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Parvalbumin-expressing fast-spiking (FS) cells are interconnected via GABAergic and electrical synapses and represent a major class of inhibitory interneurons in the neocortex. Synaptic connections among FS cells are critical for regulating network oscillations in the mature neocortex. However, it is unclear whether synaptic connections among FS interneurons also play a central role in the generation of patterned neuronal activity in the immature brain, which is thought to underlie the formation of neocortical circuits. Here, we investigated the developmental time course of synaptogenesis of FS cell in mouse visual cortex. In layer 5/6 (L5/6), we recorded from two or three FS and/or pyramidal neurons (P) to study the development of electrical and chemical synaptic interactions from postnatal day 3 (P3) to P18. We detected no evidence for functional connectivity for FS-FS or FS-P pairs at P3–4. However, by P5–6, we found 20% of FS pairs were electrically coupled and 24% of pairs were connected via GABAergic synapses and by P15–18, 42% of FS pairs had established functional electrical synapses and 47% of FS pairs were connected via GABAergic synapses. FS cell GABAergic inhibition of pyramidal cells showed a similar developmental time line, but no electrical coupling was detected for FS-P pairs. We found that synaptogenesis of electrical and GABAergic connection of FS cells takes place in the same period. Together, our results suggest that chemical and electrical connections among FS cells can contribute to patterned neocortical activity only by the end of the first postnatal week.
Parvalbumin-containing fast-spiking neurons (FS cells) are the most prominent GABAergic neurons in the neocortex (Kawaguchi and Kubota, 1997; Uematsu et al., 2008). In rodents, the birthdate of FS cells peaks at embryonic day 17 (E17) (Hevner et al., 2004; Butt et al., 2005; Rymar and Sadikot, 2007). At postnatal day 1 (P1), inhibitory neurons are already present in the infragranular layers of the neocortex (Rymar and Sadikot, 2007).
In the newborn animal, these FS cells could, in principle, already be connected via electrical and/or GABAergic synapses, allowing them to form functional networks at birth. However, when during development FS cells form GABAergic and electrical connections has not yet been determined.
The functional connectivity of GABAergic neurons is of special interest as they have been implicated in generating patterned neuronal activity in both juvenile and adult neocortex (Jefferys et al., 1996; Ben-Ari, 2001; Klausberger et al., 2003; Ben-Ari et al., 2004; Hestrin and Galarreta, 2005; Cardin et al., 2009; Sohal et al., 2009). The coordinated activity of neocortical neurons in newborn animals is thought to be important for the normal development of neocortical circuits (Katz and Shatz, 1996; Ben-Ari, 2001; Ben-Ari et al., 2004; Adelsberger et al., 2005; Cang et al., 2005; Moody and Bosma, 2005; Hanganu et al., 2006). The connectivity and synaptic properties of connections among GABAergic cells are thought to determine the intensity and frequency of their oscillatory activity (Jefferys et al., 1996; Bartos et al., 2002; Bartos et al., 2007). There is evidence that both electrical and chemical synapses are involved in the generation of patterned activity in the immature neocortex (Peinado, 2001; Dupont et al., 2006). Previous reports have suggested that electrical synapses are extensive in the immature brain and that, during maturation, the prevalence of electrical synapses diminishes while the prevalence of chemical synapses increases (Peinado et al., 1993a; Peinado, 2001; Montoro and Yuste, 2004; Sutor and Hagerty, 2005). These data suggest that the initial local circuits in the neocortex are based on electrical coupling and that only later in the maturation process chemical synapses become dominant (Montoro and Yuste, 2004). Furthermore, studies using paired recordings determined that electrical coupling is present among thalamic relay neurons and among inhibitory neurons in the thalamic reticular nucleus in newborn mice (Parker et al., 2009; Lee et al., 2010). However, whether electrical connections among FS cells are present in the postnatal neocortex and whether gap junctions form prior to GABAergic synapses in the newborn cortex has not been determined directly.
In this study we used transgenic mice that selectively express enhanced green fluorescent protein (EGFP), in parvalbumin-positive FS cells (Chattopadhyaya et al., 2004). We recorded from two or three EGFP-expressing cells simultaneously in patch-clamp configuration and determined the cells’ electrophysiological responses, synaptic connectivity and synaptic properties. This approach allowed us to characterize the developmental time course of GABAergic and electrical connections among FS cells and between FS cells and pyramidal neurons in the early postnatal period.
FS cells were identified in a mouse strain (G42) expressing enhanced green fluorescent protein (EGFP) under the control of the glutamic acid decarboxylase 67 (GAD67) promoter (Chattopadhyaya et al., 2004). Postnatal day 3 (P3) to P18 mice of both sexes were anesthetized by inhalation of isofluorane. Brains were removed and immersed in ice-cold solution containing (in mM): 87 NaCl, 2.5 KCl, 1.25 NaH2PO4, 7 MgSO4, 0.5 CaCl2, 25 NaHCO3, 25 glucose, 75 Sucrose (pH 7.4, 315 mOsm). Parasagittal cortical slices (300 μm, 30° angle) were obtained by using standard procedures (Galarreta et al., 2008). Initially, slices were incubated at 32–34°C for 25 min in the same solution. Subsequently, the slices were maintained for at least 25 minutes at room temperature in an oxygenated solution containing (in mM): 125 NaCl, 2.5 KCl, 1.25 NaH2PO4, 1 MgSO4, 2 CaCl2, 26 NaHCO3, 20 glucose, 4 lactic acid, 2 pyruvic acid, 0.4 ascorbic acid (pH 7.4, 315 mOsm; aCSF). Individual slices were transferred from the holding chamber to a submersion-type recording chamber, perfused with oxygenated aCSF at a rate of 2–4 mL/min and maintained at 32–34°C. Recordings were obtained from L5/6 of the visual cortex. Fluorescent cells were visually identified using an upright microscope (Axioskop, Zeiss, Thornwood, NY) illuminated with a Xenon lamp (150 W, Opti-Quip, Highland Mills, NY) and equipped with a 40x water immersion objective lens (Zeiss, NA: 0.8) and EGFP filters (XF100, Omega Optical, Brattleboro, VT). Selected fluorescent interneurons, as well as pyramidal cells, were visualized using infrared differential interference contrast video microscopy (C2400, Hamamatsu, Bridgewater, NJ) and recorded using conventional patch-clamp techniques. All putative FS neurons were identified by their firing behavior in current clamp as EGFP-positive FS cells showed characteristic discharges of high-frequency, non-adapting spike trains in response to near-threshold current injection (Kawaguchi, 1997).
To test for connectivity via GABAergic and electrical synapses, simultaneous recordings were obtained from two or three FS and/or pyramidal cells using Axopatch 200B amplifiers (Axon Instruments, Union City, CA). In total, we tested 278 possible connections among FS cells (FS → FS) and 78 possible connections between FS cells and pyramidal neurons (FS → PYR). Patch electrodes (3–4 MΩ) were filled with a solution containing (in mM): 117 mM KCl, 9 mM HEPES, 4 mM MgATP, 3 mM GTP, 20 mM creatine phosphate, 0.18 mM EGTA, and 0.3% biocytin, pH 7.3, 295 mOsm. GABAergic inhibitory postsynaptic currents (IPSCs) were generally recorded in the presence of bath applied DNQX (10 μM, Sigma, St Louis, MO) by generating timed action potentials in each presynaptic cell candidate (3 ms current pulse) while maintaining the postsynaptic neuron under voltage-clamp configuration at a holding potential (Vh) of −70 mV. Synaptic responses appeared under these recording conditions as inward currents. The magnitude of the GABAergic conductance was estimated by dividing the average IPSC by the liquid junction-corrected driving force (−75 mV). Inhibitory postsynaptic potentials (IPSPs) at resting potential were recorded while maintaining both the pre- and the postsynaptic cell under the current-clamp configuration. The connectivity via electrical synapses was tested by injecting prolonged pulses (500 ms) of hyperpolarizing current into each cell in turn and detecting a change in the membrane current of the electrically-coupled neuron. The amplitude of the electrical coupling conductance was measured by dividing the current produced in one cell by a voltage step in the coupled cell. We used power spectral analysis (Wavemetrics Igor: DSPPeriodogram) to determine the frequency of subthreshold membrane potential oscillations. The frequency of the subthreshold oscillations was indicated by a prominent peak in the power spectral plots (data not shown). The amplitude of the spikes and the amplitude of the afterhyperpolarization potentials (AHPs) were measured relative to the spike threshold. The duration of the AHP was estimated by calculating the time interval between half-amplitude points of the AHP (i.e., AHPt1/2). The voltage and current outputs were filtered at 5 kHz and digitized at 16-bit resolution (ITC-18, Instrutech, Port Washington, NY) with a sampling frequency of 10 kHz. The error due to the liquid junction potential was not corrected unless otherwise indicated. Access resistance of all recorded cells was not compensated and was monitored continually throughout each experiment; cells with a series resistance of <18 MΩ and <25% change for the duration of the experiment were used in our analysis.
Data are given as mean ± SEM. Statistical significance was tested using one-way ANOVA, Independent Student’s t test while the correlation coefficient (R) was calculated with linear regression. Differences were considered significant if p < 0.05. Data acquisition and analysis were performed using Igor software (Wavemetrics, Lake Oswego, OR).
To reveal the morphology of the recorded neurons, 0.3% w/v biocytin was included in the pipette recording solution. Following the physiological recordings, the tissue was processed using standard techniques to visualize the neurons with diaminobenzidine. The axons and dendrites of well-stained neurons were reconstructed in three dimensions using a Neurolucida system (Microbrightfield) and a ×100 oil-immersion objective (numerical aperture 1.4, Zeiss). No correction was made for tissue shrinkage.
To identify FS cells in L5/6 we selected fluorescent cells in a transgenic mouse line expressing EGFP in parvalbumin-positive fast-spiking cells (Chattopadhyaya et al., 2004). In this GAD67-GFP line (G42), the expression of GFP was detected as early as P0 and all GFP-positive cells became PV positive in the mature cortex (Chattopadhyaya et al., 2004). In the G42 line about 50% of parvalbumin cells also express EGFP (Chattopadhyaya et al., 2004). Thus the EGFP-expressing cells that we studied may represent a subset of the parvalbumin cells. Our recordings from FS cells at P3–6 showed that these cells display many of the characteristics of FS cells in adult cortex. Upon threshold current injections, FS cells at P3–6 exhibited high-frequency discharges similar to the spiking behavior typical of adult FS cells (Kawaguchi, 1997; Galarreta and Hestrin, 2002; Tateno et al., 2004) (Fig. 1 and Table 1). Repeating the same near-threshold current injection produced discharges exhibiting trial-to-trial variability which is also found in mature FS cells (Kawaguchi, 1997; Tateno et al., 2004; Towers and Hestrin, 2008) (Fig. 1A). Moreover, previous work has established that FS cells may produce prominent intrinsic subthreshold oscillations (Fig. 1B) (Tateno et al., 2004; Towers and Hestrin, 2008). Data obtained from recordings at P2–6 and P15–18 showed significant differences in the frequency of subthreshold membrane potential oscillations (see Methods). We found that in immature FS cells subthreshold oscillations had a range of 8–29 Hz (mean 19.3±1.3 Hz, n=11 cells; P2–6), while in more mature neurons the subthreshold oscillations had a range of 44–80 Hz (mean 61.5±2.6 Hz, n=12 cells; P15–18). Subthreshold oscillations were unaffected by synaptic neurotransmitter antagonists (DNQX and APV; data not shown). In addition we found that the duration of the AHP of P18 animals was shorter compared to that of P3 animals (Fig. 1C).
The membrane properties of FS cells progressively became more adult-like during the developmental time period that we studied (Table 1, Fig. 2). Figure 2A shows the respective values for all age groups normalized to P3–6, while Figure 2B displays the developmental change in the discharge frequency and the AHPt1/2 (n=15 cells per age group). We found that the input resistance (Ri) of FS cells decreased by 60% between P3–6 to P15–18 (Fig. 2C). The afterhyperpolarization (AHP) t1/2 became faster by an average of 50% between P3–18, which was paralleled by an increase of up to 100% in spike discharge frequency during this time frame (Fig. 2; A–C; table 1). Furthermore, we found that at P3–6 the mean resting potential (Vm) was more depolarized by an average of 16 mV compared to FS cells from older animals. Finally, spike half width of immature FS cells was about 6-fold longer compared to that in cells at P15–18 (Fig. 2C). Neurolucida tracings of FS cells at different age groups display relatively sparse arborization of dendrites and axons in immature cells (Fig. 2D).
It has been determined that in the somatosensory cortex the onset of feedforward inhibition onto spiny stellate cells in L4 occurs at P3–9 (Daw et al., 2007). However, the developmental onset of functional inhibition among inhibitory neurons in the cortex has not been directly studied. Moreover, whether electrical and GABAergic connections among inhibitory neurons appear at the same developmental stage has not been determined.
To address this question, we used simultaneous triple and paired whole cell recordings to evoke GABAergic responses from L5/6 FS interneurons between P3–18. We generated presynaptic action potentials with brief (2–3 ms) suprathreshold current injections in one FS cell and recorded the unitary responses from the other cells in an alternating pattern. Thus, we were able to test up to six directions from three pairs simultaneously. We recorded either unitary depolarizing inhibitory postsynaptic potentials (uIPSPs) under current clamp conditions (Fig. 3) or unitary hyperpolarizing inhibitory postsynaptic currents (uIPSCs) under voltage clamp conditions (Fig. 4).
When recording from FS cells at P3–4, we did not identify unitary GABAAR-mediated responses (n=0/8 pairs), and we only found one single functional GABAergic connection at P5 (n=1/13 pairs, Fig. 3A, D). At P6–7, synaptic connectivity was detected in 6 out of 31 pairs (19.4%). In the second postnatal week, we observed further increase in the rate of connectivity among FS cells. At P8–11 we found GABAergic connections in 16 out of 48 pairs (33.3%) and at P12–14, 12 out of 27 pairs (44.4%) were connected and at P15–18 we identified GABAergic connections in 9 out of 19 pairs (47.4%, Table 2; Fig. 3). Following the onset of GABAergic connections among FS cells, the probability of finding GABAergic connection was significantly correlated with the postnatal age (r=0.72, p<0.005, n=130 FS pairs tested; Fig. 3). Furthermore, we found that the functional maturation of newly formed inhibitory synapses was also associated with a significant developmental increase in the amplitude of unitary GABA-mediated conductance (Fig. 4E, Table 2). We found that the magnitude of the GABAergic conductance increased from 295.7 ± 39 pS at p6–7 to 701.6 ± 119 pS at p15–18 (Fig. 4E; Table 2).
Previous studies reported developmental changes in short term plasticity of inhibitory connections in the cerebellum (Pouzat and Hestrin, 1997). To test whether dynamics of GABAergic inhibition of FS cells change in the developing cortex, we estimated the paired-pulse ratio (PPR; Fig. 4 and Table 3). IPSCs among FS cells pairs exhibited short-term depression at all age groups (Fig. 4). However, for immature FS → FS, the PPR was significantly smaller compared to responses observed at P15–18 (0.62± 0.03 vs 0.91± 0.05, Fig. 4A, C).
This developmental increase of the PPR was accompanied by significant reduction in IPSC failure rate. Unitary FS → FS synapses at P6–7 exhibit a higher rate of failure compared to those of more mature FS cells, which rarely exhibited failures (21.2±5.7 % vs 0.9±0.01 %, Fig. 4B, D; Table 3).
In juvenile and adult rodents, FS cells are connected by both GABAergic and electrical synapses (Galarreta and Hestrin, 1999; Gibson et al., 1999; Galarreta and Hestrin, 2002). It has been suggested that electrical coupling may organize cortical circuits prior to the development of chemical synapses (Peinado et al., 1993a; Peinado, 2001; Montoro and Yuste, 2004; Sutor and Hagerty, 2005). However, so far the relative onset of GABAergic and electrical connections among inhibitory neocortical neurons has not been determined.
Thus, we next studied electrical coupling among FS cells during the first postnatal week (Fig. 5). To test for electrical coupling, we applied prolonged voltage steps (200 ms, 30 mV) to one of the potentially coupled FS cells while current deflections recorded in voltage-clamp mode indicated electrical coupling between these two neurons. In P3–5 animals we did not identify electrical coupling among FS → FS (0 out of 13 pairs). The earliest time point at which we observed functional electrical synapses was P6, when 5 out of 20 tested FS cell pairs (25%) were coupled (Fig. 5B, D). On average, we found an increase in coupling incidence up until P15–18. Electrical coupling was identified in 8 of 31 pairs of P6–7 animals (25.8%), while at P8–11 we found 16 out of 48 pairs (33.3%) to be coupled. By P15–18, coupling was detected in 8 out of 19 pairs (42.1%) (Fig. 5C, D).
In addition, we found that the strength of electrical coupling conductance increased 3-fold from 271.8 ± 16 pS at P6–7 to 837.2 ± 60 pS at P15–18 (Fig. 5E). Electrical coupling among FS → FS pairs was always bidirectional with similar conductance amplitude for both directions, although the coupling conductance varied significantly across different FS cell pairs.
Several FS → FS pairs were interconnected via both electrical and GABAergic synapses (data not shown). The probability of finding both types of connections increased with maturation. Only 3% of pairs were interconnected by both types of synapses at P6–7 while, at P15–18, 30% of cell pairs were mutually connected through both types of synapses. The probability of identifying GABAergic connections among electrically coupled pairs (40%; 16/40 pairs) was not significantly different than the probability of identifying GABAergic connections among all FS pairs tested (31.9%; 44/138 pairs).
Previous studies have shown that FS cells are not electrically coupled to pyramidal cells in juvenile (2–3 week old) or adult rodents (Galarreta and Hestrin, 1999; Gibson et al., 1999; Galarreta and Hestrin, 2002). However, it has been reported that FS cells can form electrical synapses with excitatory neurons in L2/3 of somatosensory cortex of P12–P14 mice (Venance et al., 2000; Meyer et al., 2002). In older animals (P28), this type of connection disappeared (Meyer et al., 2002). These data raise the possibility that the electrical coupling of FS cells is less selective in immature cortex as compared with that of adult. Thus, we examined electrical coupling of FS cells and pyramidal neurons in neonatal cortical layer V/VI. We performed simultaneous patch clamp recordings from two or three cells, testing a total number of 78 possible pairings between FS and pyramidal cells between P3 to P18. These data included 44 pairs at P3–P10. None of these pairs was found to be electrically coupled. We have also tested whether pyramidal cells are electrically coupled in immature cortex. However, we did not identify electrical coupling among the tested pairs of pyramidal cells (22 pairs at P3–10 and 11 pairs at P11–P18). Thus our data suggest that newly formed electrical synapses exhibit cell-type selectivity among FS cells.
To investigate whether the FS cell network is able to affect pyramidal neurons during the first postnatal week we recorded from pairs or triplets consisting of FS and pyramidal cells. Similar to GABAergic synapses among FS cells, we did not detect GABAergic signaling for FS → P pairs (0 connections of 5 pairs) in animals younger than P5 (Fig. 6A, D, Table 2). Inhibitory synapses were first detected at P6–7 in 6 out of 28 pairs (21.4%). By P8–11, we found that 7 out of 17 pairs (41.2%) were connected and at P15–18, 7 out of 14 FS → P pairs (50%) had established GABAergic synapses. Furthermore, we found that the newly formed inhibitory synapses exhibited developmental increase of the unitary conductance (Fig. 6E, Table 3). The mean increase was 4.2-fold from 155.3 ± 16 pS at P6–7 to 656.1 ± 83 pS at P15–18 (n=6 pairs per age group). We also estimated the PPR and failure rate of inhibition between FS and pyramidal cells (Fig. 6 and Table 3). We observed that FS → P pairs across all age groups exhibited short-term depression, evident by a decrease in the amplitude of the second IPSC. We did not find developmental change in PPR (0.46 ± 0.05% PPR at P6–7 compared to 96 ± 0.09% at P15–18; Fig. 6F, Table 3). However, we did observe significant reduction in IPSC failure rate during development. Unitary FS → P synapses at P6–7 exhibited a very high number of failures in contrast to those of more mature pairs, which rarely failed to respond (35.2 % failure rate at P6–7 compared to 4.0 % at P15–18; n=6 pairs tested per age group, Fig. 6G). These results suggest that the impact of FS cell inhibition on pyramidal cell firing could also be developmentally regulated. Taken together, our data indicate that pyramidal cell excitability is only weakly regulated by FS cell inhibition during very early development.
Our data support two main conclusions: First, we have shown that functional GABAergic connections among FS cells first appear at P5–6. Second, we demonstrated that electrical connections among FS cells appear at the same time as the GABAergic connections develop.
We found that at P3, FS interneurons are already able to respond to near threshold current injections with high frequency discharges and subthreshold membrane oscillations, which are characteristic electrophysiological patterns of adult FS cells (Kawaguchi, 1997; Tateno et al., 2004; Towers and Hestrin, 2008; Okaty et al., 2009). We observed significant developmental changes in membrane properties, such as an increase in the frequency of threshold discharges, a decrease in spike width and a three-fold decrease in the input resistance (Figure 2, Table 1). Similar findings have been recently shown by Okaty et al. who identified changes in both electrophysiological properties and expression patterns of ion channels in FS cells between P7 and P25 (Okaty et al., 2009).
Local GABAergic connections could play an important role in coordinating neuronal activity which in turn is thought to affect the organization of functional circuits in the developing cortex (Katz and Shatz, 1996; Ben-Ari, 2001; Ben-Ari et al., 2004; Adelsberger et al., 2005; Cang et al., 2005; Moody and Bosma, 2005; Hanganu et al., 2006). Extracellular stimulation has shown that functional GABAergic synapses are present in the neocortex in the first postnatal week (Luhmann and Prince, 1991; Agmon et al., 1996). The presynaptic elements generating GABA-mediated synaptic responses in the immature cortex may be cortical cells in layers 2–6 but could also include L1 neurons or ascending axons of inhibitory subplate cells and subcortical GABAergic axons (Schwartz et al., 1998; Dammerman et al., 2000b; Dammerman et al., 2000a; Dupont et al., 2006). A previous study showed that FS cells in L4 of somatosensory cortex form GABAergic connections with spiny stellate cells around P4 (Daw et al., 2007). However, the onset of GABAergic connections among FS cells has not been previously determined. Here, we found that GABAergic connections among L5/6 FS cells as well as between L5/6 FS cells and pyramidal cells first can be detected at P5 in the visual cortex of the mouse. Thus GABAergic connections among FS cells, between FS cells and pyramidal neurons in L5/6 and between FS cells and spiny stellate cells in L4 all appear at about the same developmental period. Furthermore, our data showed that the probability of identifying GABAergic synapses formed by FS cells increased during the next two postnatal weeks. In addition, both synaptic conductance and synaptic reliability increased during cortical maturation. Taken together, these data suggest that GABAergic synapses formed by FS cells do not contribute to coordinating cortical activity in the perinatal period (< P5). After P4–5, the probability of connection as well as the strength and reliability of the connections steadily increases suggesting that their influence on cortical activity increases during the second postnatal week. The decrease in the failure rate could be generated by increased probability of release or from an increase in the number of release sites among FS cells. However, an increase in PPR (Fig. 4B) suggests that the probability of release increases (Zucker and Regehr, 2002). Thus, our finding suggest that during development the number of synaptic contacts among FS cells increase as reflected in the increased probability of identifying connections and finding decrease in failure. We have not studied the mechanisms that underlie these changes. However, it is likely that increase in axonal and dendritic length results in increased overlap of axons and dendrites potentially generating more synaptic contacts. Developmental increase in the number of contacts among FS cells is also suggested by the increased conductances (Fig. 4E). However, we cannot rule out other mechanisms i.e., increase in the number of postsynaptic receptors.
It was previously shown that L5 parvalbumin-expressing GABAergic neurons are born early during embryogenesis (Butt et al., 2005; Cobos et al., 2005; Rymar and Sadikot, 2007) and that L5 is already populated with GABAergic neurons on the day of birth (Hevner et al., 2004). In agreement with these data, in the transgenic line we are using (G42), EGFP-positive cells are present at P0, and these EGFP-positive cells express parvalbumin in the adult neocortex (Chattopadhyaya et al., 2004). Here we showed that L5/6 FS cells in the visual cortex are not electrically coupled prior to P5. In addition we also showed that the magnitude of the conductance among electrically coupled pairs of FS cells is initially half of that we found in older animals. Moreover, we found no electrical coupling between FS cells and pyramidal neurons, suggesting that the process of synaptogenesis of electrical synapses is selective.
The factors controlling synaptogenesis of electrical connections among FS cells are not known. However, growth and maturation of dendrites is likely to be important (Chattopadhyaya et al., 2004). Moreover, studies of Cx36, which underlies electrical coupling among FS cells (Deans et al., 2001), have shown that Cx36 expression is sparse at birth and increases during development peaking at P14 (Belluardo et al., 2000) suggesting that expression of Cx36 may play a role in synaptogenesis of electrical synapses. Taking those data together with our physiological studies indicate that PV-FS cells are present in L5 after birth but do not form functional electrical synapses before P5. The onset of electrical coupling among a different type of inhibitory neuron, low-threshold spiking (LTS) cell, has not been previously determined. However, it was shown that the incidence of electrical coupling among neocortical LTS cells does not change between P8 to P15 (Long et al., 2005). These observations are generally similar to our finding (Fig. 5). It will be interesting to investigate when LTS cells form electrical synapses. Recent studies have found that inhibitory neurons in TRN are extensively electrically coupled in P1 mice and that the incidence of coupling does not change during maturation (Parker et al., 2009). In addition, it was reported that thalamic relay cells are connected by electrical synapses in P2 mice and that during maturation electrical coupling disappears (Lee et al., 2010). These data suggest that the developmental time course of electrical coupling varies among different brain regions.
Previous work has shown that the incidence of dye-coupling among neocortical neurons in rodents is high after birth and declines dramatically after P14 (Connors et al., 1983; Peinado et al., 1993b). These data can be interpreted as indication that electrical coupling is generally prevalent among different types of cortical neurons during the early postnatal period (Peinado et al., 1993a; Peinado, 2001; Montoro and Yuste, 2004; Sutor and Hagerty, 2005). However, without direct demonstration of electrical synapses quantitative interpretation of dye coupling experiments are difficult (Connors and Long, 2004; Wang et al., 2010). In juvenile and adult, FS cells have been shown to be extensively interconnected by gap junctions (Connors and Long, 2004; Hestrin and Galarreta, 2005). Our results, using paired recording, demonstrate that FS cells do not form electrical synapses before P5. In addition, we have not found electrical coupling among L5/6 pyramidal cells in immature animals. It is thus attractive to speculate that electrical coupling is rare among other types of cortical neurons in newborn mice. Further experiments using paired recording among other types of cortical neurons will resolve this issue. Interestingly, paired recordings have shown that a subset of subplate neurons are electrically coupled (Dupont et al., 2006). Taken together, these data suggest that electrical coupling plays a role in generating network activity in the subplate but not in the cortical layers of newborn animals.
We did not identify electrical or chemical synaptic interactions of FS cells before P5. These data indicate that the spatiotemporal patterns that are observed in the early postnatal days in mice are not generated by FS cells. We did not record from FS cells in layers 2–4. However, L5/6 develops before layers 2–4 and it is thus likely that FS cells in those layers do not contribute to patterned activity either. Several studies have shown that network activity in the developing neocortex changes around the end of the first postnatal week in rodents (Garaschuk et al., 2000; Dupont et al., 2006; Allene et al., 2008; Yang et al., 2009). Our data suggest that the synaptogenesis of both electrical and GABAergic connections of FS cells plays a role in the transition of network activity occurring at the end of the first postnatal week (Garaschuk et al., 2000; Moody and Bosma, 2005; Allene et al., 2008; Yang et al., 2009).
We thank Josh Huang for contributing the G42 line. We thank Solange Brown for comments on the manuscript. This project was supported by NEI and NARSAD grants (SH).