clustered more clearly or frequently than those innervating scattered spines.
Relationship between the structure and function of dendritic spines on layer 5 pyramidal cells
First, we examined the relationships between spine size and each of the positional parameters. Spine size did not correlate with xsp, which varied from 20 to 140 μm (r = 0.05, n = 34, P = 0.77; Spearman's rank coefficient). Spines were classified into four groups according to size (Figure 6B; spines of 0-0.1 μm3, n = 15; 0.1-0.2 μm3, n = 8; 0.2-0.3 μm3, n = 5 and >0.3 μm3, n = 6). The lateral distance between the postsynaptic and presynaptic somata , and the lateral distance between the dendritic spine and the presynaptic soma , were not significantly different across the four groups (Figure 6C; P = 0.68 and 0.39, respectively, one-way ANOVA). The straight-line distance of the dendritic spine from the presynaptic soma , was significantly longer in spines of 0-0.1 μm3 than in those of 0.1-0.2 μm3 (Figure 6C; P < 0.05, one-way ANOVA followed by Tukey's test). Presynaptic cells innervating spines of >0.2 μm3 were preferentially distributed in the field ipsilateral to the spine (nine of 11 cells; orange and red closed circles in Figure 6B). In fact, the xpre of spines >0.2 μm3 was significantly greater than that of spines <0.2 μm3 (Figure 6D; 83 ± 20 μm versus 3 ± 25 μm, respectively; P < 0.05, Mann-Whitney U test). However, no significant differences in xpre were detected between the four size groups (Figure 6D; P = 0.11, one-way ANOVA).
This study developed a novel method for simultaneously performing Ca2+ imaging in a narrow region that includes a segment of a dendrite, and 2pMAPG across a broad area that includes many pyramidal cells. The methodological focus was the simultaneous use of two two-photon lasers that over- and under-filled the back aperture of the objective for Ca2+ imaging of dendritic spines and photostimulation of neurons, respectively. It was important to inhibit vibration of the objective, which accompanied the rapid axial movement between the imaging plane and the photostimulation plane. This inhibition was achieved by attaching dampers to the objective. This novel method allowed identification of spines innervated by some of the systematically stimulated neurons over a relatively broad 3D area.
In contrast to a paired recording where the presynaptic cell is identified precisely, this method required prediction of the location of the presynaptic cell from the grouped Ca2+ transient-evoking pixels. The Ca2+ transient might be generated by a directly photostimulated presynaptic cell or by a presynaptic cell synaptically activated by multiple photostimulated neurons. To clarify this issue, we estimated the number of AP-evoking cells per 2pMAPG (NAPcell). According to our previous report,  NAPcell is estimated as NAPpixel × Vpixel × ρcell, where NAPpixel is the number of AP-evoking pixels per cell during 2pMAPG mapping, Vpixel is the volume of a single pixel for 2pMAPG, and ρcell is the density of excitatory pyramidal neurons. Assuming that NAPpixel, Vpixel, and ρcell in layer 2/3 were 7.9, 31 × 31 × 50 μm, and 6.8 × 10-5 μm-3 , respectively, the NAPcell in layer 2/3 was 26.
According to Holmgren et al.,  the connection probability between nearby (distance of <25 μm) layer 2/3 pyramidal neurons is 0.18, and the average amplitude of excitatory post-synaptic potentials (EPSPs) between connected pairs of neurons is 0.65 mV. Thus, if the APs induced in 26 nearby cells simultaneously depolarize a postsynaptic cell, its depolarization is estimated at 26 × 0.18 × 0.65 = 3 mV. Even if each of the stimulated cells generated three APs simultaneously, the total synaptic depolarization will be 9 mV, which is not large enough to generate an AP in the postsynaptic cell. In fact, at any 2pMAPG pixel that was not associated with the soma or proximal dendrites of the recorded cell, no AP was induced in a recorded layer 2/3 cell during 2pMAPG mapping. However, if 2pMAPG directly depolarized a cell near the stimulated pixel and its depolarization did not reach the threshold for generation of an AP, synaptic inputs from its nearby photostimulated cells might assist the cell to generate an AP. If so, such pixels should have been involved in grouped AP-evoking pixels during the mapping of AP induction, which were used for the prediction of neuronal position. Thus, the approximate position of the presynaptic cell could be determined from the positions of the grouped Ca2+-evoking pixels, although the exact cell cannot be identified.
We found that the distribution of innervating neurons in the local neocortical circuits appears to depend upon the lateral distance of the dendrite from the soma. This finding does not contradict the results of anatomical studies in which overlapping axonal and dendritic arbors were reconstructed [16, 17, 27–30]. Axons and dendrites tend to extend isotropically from the soma, and the density of their arbors decreases laterally over a few hundred microns. Thus, if presynaptic neurons are located on one side of the postsynaptic cell, the presynaptic axons would overlap with dendrites on the same side of the postsynaptic cell more frequently than those on the other side. We also found that large spines (>0.2 μm3) tended to be innervated by cells on the ipsilateral side, while small spines (<0.2 μm3) tended to be innervated by cells on both sides. These findings suggest that each dendritic branch may have a different receptive field in which the innervating neurons are located, and that this receptive field may be mediated primarily by large spines. However, it should be noted that synapses with a very low release probability or very low expression of NMDAR may be underestimated under the conditions used in this study.
It can be assumed theoretically that a functionally-associated group might innervate a specific dendritic branch of the postsynaptic cell to generate a nonlinear summation of synaptic inputs in the local dendrite [31–33]. In some invertebrates and vertebrates, distinct sensory inputs induce Ca2+ signals in specific dendrites in the visual and auditory systems [13, 34]. In the mammalian neocortex, functionally-associated cells are assumed to connect with each other with a higher probability, forming microcircuits [35–37]. However, these cells are not necessarily neighbours and, in this study, no clear clustering of presynaptic cells innervating the same dendritic branch was observed. Candidates for functionally connected and associated groups include subsets of neurons derived from the same stem cell  and subsets of the neurons innervating the same brain area [19, 39]. These subsets of neurons can be visualized specifically, and 2pMAPG can be used to stimulate visually-identified neurons at the level of a single cell . Thus, the detection method described here will allow clarification of whether or not such groups of neurons innervate the same dendritic branch, what part of dendrites they innervate, and what size of spines they innervate.
Two limitations to the present method need to be overcome in the future. First, the present rate of Ca2+ imaging is not fast enough to observe more than ~100 spines at once. In this study, the maximum number of spines that could be imaged simultaneously was 40, which represents only a few percent of the total number of spines on a single pyramidal cell. In order to observe more than a hundred scattered dendritic spines, 3D arbitrary movement of the scanning points will be useful . Second, this study was performed using slice preparations and, inevitably, axon fibres crossing the cutting plane were severed. The depth of the mapping area was also limited by slice thickness. Thus, it was difficult to clarify the distribution of all the presynaptic neurons innervating all the spines in the imaging region. Ideally, the mapping and imaging should be performed in vivo. In vivo Ca2+ imaging of dendritic spines has been reported, whereas in vivo two-photon uncaging of glutamate has not. However, 2pMAPG will be more applicable to in vivo studies than ultraviolet photostimulation, since the infrared (720-nm) light required for 2pMAPG can penetrate deeper into brain tissue than ultraviolet light with one-photon excitation. It has been reported recently that a newly-developed caged glutamate, RuBi-glutamate, can be activated by two-photon excitation at the longer wavelength of 800 nm . Alternatively, two-photon stimulation of Channelrhodopsin-2 (ChR2), a light-gated cation channel, might be more applicable to in vivo stimulation, since ChR2 excitation does not require the perfusion of any exogenous agent within the brain. In addition, the longer wavelength used for ChR2 excitation (920 nm) will stimulate a deeper cortical area than can be achieved with either CDNI- or RuBi-glutamate. As a large excitation volume is essential for two-photon excitation of ChR2 (MM unpublished data) , two-photon macro stimulation will be effective. Development of novel caged compounds and ChR2 variants will improve the performance of two-photon stimulation of neurons in vivo. In the future, specific clusters or specific distributions of presynaptic cells that could not be detected in this study may be revealed by combining photostimulation and fast Ca2+ imaging of more than 100 spines in vivo.
This study developed a novel method for simultaneously performing Ca2+ imaging in a narrow region that includes a segment of a dendrite and 2pMAPG across a broad area that includes many pyramidal cells. This technique allowed identification of various sizes of innervated spine located <140 μm laterally from the postsynaptic soma. Spines distal to their parent soma were preferentially innervated by cells on the ipsilateral side. Large spines (>0.2 mm3) tended to be innervated by cells on the ipsilateral side, while small spines (<0.2 mm3) tended to be innervated by cells on both sides. However, no cluster of neurons innervating the same dendritic branch was detected. The method described here is a valuable first step toward elucidating the basic microarchitecture of connectivity between neurons and synapses, and the stimulation of presynaptic cells that may induce nonlinear dendritic integration in the postsynaptic cell.
Slices (350-μm thick) of motor cortex were prepared from 17- to 20-day-old Sprague-Dawley rats in accordance with the procedure described by Kawaguchi et al.,  using a cutting solution containing 120 mM choline chloride, 3 mM KCl, 8 mM MgCl2, 1.25 mM NaH2PO4, 26 mM NaHCO3 and 25 mM glucose. Slices were incubated at 32°C for 30 min and then stored in an incubation chamber at room temperature (22°-25°C) for at least 1 h. Each slice was transferred to a recording chamber at room temperature. The extracellular solution contained 125 mM NaCl, 2.5 mM KCl, 2-3 mM CaCl2, 1 mM MgCl2, 1.25 mM NaH2PO4, 26 mM NaHCO3, 20 mM glucose, 200 μM Trolox (Aldrich, WI, USA), and 1.5 mM CDNI-glutamate . The extracellular solution (2-4 mL) was oxygenated and recirculated continuously. All experiments were approved by the animal experimentation committee of the Faculty of Medicine, University of Tokyo.
Patch-clamp electrodes (open-tip resistance, 4-8 MΩ) were filled with a solution containing 135 mM cesium gluconate, 4 mM MgCl2, 10 mM disodium phosphocreatine, 4 mM Na-ATP, 0.4 mM Na-GTP, 10 mM HEPES-CsOH, 45 μM Alexa Fluor 594 and 0.75 mM Fluo-5F (pH 7.2, 293 mOsm). QX314 (5 mM) and D600 (0.5 mM) were also included to minimize the occurrence of dendritic spikes and Ca2+ influx via voltage-gated Ca2+ channels. In Ca2+ imaging of dendritic spines during 2pMAPG mapping, recordings were obtained from layer 5 pyramidal cells in the agranular area located 60 ± 13 μm [mean ± standard deviation (SD), n = 18] deep and 825 ± 65 (SD) from the pia. Series resistance was 17 ± 7 (SD) MΩ. The Ca2+ imaging regions were 47 ± 23 (SD) μm deep (n = 25). During Ca2+ imaging, the membrane potential was held at -30 mV to remove the Mg2+ block of NMDARs. The liquid junction potential was not corrected. In experiments to detect APs in layer 2/3 pyramidal neurons under the whole-cell current-clamp mode, the intracellular solution contained 138 mM potassium gluconate, 4 mM MgCl2, 10 mM disodium phosphocreatine, 50 μM Alexa Fluor 594, 4 mM Na-ATP, 0.3 mM Na-GTP and 10 mM HEPES-KOH (pH 7.2, 297 mOsm). The mean resting potential of the cells was -72 ± 3 (SD) mV (n = 8). Data were low-pass filtered at 2 kHz, sampled at 5-10 kHz, and recorded using FV1000-MPE software (Olympus, Tokyo, Japan).
Electrical stimulation was performed using a glass pipette filled with Alexa Fluor 594 dissolved in extracellular solution containing 2 mM Ca2+. Alexa Fluor 594 was used to visualize the position of the pipette and to keep it away from the dendrite. A current of 20-50 μA was applied for 0.1 ms per stimulation.
Two-photon excitation imaging and uncaging of glutamate
Experiments were performed using an upright microscope (BX61WI; Olympus) and an FV1000-MPE laser-scanning microscope system. Since Ca2+ imaging required high spatial resolution and 2pMAPG mapping should be performed over a broad area, a water-immersion objective with a high-numerical-aperture (NA) and low-magnification configuration (XLUMPlanFI/IR 25×, NA of 1.05) was used. Two mode-locked femtosecond-pulse Ti:sapphire lasers (MaiTai HP and MaiTai HP DeepSee; Spectra Physics, CA, USA) set at 720 and 830 nm were connected to the laser-scanning microscope via two independent scanheads (Figure 2). The laser emitted from the MaiTai HP was chirp compensated prior to entering the scanhead.
For 2pMAPG, the diameter of the 720-nm laser beam was adjusted to underfill the back aperture of the objective. This adjustment was achieved by using a motor-driven stage (SGSP20-85; Sigma-Koki, Tokyo, Japan) to change the distance between the two convex lenses in the optical pathway prior to entering the scanhead (Figure 2). As a result, the effective NA was small and the focal volume was large. In addition, the laser intensity was increased to release much more caged glutamate and, therefore, to activate many more glutamate receptors near the focal volume than could be achieved at the diffraction limit . This modification allowed effective induction of APs in cells near the focal volume.
In order to image dendritic spines at high resolution, the diameter of the 830-nm laser beam was adjusted to overfill the back aperture of the objective. The FWHM of the focal volume of the laser beam at 830 nm was estimated to be 0.41 ± 0.01 (SEM) μm laterally and 1.57 ± 0.02 (SEM) μm axially (n = 10). The illumination time of the lasers was regulated by acoustic optical modulators (Figure 2). Fluorescence emitted from the specimen was separated using a 560-nm dichroic mirror (FF560; Semrock, NY, USA) and one of two barrier filters (FF01-510/84 [Semrock] or HQ 620/60 [Chroma Technology, VT, USA]), followed by detection with photomultiplier tubes in the green (G) and red (R) fluorescence, respectively (Figure 2).
Images of neuronal structure were acquired by two-dimensional scanning with the 830-nm laser at different depths and these images were stacked perpendicular to the image plane. Pixel lengths for imaging whole neurons and dendritic spines were 0.96 μm and 0.08-0.16 μm, respectively. In all figures with fluorescent images of whole neurons, the top of the image is closest to the pial surface. The locations of recorded cells and laminar borders were identified under trans-illumination of the 830-nm laser scanning with a low-magnification objective (MPlan N 5x, NA of 0.1).
For 2pMAPG mapping, 128 pixels (16 × 8, spaced 31 μm apart) were scanned. Within each pixel, laser-mediated photolysis at 720 nm was performed consecutively at 3 × 3 points using lateral intervals of 6 μm with a pulse-train duration of 9 ms (1 ms at each point) . The mapping was performed at 3 different depths, each separated by 50 μm. Brain tissue scatters light, and the strength of scattering is described by the average length of the distance between scattering events (ls) . To maintain constant laser power for photolysis (P = 32-35 mW) within the mapped plane at depth z from the slice surface, the laser power was adjusted to P/e-z/ls before entering the tissue slice, with ls set to 80 μm. The focal plane was moved by regulating a piezo actuator (PI 721, Physik Instrumente, Karlsruhe, Germany) attached to the objective (Figure 2 and Additional File 1: Figure S1A). In contrast to our previous experiments of 2pMAPG mapping to detect EPSCs,  Ca2+ imaging required a long time interval between each 2pMAPG (470 ms versus 100 ms) because Ca2+ transient decay (>200 ms) was much slower than EPSC decay (~20 ms). In addition, photobleaching of the fluorescence depended on the duration of imaging. Thus, the space between neighbouring 2pMAPG pixels was increased from 19 μm to 31 μm laterally and from 25-30 μm to 50 μm axially and the total number of 2pMAPG mapping pixels was reduced from 3072-5120 to 384. In order to keep the number of AP-evoking pixels during this rough mapping similar to that in our prior report (~8), the focal volume for 2pMAPG was increased approximately three-fold from the previous experiments .
Spine size was estimated as described previously  FWHM was measured for the heads of large, sphere-like spines (criterial spines) and then fitted to the FHWM-diameter curve, followed by estimation of the diameter and volume of the head. . After that, the volumes of other spines were estimated based on total fluorescence intensity. Ca2+ transients that occurred in spines during the first or second imaging frame after stimulation and with amplitude larger than the mean of G/Rbase and 5 CV of G/Rbase were analyzed as described in the main text. FV1000-MPE software, IPLab (BD Biosciences, MD, USA) and our own software programs based on LabView (National Instruments, TX, USA) were used for image processing. Data are presented as means ± SEM, unless stated otherwise. Error bars on graphs correspond to the SEM. Mann-Whitney U test, Spearman's rank correlation, Student's paired t test, and one-way ANOVA were used for statistical comparisons. A P value of < 0.05 was used as the criterion for a significant statistical difference.
We thank C Miura and R Takizawa for technical assistance.
This work was supported by Scientific Research on Priority Areas-Elucidation of neural network function in the brain (No. 20021008 to MM) and for a Young Scientist (A: No. 19680020 to MM), and by Grants-in-Aids for a Specially Promoted Area (No. 2000009 to HK) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan; by a Mitsubishi foundation grant to MM; and by National Institute of Health Grants GM65473 (to GCRE-D and HK) and GM53395 (GCRE-D).
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