Original Research ARTICLE
Back-propagation of physiological action potential output in dendrites of slender-tufted L5A pyramidal neurons
- 1 Department of Cell Physiology, Max Planck Institute for Medical Research, Heidelberg, Germany
- 2 Department of Neurophysiology, Brain Research Institute, University of Zürich, Zurich, Switzerland
- 3 Institut National de la Santé et de la Recherche Médicale Unité 862, NeuroCentre Magendie, Circuit and dendritic mechanisms underlying cortical plasticity, Bordeaux, France
Pyramidal neurons of layer 5A are a major neocortical output type and clearly distinguished from layer 5B pyramidal neurons with respect to morphology, in vivo firing patterns, and connectivity; yet knowledge of their dendritic properties is scant. We used a combination of whole-cell recordings and Ca2+ imaging techniques in vitro to explore the specific dendritic signaling role of physiological action potential patterns recorded in vivo in layer 5A pyramidal neurons of the whisker-related ‘barrel cortex’. Our data provide evidence that the temporal structure of physiological action potential patterns is crucial for an effective invasion of the main apical dendrites up to the major branch point. Both the critical frequency enabling action potential trains to invade efficiently and the dendritic calcium profile changed during postnatal development. In contrast to the main apical dendrite, the more passive properties of the short basal and apical tuft dendrites prevented an efficient back-propagation. Various Ca2+ channel types contributed to the enhanced calcium signals during high-frequency firing activity, whereas A-type K+ and BKCa channels strongly suppressed it. Our data support models in which the interaction of synaptic input with action potential output is a function of the timing, rate and pattern of action potentials, and dendritic location.
In cortical pyramidal neurons, action potentials (APs) are initiated in the axon and back-propagate into their dendritic arbors both in vitro and in vivo (Stuart and Sakmann, 1994; Larkum and Zhu, 2002; Waters et al., 2003; Bereshpolova et al., 2007); APs back-propagate into the basal (Antic, 2003; Kampa and Stuart, 2006; Nevian et al., 2007), oblique (Antic, 2003; Frick et al., 2003), and apical main and tuft dendrites (Schiller et al., 1995; Williams and Stuart, 2000; Larkum and Zhu, 2002). Some of the suggested functional roles of these back-propagating APs (bAPs) are to serve as a feedback signal to the dendrites and to interact with synaptic signals to regulate dendritic plasticity and neuronal AP output (Frick and Johnston, 2005; Waters et al., 2005; Sjöström et al., 2008). Back-propagation is active in cortical pyramidal neurons, but the amplitude of the bAPs gradually decreases with distance from soma. This decline depends on numerous factors such as coincidence with incoming synaptic input (Larkum et al., 1999; Stuart and Hausser, 2001), intrinsic excitability (Bernard and Johnston, 2003; Frick et al., 2004), inhibition (Larkum, 1999), and morphology (Schaefer et al., 2003). Another important factor determining the reliability of back-propagation is the frequency of the AP output (Spruston et al., 1995; Stuart et al., 1997; Larkum, 1999; Williams and Stuart, 2000).
Layer 5A (L5A) pyramidal neurons are a major type of output neurons in neocortical circuits. These neurons differ from L5B pyramidal neurons in many ways, including the morphology of their dendritic arbors, their intra- and sub-cortical connectivity, and firing properties in response to physiological stimuli (Manns et al., 2004; Schubert et al., 2006; de Kock et al., 2007; Frick et al., 2007; Lefort et al., 2009; Petreanu et al., 2009). In the barrel cortex of rodents the firing of neocortical neurons is sparse with low mean frequencies (Brecht, 2002; Celikel et al., 2004; Crochet and Petersen, 2006; de Kock et al., 2007). L5A pyramidal neurons, for instance, respond to whisker stimulation with on average <1AP per stimulus in anesthetized animals, and increase their firing rate to ∼5 Hz during whisking episodes (de Kock and Sakmann, 2009); nevertheless, their firing patterns are highly irregular and consist of a wide distribution of inter-spike frequencies (<1 to >200 Hz) (Manns et al., 2004; de Kock et al., 2007). The timing, frequency and amplitude of bAPs have strong implications for synaptic and intrinsic plasticity, dendritic electrogenesis, and neuronal output (Frick and Johnston, 2005; Dan and Poo, 2006; Sjöström et al., 2008). This causal relationship between bAPs and information processing/storage led us to explore: (i) the role of AP timing during physiological activity patterns in dendritic signaling; (ii) the reliance of back-propagation efficacy on dendrite type and location; (iii) the postnatal development of this form of dendritic signaling; (iv) the regulation of AP back-propagation by active conductances. To address these questions, we used physiological AP patterns previously recorded in L5A pyramidal neurons in the barrel cortex of anesthetized rats (courtesy of de Kock; de Kock et al., 2007); these firing patterns were replayed in vitro in the same neuron type and brain area, while measuring Ca2+ signals along the main apical, apical tuft, and basal dendrites.
This work extends previous studies on the frequency dependence of back-propagation in cortical neurons and is, to our knowledge, the first study specifically exploring signal propagation in dendrites of L5A pyramidal neurons. Our data indicate that the changes in instantaneous firing frequency during physiological AP trains have a crucial role for dendritic voltage and biochemical signaling. These findings may have important implications for the induction of dendritic electrogenesis and plasticity.
Materials and Methods
Slice Preparation and Solutions
Wistar rats (14- to 29-days old) were anesthetized using isoflurane, decapitated, and coronal slices (350-μm thick) were prepared from the ‘barrel field’ of somatosensory cortex. Experimental procedures were approved by the Animal Research Committee of the Max Planck Society and according to the guidelines laid out in the EU directive on animal welfare. Brain slices were incubated for 20–30 min at 36°C and then stored at room temperature until used. The extracellular solution for cutting and incubation contained (in mM): 125 NaCl, 25 NaHCO3, 2.5 KCl, 1.25 NaH2PO4, 6 MgCl2, 1 CaCl2, 3 myo-inositol, 2 Na-pyruvate, 0.4 ascorbic acid, 25 glucose. For the experiments, brain slices were transferred to the recording chamber and superfused with an extracellular recording solution that contained 125-mM NaCl, 25-mM NaHCO3, 2.5-mM KCl, 1.25-mM NaH2PO4, 1-mM MgCl2, 2-mM CaCl2, 25-mM glucose, and was bubbled with 95% O2/5% CO2 (pH 7.4). Recordings were made at near-physiological temperature of 32–36°C. For the pharmacology experiments, the following drugs were bath-applied (final concentrations): Nimodipine (10 μM, Tocris), Ni2+ (100 μM, Sigma-Aldrich), Cd2+ (500 μM, Sigma-Aldrich), paxilline (1 μM, Tocris), Ba2+ (150 μM, Sigma-Aldrich). Paxilline and nimodipine were dissolved in DMSO at stock concentrations of 1 mM and 10 mM, respectively, resulting in a final DMSO concentration of 0.1%.
Cell Identification and Electrophysiology
The cell layer 5A at the border of whisker-related barrel field of the somatosensory cortex was visualized at low magnification (5×) under bright-field illumination, and layer 5A pyramidal neurons were visualized with infrared gradient contrast microscopy using a Leica upright microscope, fitted with a 40×/0.8 numerical aperture water-immersion objective. Recording pipettes (4–6 MΩ) were pulled from borosilicate glass and filled with (in mM): 135 K-gluconate, 10 HEPES, 10 Phosphocreatine-Na, 4 KCl, 4 ATP-Mg, 0.3 Na-GTP, pH 7.2 (adjusted with KOH). Biocytin (1.5–2.5 mg/ml, Sigma, Munich, Germany) was added to the recording solution for later identification and morphological reconstruction of the neurons. Signals were recorded using an Axon Instrument amplifier (Axoclamp-2B), low-pass filtered at 3 kHz and sampled at 10–50 kHz.
Stimulation protocols were designed following previous experiments in which trains of action potentials were recorded juxtasomally from L5A pyramidal neurons in the barrel cortex of anesthetized rats (P25–30) in response to primary whisker stimulation. These data were kindly provided by Dr. C. de Kock (Free University of Amsterdam de Kock et al., 2007). These 500 ms-long traces are comprised of spontaneous action potential output and evoked firing (200-ms long whisker stimulation between 145 and 345 ms (for details see de Kock et al., 2007). We tested 10 whisker stimulation episodes from a representative experiment (de Kock, personal communication) containing two to five APs with various ISIs. The absolute time of each action potential during these 500-ms sequences was taken and a replica trace consisting of 3 ms-long current pulses at the respective time points produced (natural firing pattern). For illustration purposes and to avoid unnecessary duplication, only sequences that substantially differ from each other are shown in the figures. In addition, sequences are arranged in an ascending order of complexity. These natural firing patterns were compared to those evoked by the same number of action potentials presented at the mean frequency (mean firing pattern). Trains of action potentials at these fixed frequencies were generated in the same manner using 3 ms-long current injections.
The method used for high-resolution, multi-photon imaging of Ca2+ fluorescence was as described previously (Koester et al., 1999). Briefly, we used femtosecond laser pulses at 870–890 nm from a Ti:Sa-Laser (Mira 900F; Coherent, Santa Clara, CA, USA) pumped by a solid-state laser (Verdi 8W; Coherent), coupled to a galvanometer scanning unit (TCSNT; Leica Microsystems, Mannheim, Germany) that was mounted on an upright microscope (Leica DMLF) equipped with a 40× objective (HCX APO W40x/0.8 NA). Fluorescence was acquired using external non-descanned detectors (photomultiplier tubes, R6357, Hamamatsu Photonics, Herrsching, Germany) behind the objective and the condenser, yielding a high signal collection efficacy. The Ca2+ signals were recorded in line-scan mode with a temporal resolution of 2.2 ms/line. Recordings of membrane voltage and fluorescence were analyzed offline using commercial software with custom-written algorithms (Igor Pro; WaveMetrics, Lake Oswego, OR, USA). Neurons were filled with a combination of the calcium-sensitive dye Oregon Green 488 BAPTA-I (200 μM) or Fluo 5F (200 μM) and the calcium-insensitive dye Alexa 594 (20–50 μM; both dyes from Invitrogen, Carlsbad, CA, USA) added to the intracellular recording solution to visualize the dendritic arbors and measure Ca2+ signals within. Dyes were allowed to fill the neurons for at least 15–20 min before Ca2+ signals were measured; measurements from the apical tuft region were not taken before at least 45 min after the soma was patched.
Ca2+ transients are reported as relative changes in OGB-1 fluorescence and were calculated as ΔF/F (t) = (F(t)−F0)/(F0−FB), where F0 is the baseline fluorescence, taken within 200 ms before the stimulation and FB is the background fluorescence, derived from a non-stained background region. Single exponential fits to the decay of the fluorescence transients were made to calculate the peak amplitude, denoted as transient amplitudes. Fluorescence traces are averages of three to five trials and group data are represented as means ± sem. Dendritic length constants L1/e of calcium profiles were derived by fitting exponential functions to the profiles, or by taking the value when the profile had dropped to 1/e. GraphPad software Instat 3 and Prism 4 (GraphPad Software, San Diego, CA, USA) was used for statistical analysis. Statistical significance was calculated using paired t-tests and non-parametric Mann–Whitney U tests.
Staining for Reconstruction
After recording, biocytin-filled neurons were processed using standard procedures. Slices were fixed at 4°C for at least 24 h in PBS containing 0.4% paraformaldehyde, then incubated in 0.1% Triton X-100 solution containing avidin-biotinylated horseradish peroxidase (ABC-Elite; Camon, Wiesbaden, Germany). Subsequently, 3,3-diaminobenzidine was used as reactive chromogen until axons and dendrites were clearly visible (after 2–4 min). To enhance staining contrast, slices were occasionally postfixed in 0.5% OsO4 for 30–40 min before mounting on slides and embedding using Moviol (Clariant, Sulzbach, Germany).
Physiological Versus Mean AP Patterns – Apical Dendrites
First, we investigated the role of AP timing within firing patterns in the back-propagation efficacy along apical dendrites. To do this we triggered 500 ms-long physiological firing patterns (de Kock et al., 2007) in L5A pyramidal neurons at P25 and compared them with the corresponding mean firing patterns (same number of APs at mean frequency). While frequencies of the mean firing patterns were always <20 Hz, physiological firing patterns contained instantaneous frequencies of >200 Hz. bAP-evoked Ca2+ signals were measured at the soma (apical trunk close to soma), 400–500 μm from soma, and in the initial part of the apical tuft (∼650 μm from soma, primary tuft dendrite). For reference, the main branch point (BP) and the tip of the tuft of the L5A apical dendrite at P25 were on average 636 ± 63 μm and 794 ± 88 μm from soma (pia: 845 ± 89 μm, mean ± SD, n = 10), respectively. The diameters of the dendrites were: 2.7 ± 0.6 μm for apical trunk close to soma, 1.3 ± 0.2 μm for apical dendrite ∼400 μm from soma, 1.2 ± 0.1 μm for apical dendrite just before major branch point, 0.9 ± 0.1 μm for primary tuft dendrite; n = 5).
The results from one representative experiment at P25 are illustrated in Figure 1. Five selected sequences of physiological firing patterns (out of 10 tested) and the corresponding mean firing patterns are shown in Figure 1B, and the resulting Ca2+ signals are depicted in Figure 1C. A typical finding from our experiments was that at the soma/proximal dendrite both physiological and mean firing patterns evoked strong Ca2+ signals – albeit with very different rise times. In sharp contrast, only three out of ten physiological sequences examined (1, 3, and 4; none of the mean firing patterns) evoked Ca2+ transients in the distal half of the apical dendrite (and to some extent even the tuft region beyond the BP). A common feature of these specific sequences (also sequence 6) is the occurrence of short bursts of two or three APs with short inter-spike intervals (ISIs < 20 ms, f > 50Hz). The other physiological and all mean firing patterns, in contrast, are comprised of AP sequences of low frequencies (ISIs ≥ 70 ms, f < 15 Hz). The results from nine similar experiments are summarized in Figure 1D. Here, and throughout the manuscript, sample size always refers to number of branches, which is equal to the number of cells. The amplitude of the Ca2+ signals at the soma/proximal dendrite was strongly dependent on both the number, and the ISIs of the AP trains. However, the ISIs became progressively more important for determining Ca2+ signal amplitude with distance from soma. At a distance of 400–500 μm from soma, only AP trains containing high frequency components were capable of eliciting measurable Ca2+ signals. In this region, the peak amplitudes of the Ca2+ signals for sequences containing high-frequency components (sequences 1, 3, 6 and 4 (See Figure 2)) dropped to ∼55% (0.554 ± 0.152 ΔF/F, normalized to soma, n = 9), but were significantly larger than those evoked by mean firing patterns (0.024 ± 0.008 ΔF/F; n = 9; p = 0.032). Thus, the length constant (L1/e) for these firing patterns was significantly larger than for the corresponding mean firing patterns (L1/e physiological 553 μm + 42/−33 μm; L1/e mean 352 μm + 15/−26 μm). The Ca2+ transients evoked by sequences 3 and 4 (two APs ≥ 100 Hz) were even able to invade the initial part of the apical tuft region beyond the BP (0.397 ± 0.043 ΔF/F normalized to soma). Within the tuft, however, Ca2+ signals dropped steeply for all firing patterns (see below). Interestingly, sequences 1 and 6 contained high-frequency components but failed to elicit Ca2+ signals in the apical tuft region, perhaps due to their ISI distribution (see Figure 4D).
Figure 1. Physiological firing patterns back-propagate more efficiently into the apical arbor than mean firing patterns. (A) Two-photon fluorescence image of a layer 5A pyramidal neuron showing the positions of the line-scan Ca2+ measurements. (B) Five (out of ten tested) different physiological firing patterns (black traces) and the corresponding mean firing patterns (gray traces) triggered in a L5A pyramidal neuron at P25. Frequencies within the AP trains are given above the traces. (C) Ca2+ transients were measured at the soma, 450 μm from soma, and 650 μm from soma (tuft region) (schematic). Note that only AP sequence 3 back-propagated into the distal dendrite (arrows). Fluorescence changes are given as relative changes in the fluorescence of the Ca2+-indicator OGB-1 (ΔF/F) and are averages of 3–5 traces. (D) Peak amplitudes of Ca2+ transients (ΔF/F max, normalized) of physiological and mean firing sequences are plotted as function of distance from soma. Data were measured at the soma, at 400-500 μm and 600–700 μm from soma, and are given as mean ± sem (n = 9) normalized to the soma values. Dashed line indicates the strongest Ca2+ signal in the apical dendritic tuft (sequence 3) to emphasize the difference between the physiological and the mean firing pattern.
Figure 2. Physiological and mean firing patterns decline with a similar length constant along the basal dendrites. (A) Physiological firing patterns (black; sequences 1, 3, 4, and 6) and the corresponding mean firing patterns (gray) were triggered in a L5A pyramidal neuron at P25. (B) Ca2+ transients were measured at the soma, 75 μm, and 135 μm from soma across a basal dendrite. (C) Peak amplitudes of Ca2+ transients (ΔF/F max, normalized) are plotted as function of distance from soma. Data are given as mean ± sem (n = 6).
Physiological Versus Mean AP Patterns – Basal Dendrites
In L5A pyramidal neurons, basal dendrites comprise approximately 50% of the total dendritic length (Frick et al., 2008). We therefore examined how well physiological AP output back-propagates into the basal dendrites (Figure 2). Figures 2A,B shows the findings from an individual experiment. Ca2+ transients in response to physiological firing patterns (sequences 1, 3, 4, and 6) and the corresponding mean firing patterns were recorded at the soma (basal dendrite close to soma, diameter 1.4 ± 0.2 μm, n = 5), at 75 μm from soma, and at a distal location of 135 μm from soma (diameter at ∼120 μm from soma 0.7 ± 0.1 μm, n = 5; mean length for basal dendrites 162 ± 22 μm, mean ± SD, n = 12, P25). Similarly to the apical dendrites, the amplitude of the Ca2+ signals at the proximal basal dendrite was a function of both bAP number and ISIs. In contrast, the short ISIs of the physiological firing patterns did not substantially promote effective back-propagation into the distal half of the dendrite, resulting in comparable L1/e (L1/e physiological 96 + 13/−21 μm, L1/e mean 92 + 14/−11 μm, average of all seven firing sequences, average of all sequences containing at least two APs, n = 6). These experiments demonstrate that the properties of the basal dendrites are very different from those of the apical dendrites.
Critical AP Frequency for Apical Dendrites
In vivo, L5A pyramidal neurons of the barrel cortex rarely fire more than two or three APs at higher frequencies – either spontaneously or in response to whisker stimulation (Manns et al., 2004; de Kock et al., 2007). To further examine the critical frequency for efficient back-propagation within this activity range we therefore induced trains of three APs at fixed frequencies ranging from 20 to 140 Hz (Figure 3). The results from one experiment are illustrated in Figure 3B, upper panel, in which Ca2+ signals were measured in the apical dendrite ∼530 μm from soma. The amplitude of the Ca2+ signal was small at a frequency of 20 Hz (0.12 ΔF/F), but strongly increased with higher frequencies, reaching a maximum at 100 Hz (0.85 ΔF/F). Surprisingly, frequencies above this critical frequency (CF) evoked smaller transients (not shown). The results from 6 similar experiments are summarized in Figure 3B, lower panel. The CF varied from cell to cell, and was on average 91 ± 14 Hz (range 75–140 Hz, n = 6). The reliance on frequency was strongest in the dendritic region 300–400 μm from soma, were the Ca2+ transients increased substantially when frequencies approached the optimal frequency. In this dendritic region, Ca2+ transients evoked by AP trains at CF were on average ∼7- to 8-fold larger than those evoked by single APs (normalized to somatic values, 1.32 ± 0.17 ΔF/F, n = 6, versus 0.18 ± 0.15 ΔF/F, n = 6; p = 0.0041). In summary, higher frequencies (>40 Hz) were necessary to enable efficient AP back-propagation into the distal half of the apical dendrite.
Figure 3. Critical frequency for back-propagation of short AP trains in apical but not basal dendrites. (A) Reconstruction of a L5A pyramidal neuron at P25. Ca2+ measurements were taken at the soma and at three different distances along either the apical dendrite or the basal dendrite (indicated by the symbols and ranges). (B) Apical dendrites, upper panel. Ca2+ transients (ΔF/F) evoked by trains of three APs at different fixed frequencies measured at the main apical dendrite 532 μm from soma (see dashed line in A) in a P25 L5A pyramidal neuron. Lower panel. Normalized amplitudes of Ca2+ transients evoked by single APs (dashed line) and trains of APs at different frequencies are plotted as function of distance from soma. Average values are mean ± sem (n = 6). (C) Basal dendrites, upper panel. Ca2+ transients (ΔF/F) evoked by trains of three APs at different fixed frequencies measured in the basal dendrite 51 μm from soma in a P25 L5A pyramidal neuron. Lower panel. Peak ΔF/F Ca2+ signals evoked by single APs and AP trains at different frequencies are normalized and plotted against distance from soma (mean ± sem, n = 6). Comparison between apical and basal dendrites. (D) Peak Ca2+ signals elicited by single APs and trains of three APs at 100 Hz were normalized and plotted as function of distance for apical and basal dendrites. Distances were normalized with respect to the total length of these dendrites. (E) Ca2+ transients (ΔF/F max) evoked by three APs are plotted as function of frequency at 70% of the total basal and apical dendritic length. All data are from P25 neurons.
Lack of Critical AP Frequency for Basal Dendrites
The lack of amplification observed in basal dendrites using physiological AP patterns prompted the question of whether these dendrites possess a critical frequency within the physiological activity range of these neurons. Figure 3C, upper panel, shows the Ca2+ transients elicited in a basal dendrite ∼51 μm from the soma in response to bursts of three bAPs at varying frequencies. In this example (and confirmed in 6 experiments), the Ca2+ signals did not increase as a function of frequency (20–140 Hz; Figure 3C, lower panel). In 3 cells, frequences of up to 225 Hz were tested confirming the lack of amplification. Thus, Ca2+ transients of both single bAPs and bAP trains decayed with a similar L1/e of ∼90–100 μm, indicating that there might not be a CF, at least for short bAP trains, in basal dendrites.
Comparison of Apical and Basal Dendrites
Our analysis suggests that the dendritic properties determining back-propagation are strikingly different for apical and basal dendrites. Since the length of these dendrite types differs by ∼5-fold (apical ∼800 μm versus basal dendrites ∼160 μm), we compared back-propagation properties as a function of fractional length (Figures 3D,E). Figure 3D shows the normalized Ca2+ amplitudes evoked by single APs and trains of three APs at 100-Hz along the apical and basal dendrites for six L5A pyramidal neurons. Single bAPs evoked Ca2+ signals that attenuated more strongly along the first 60–70% of the apical dendrite (L1/e apical 272 + 26/−19 μm, 0.36 fractional length, n = 6) as compared to basal dendrite (L1/e basal 92 + 30/−15 μm; 0.55 fractional length; n = 6), but failed to produce Ca2+ signals in the distal 30% of either dendrite type. Ca2+ signals evoked by AP trains at 100 Hz were significantly increased in the apical dendrites, but not in the basal dendrites (Figures 3D,E; apical dendrite, signal decay to 1/e of somatic values 596 ± 53 μm, ∼0.85 fractional length; basal dendrite, L1/e 93 + 25/−18 μm, 0.56 fractional length; n = 6). This analysis strengthens the conclusion that the active properties of basal and apical dendrites are very different.
The Apical Tuft Region as a Separate Dendritic Zone
Our previous results indicate that firing patterns containing high-frequency components (e.g. physiological sequences 3 and 4) can reach the apical tuft, but that the Ca2+ signals drop off steeply within the tuft. We set out to investigate back-propagation into the tuft in more detail (Figure 4). Figure 4A shows the tuft region and measurements of the Ca2+ signals produced by three bAPs at 100 Hz just before the BP (position 1), and at two dendritic sites within the tuft. The Ca2+ signal evoked in the dendrites just before the BP had almost vanished ∼20 μm into the tuft region. This strong attenuation resulted in a small L1/e (∼30 μm starting from position 1, Figure 4B, n = 5) that was ∼3-fold and ∼20-fold smaller when compared to the basal dendrite (L1/e < 100 μm) and the main apical dendrite (L1/e ∼600 μm), respectively. Next, we addressed the question of whether the Ca2+ transients in the tuft depend on the number of bAPs or the AP timing within the bursts. Figure 4C demonstrates that increasing the number of APs within the high-frequency train enhanced the Ca2+ influx within the apical tuft. To probe the reliance of the Ca2+ signals on the AP timing, a regular 3 AP-sequence at 100 Hz was compared with those, were the 2nd AP was shifted ±5 ms (Figure 4D). Sequences containing equal ISIs or a shorter ISI (5 ms) followed by the longer one (15 ms) resulted in a comparable Ca2+ influx, whereas the reverse order produced a reduced Ca2+ signal. These data suggest that both the number of APs and the distribution of ISIs within a firing pattern are important factors for the regulation of back-propagation efficacy.
Figure 4. Ca2+ signals steeply drop within the apical dendritic tuft. (A) Photograph of the apical tuft region of a L5A pyramidal neuron indicating the positions for Ca2+ imaging with respect to the major BP. Ca2+ signals were produced by a train of three APs at 100 Hz and strongly attenuated beyond the BP (position 2). (B) ΔF/F Ca2+ signals plotted as a function of distance from a position close to the BP (n = 5). (C) ΔF/F Ca2+ signals were evoked by short trains of 2–4 APs at 100 Hz and measured at three distances before the BP and within the tuft. (D) Dendritic Ca2+ signals depend on changes in instantaneous ISIs. Trains of three APs at 100 Hz (regular train) were compared with those in which the 2nd AP was shifted ±5 ms in a region ∼500 μm from soma before the BP (n = 5). ΔF/F Ca2+ signals were normalized to the regular AP train. Data for this figure were from P14 (A–C) and P25 (D) neurons.
Maturation of Back-Propagation during Postnatal Development
Does the back-propagation efficacy in L5A dendrites change during the postnatal period between P14 and P25? To address this question, physiological and mean firing patterns were triggered in L5A pyramidal neurons at P14 and the evoked Ca2+ transients were measured along the apical and basal dendrites (Figures 5, 6 and 7C). Similar to P25 dendrites, firing patterns containing high-frequency components substantially improved back-propagation efficacy into the distal half of apical dendrites (Figures 5 and 6), but not basal dendrites (Figure 6).
Figure 5. Backpropagation of physiological firing patterns into the apical dendrites at P14. (A) Five (out of ten tested) different natural firing patterns (black traces) and the corresponding mean firing patterns (gray traces) were evoked by somatic current injection in a layer 5A pyramidal neuron at P14. Frequencies within the AP trains are given above and the sequence numbers below the traces. (B) Ca2+ transients elicited by these AP sequences were measured at the soma, 450 μm from soma, and 650 μm from soma (tuft region) across the apical dendritic arbor (see schematic). Note that only AP sequences containing high-frequency components (arrows) back-propagate into the distal half of the apical dendritic arbor. Fluorescence changes are given as relative changes in the fluorescence of the Ca2+-indicator OGB-1 (ΔF/F) and are averages of 3–5 traces. (C) Peak amplitudes of Ca2+ transients (ΔF/FMax, normalized) of natural and mean firing sequences are plotted as function of distance from soma. Data were measured at the soma, at a region 400 to 500 μm from soma, and at a region 600 to 700 μm from soma, and are given as mean ± sem (n = 9) normalized to the soma values. Dashed line indicates the strongest Ca2+ signal that could be evoked in the apical dendritic tuft (sequence 1) to emphasize the difference between the natural and the mean firing pattern.
Figure 6. Comparison between apical and basal dendrites at P14. (A) Reconstruction of a L5A pyramidal neuron at P14. Trains of three APs were evoked by current injections into the soma and calcium measurements were taken at the soma and at three different distances along either the apical dendrite or the basal dendrite (indicated by the symbols and ranges). (B) Apical dendrites, upper panel. Ca2+ transients (ΔF/F) evoked by trains of three APs at different fixed frequencies measured at the main apical dendrite close to the major branch point (548 μm from soma, see arrow) in a P14 L5A pyramidal neuron. Frequencies ranged from 20 Hz to 100 Hz. Note that the maximal response was evoked at 50 Hz. Lower panel. Peak amplitudes of Ca2+ transients (n = 6) evoked by trains of three APs at different frequencies are normalized to the somatic values and plotted as function of distance from soma. For comparison, Ca2+ transients evoked by single APs (dashed line) are also shown. Average values are mean ± sem. Note that the frequency is becoming increasingly important at distances from soma more distal than 300 μm, and that signals drop off steeply beyond the major branch point within the apical tuft. (C) Basal dendrites, upper panel. Ca2+ transients (ΔF/F) evoked by trains of three APs at different fixed frequencies measured at the basal dendrite ∼50 μm from soma in a P14 L5A pyramidal neuron. Frequencies ranged from 20 to 100 Hz. Lower panel. Peak ΔF/F Ca2+ signals evoked by single APs and short trains of three APs at different fixed frequencies ranging from 20 to 140 Hz are normalized and plotted against distance from soma along the basal dendrites (n = 6). Note that there is no significant difference in the efficacy of back-propagation within this frequency range. (D,E) Comparison of apical versus basal dendrites. (D) Peak Ca2+ signals elicited by single APs and trains of three APs at 50 Hz were normalized and plotted as function of distance from soma. Distances along the basal and apical dendrites were normalized with respect to the total length of the dendrites to enable comparison of back-propagation efficacy across different dendrite compartments. Note the significant differences in back-propagation for apical and basal dendrites. (E) Differences in frequency-dependence are compared for a normalized distance of ∼70% along the basal (80–100 μm) and apical (400–500 μm) dendrites. Ca2+ signals evoked by trains of three APs at different frequencies were normalized to the 20-Hz train. Note the steep amplification in Ca2+ influx at the apical dendrite with increasing frequency.
Figure 7. Maturation of back-propagation during postnatal development. (A) Cumulative probability plot of the CFs for short trains of three APs for layer 5A pyramidal neurons at P14 and P25 (n = 6 for each age group). Dashed lines indicate the CF-ranges from 40–75 Hz at P14 and 75–125 Hz at P25 (corresponding to 1/6 and 5/6 of cumulative probability). (B) Normalized (to soma) peak ΔF/F Ca2+ signals evoked by single APs and bursts of three APs at the respective CF at P14 (60–75 Hz) and P25 (100–125 Hz) as function of normalized distance from soma (mean ± sem, n = 6 for each age group). (C) Normalized peak ΔF/F Ca2+ signals of physiological firing patterns (sequences 1, 3, 4, and 6) as function of distance from soma for P14 and P25 L5A pyramidal neurons (mean ± sem, n = 9 for each age group).
Figure 7 compares several aspects of back-propagation along the apical dendrite for the two age groups P14 and P25. The CF of AP bursts to induce significant amplification of the Ca2+ signals increased significantly from 55 ± 9 Hz (CFP14, range 40–75 Hz, n = 6, P14) to 91 ± 13 Hz (CFP25, range 75–140 Hz, n = 6; p = 0.036, P25) (Figure 7A). We also compared the Ca2+ profile for single APs, short AP trains, and for physiological AP patterns along the apical dendrite (Figures 7B,C). Single APs back-propagated more efficiently at P14 compared to P25, whereas the profile for trains of three APs at the respective CFs (CFP25 and CFP14) was more complex. For these AP trains, back-propagation was more efficient along the first half of the dendrite at P25 than at P14, while the reverse was true for the distal half of the dendrite (Figure 7B). Physiological firing patterns containing two APs at ∼CFP25 back-propagated more efficiently at P25 (Figure 7C). The Ca2+ profile for the physiological firing sequence 1 (three APs at high frequencies) matched the profile for trains of three APs at high frequencies, i.e. the Ca2+ signals produced in the distal dendrite were larger for P14 than P25.
Dendritic Electrogenesis Involves the Recruitment of Different Ca2+ and K+ Channels
Next, we probed the role of voltage-gated ion channels in the Ca2+ influx during AP back-propagation in the apical dendrites 300–400 μm from soma at P25. Specifically, we tested the involvement of Ca2+ channels (L-type, T-/R-type, all types), large-conductance Ca2+-dependent K+ channels (BKCa), and transient A-type K+ channels (Figure 8). Single bAPs, as well as bursts of three bAPs above (100 Hz) and below (20 Hz) CF were triggered while measuring the resulting Ca2+ transients. The application of 10-μM nimodipine to block L-type Ca2+ channels reduced the Ca2+ transient evoked by the 100-Hz bAP burst by ∼15% (0.85 ± 0.07, n = 5, p = 0.041; Figures 8A,B). Blockade of T-/R-type Ca2+ channels by application of 100-μM Ni2+ reduced the remaining transient by ∼20% (0.68 ± 0.12, n = 5, p = 0.044). Further addition of 500-μM Cd2+ completely blocked the Ca2+ transient (0.038 ± 0.025, n = 5, p = 0.007). The specific BKCa blocker paxilline (1 μM) significantly increased the Ca2+ transient associated with the 100-Hz AP burst (2.44 ± 0.45, median 2.51, n = 4, p = 0.011; Figures 8C,D). Similarly, blocking A-type K+ channels by low concentrations of Ba2+ (150 μM, specific for this channel at this concentration) increased the Ca2+ transient (1.46 ± 0.16, median 1.29, n = 5, p = 0.0185).
Figure 8. Dendritic electrogenesis is regulated by Ca2+ and K+ channels. (A) Effect of the following Ca2+ channel blockers on Ca2+ signals (ΔF/F) evoked by trains of three APs at 100 Hz at the apical dendrite 425 μm from soma in a P25 neuron: nimodepine (nim, 10 μM, L-type), Ni2+ (100 μM, T-/R-type), and Cd2+ (500 μM, all Ca2+ channels). All traces were normalized to the control trace. (B) Group data for the effect of Ca2+ channel blockers (normalized to control, mean ± sem, n = 5). (C) Effect of BKCa (1 μM paxilline) and A-type K+ (150 μM Ba2+) channel blockers on the Ca2+ signals produced by bursts of three APs at 100 Hz 300–400 μm from soma in the apical dendrite in P25 neurons. (D) Average data (mean ± sem) from nine similar experiments (nBa = 5, nPax = 4) normalized to control. All data are from P25 neurons.
Single bAPs and low-frequency (20 Hz) bursts of three bAPs produced little or no Ca2+ signal 300–400 μm from soma, preventing us from examining Ca2+ channel contribution. Thus, only the effects of blockers on BKCa channels and A-type K+ channels were quantified. In contrast to high-frequency bursts, 20-Hz bursts caused only a moderate activation of BKCa channels (1 μM paxilline, 1.34 ± 0.35, median 1.47, n = 4, p = 0.513). On the contrary, A-type K+ channels significantly suppressed Ca2+ transients evoked under those conditions (150 μM Ba2+, 3.85 ± 0.93, median 3.32, n = 6, p = 0.0134).
Our major conclusion is that the temporal composition of physiological firing patterns consisting of variable instantaneous frequencies determines back-propagation efficacy of the apical dendritic arbor. Specifically, we found that even two APs at CF significantly increase the amplitude of Ca2+ influx into the distal half (excluding the tuft region) of L5A apical dendrites. This CF shifted during early postnatal maturation from ∼55 Hz at P15 to ∼90 Hz at P25. In contrast, mean firing patterns with frequencies of <20 Hz back-propagated inefficiently into the distal apical dendrites. Furthermore, we show that the rules governing back-propagation are dendrite type-specific, in that there was no comparable amplification in back-propagation observed for the basal dendrites or the tuft region of the apical arbor. We also examined the role of various voltage-gated ion channels in regulating back-propagation during these different activity regimes. To our knowledge, this is the first study investigating the active properties of L5A pyramidal neuron dendrites, and our data further underline the importance of studying neuronal properties in a manner that reflects the activity of the specific cell type under investigation.
Validity of Studying Back-Propagation in Vitro
Neocortical brain slices exhibit a lower synaptic background activity than that occurring in vivo. In spite of this, several studies demonstrate that the amplitude of bAPs in L2/3 and L5B pyramidal neurons is similar in vivo and in vitro (Helmchen et al., 1999; Larkum and Zhu, 2002; Waters et al., 2003; Bereshpolova et al., 2007; Bar-Yehuda and Korngreen, 2008). Together, this work supports the idea that bAPs are a robust and reliable property of pyramidal neurons during different states of network activity.
Effective Back-Propagation into the Apical Dendrites during Physiological AP Patterns
We show that, in L5A pyramidal neurons, low-frequency (≤20 Hz) AP firing fails to efficiently invade the distal half of the apical dendritic arbor. In contrast, efficient back-propagation is evoked by physiological or regular AP patterns containing higher frequencies, particularly at the CF (Figures 1, 3 and 5–7). Since bAPs are important in a variety of neuronal processes (including STDP; Magee and Johnston, 1997; Markram et al., 1997; Dan and Poo, 2006), the induction of intrinsic plasticity; Frick et al., 2004 and local synaptic integration; Larkum et al., 1999; Stuart and Hausser, 2001), efficient back-propagation during physiological firing patterns will also determine the rules for information processing and storage (Frick and Johnston, 2005; Dan and Poo, 2006; Sjöström et al., 2008).
Comparison between Apical, Basal, and Tuft Dendrites
In contrast to the main apical dendrites, neither physiological firing patterns nor short high frequency bursts of APs are able to enhance back-propagation into the 5A basal dendrites. As a result, the degree of attenuation (L1/e) for high-frequency AP bursts is approximately 6-fold higher for basal compared to apical dendrites (Figure 3D). In the apical tuft, in contrast to the main apical and basal dendrites, no Ca2+ influx is produced by low frequency firing (Figures 1, 3 and 5). Even physiological AP patterns/regular AP trains containing CF components produce only small Ca2+ transients that drop steeply beyond the BP (L1/e ∼30 μm for three APs at 100 Hz, Figure 4). Differences in back-propagation properties between main apical, apical tuft, and basal dendrites may reflect differences in the expression levels and/or types of voltage-dependent conductances, and in the dendritic morphology.
Comparison with L2/3 and L5B Pyramidal Neurons
Back-propagation in apical dendrites
Our data suggest that for low-frequency (≤20 Hz) firing, back-propagation in L5A pyramidal neurons is more efficient than in L2/3 pyramidal neurons but weaker compared with L5B pyramidal neurons (Schiller et al., 1995; Larkum, 1999; Waters et al., 2003; Larkum et al., 2007). An amplification in the Ca2+ signals by high-frequency bAP firing has been previously described for both L2/3 and L5B pyramidal neurons (Larkum, 1999; Williams and Stuart, 2000; Waters et al., 2003). The CF for efficient back-propagation reported here for L5A pyramidal neurons (∼90 Hz) is either slightly smaller (L2/3, ∼130 Hz; Larkum et al., 2007) or similar (L5B, ∼100 Hz; Larkum, 1999) compared with these neurons.
Back-propagation in basal dendrites
In contrast to L5A, Ca2+ transients evoked by single bAPs do not attenuate along the basal dendrites of L5B pyramidal neurons (Kampa and Stuart, 2006; Nevian et al., 2007), and regenerative Ca2+ influx may or may not be recruited by high-frequent AP activity in these neurons (Kampa and Stuart, 2006; Nevian et al., 2007). In L5A pyramidal neurons, we did not observe a significant increase in the Ca2+ transients of basal dendrites within the physiological activity range (Manns et al., 2004; Frick et al., 2007; de Kock and Sakmann, 2009) for these neurons.
Back-propagation into the distal tuft
Similar to the results obtained for L2/3 neurons (Waters et al., 2003), but in contrast to those from L5B (Schiller et al., 1995; Larkum, 1999), single APs and short low-frequency AP patterns failed to produce Ca2+ signals in the tuft beyond the major BP. High-frequency AP patterns, on the other hand, evoked small Ca2+ signals within the tuft (similar to L2/3 pyramidal neurons for comparable AP numbers) (Waters et al., 2003). These signals, however, were strongly attenuated along the primary tuft dendrites with L1/e of ∼30 μm from major BP (three APs at 100 Hz). This attenuation was much more pronounced than that observed in the primary tuft dendrites of L5B pyramidal neurons (Larkum, 1999), and more similar to that recorded in the higher-order tuft branches in these neurons (Helmchen et al., 1999; Larkum and Zhu, 2002). One explanation for these findings is that the primary tuft dendrites of L5A pyramidal neurons contain a lower density of active conductances, resulting in a more passive membrane and an increase in the threshold for dendritic electrogenesis. It is possible that Ca2+ spikes in the tuft dendrites can be evoked by the coincidence of bAPs and synaptic input, thereby increasing the gain of these neurons.
AP Firing Patterns and Dendritic Electrogenesis
The variability in AP timing of physiological activity patterns could convey important information, reflecting the precise integration of spatio-temporal patterns of synaptic inputs; alternatively, this irregularity may reflect noise and information could be represented by mean firing rates recorded over hundreds of milliseconds (Mainen et al., 1995; Shadlen and Newsome, 1995; Nowak et al., 1997; Stevens and Zador, 1998; Ahissar et al., 2000; Panzeri et al., 2001). Our study shows that the efficacy of AP back-propagation along L5A apical dendrites strongly correlates with the distribution of instantaneous ISIs during physiological activity patterns. These data lend support to the idea that the temporal structure of physiological firing patterns may contain important information for dendritic signaling and plasticity (Williams and Stuart, 2000). Short bursts of action potentials in physiological spike trains have been suggested to transmit significant informational content (reviewed in Lisman, 1997).
Ion Channels Regulating AP Back-Propagation
It was hitherto unknown which active conductances shape AP back-propagation in L5A pyramidal neurons. In L5B pyramidal neurons, low-voltage (T-type) and high-voltage (L- and N-type) Ca2+ channels, A-type K+ channels, and BKCa channels are present in the apical dendrites (Migliore and Shepherd, 2002; Benhassine and Berger, 2005). We found that low- and high-voltage Ca2+ channels (T-/R-, L-, and others) are activated in the apical dendrites of L5A neurons during regimes of high frequency AP activity. Our results also demonstrate that A-type K+ channels strongly dampen dendritic excitability, both during low- and high-frequent AP activity, in agreement with findings from hippocampal CA1 pyramidal neurons (e.g. Hoffman et al., 1997; Frick et al., 2003). BKCa channels and A-type K+ channels significantly dampened the high-frequency bAP burst-evoked Ca2+ signals. In contrast to A-type K+ channels, however, BKCa channels were not significantly activated by single bAPs or low-frequency bAP bursts. This is consistent with a recent study showing that BKCa channels increase the threshold for dendritic electrogenesis (Benhassine and Berger, 2009), but that their activation requires a large Ca2+ influx (Benhassine and Berger, 2005). Our results are a first step in determining the source of Ca2+ signals, and the ion channels that dampen dendritic excitability in the dendrites of L5A pyramidal neurons.
Developmental Change in AP Back-Propagation
Our results show that the profile of AP-associated Ca2+ signals along the apical dendrites changes during postnatal development. For the apical dendrites, the attenuation of Ca2+ signals evoked by single APs and low-frequency (≤20 Hz) AP trains increased with age. Physiological AP patterns containing high-frequency components (mostly two APs, e.g. sequences 3,4, and 6), however, propagated more efficiently towards the distal dendrite at P25 compared with P14. Ca2+ signals evoked by trains of three APs at fixed frequencies suggest that at P25 the largest amplification occurs in more proximal dendritic regions (∼300 μm) when compared with P14 (∼500 μm). In contrast to most physiological AP patterns, but similar to sequence 1 (three APs at high frequencies), these signals attenuated more strongly within the distal half of the dendrite than at P14. This suggests that at P14 an additional AP has a larger amplifying effect on back-propagation than at P25. We also observed an increase in the CF from ∼55 to ∼90 Hz between P14 and P25 days of postnatal development. For the basal dendrites, AP-Ca2+ signal attenuation was more pronounced at P14 than at P25, and no amplification was observed for the activity patterns tested at both ages. The most plausible explanation for these changes in dendritic excitability during development is a change in the expression levels of active conductances in the dendrites (Hamill et al., 1991; Zhu, 2000; Atkinson and Williams, 2009).
In summary, we conclude that the active dendritic properties of L5A pyramidal neurons strongly depend on the age and the type of dendrite – setting up largely different rules for information processing and plasticity in the main apical, apical tuft, and basal dendrites, respectively. Accordingly, these different dendritic arbors will have branch specific rules for the propagation of physiologically occurring action potential output and for its coupling with synaptic input. In this way, these different rules could improve the storage and processing capabilities of L5A pyramidal neurons. Lastly, our study supports the idea that the different role L5A and L5B pyramidal neurons play within the neocortical circuitry is established by their distinct morphological, connectivity, and now dendritic criteria.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The authors wish to thank Drs. F. Helmchen, B. Kampa, and M. Ginger for valuable comments on the manuscript, Mrs. M. Kaiser and E. Stier for technical assistance, and Dr. C. de Kock for providing the in vivo L5A activity data. Part of this work was performed at the Cellular Imaging Facility (PICIN) at the Neuroscience Institute, Bordeaux. Research supported by the Max Planck Society, an AVENIR grant of the Institut National de la Santé et de la Recherche Médicale (INSERM), and the Network of European Neuroscience Institutes (ENI-Net).
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Keywords: layer 5A, critical frequency, temporal code, development, voltage-gated ion channels, dendritic excitability
Citation: Grewe BF, Bonnan A and Frick A (2010) Back-propagation of physiological action potential output in dendrites of slender-tufted L5A pyramidal neurons. Front. Cell. Neurosci. 4:13. doi: 10.3389/fncel.2010.00013
Received: 24 November 2009;
Paper pending published: 20 December 2009;
Accepted: 16 April 2010; Published online: 18 May 2010
Edited by:Daniel Johnston, University of Texas, USA
Reviewed by:Nelson Spruston, Northwestern University, USA
Jeff Magee, Howard Hugues Medical Institute, USA
Copyright: © 2010 Grewe, Bonnan and Frick. This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
*Correspondence: Andreas Frick, Institut National de la Santé et de la Recherche Médicale Unité 862, NeuroCentre Magendie, Circuit and dendritic mechanisms underlying cortical plasticity, Université Bordeaux 2, ENI-NET 146, rue Léo Saignat 33077 Bordeaux, France. e-mail: firstname.lastname@example.org