The adult hippocampus continuously generates new cohorts of immature neurons with increased excitability and plasticity. The window for the expression of those unique properties in each cohort is determined by the time required to acquire a mature neuronal phenotype. Here, we show that local network activity regulates the rate of maturation of adult-born neurons along the septotemporal axis of the hippocampus. Confocal microscopy and patch-clamp recordings were combined to assess marker expression, morphological development, and functional properties in retrovirally labeled neurons over time. The septal dentate gyrus displayed higher levels of basal network activity and faster rates of newborn neuron maturation than the temporal region. Voluntary exercise enhanced network activity only in the temporal region and, in turn, accelerated neuronal development. Finally, neurons developing within a highly active environment exhibited a delayed maturation when their intrinsic electrical activity was reduced by the cell-autonomous overexpression of Kir2.1, an inward-rectifying potassium channel. Our findings reveal a novel type of activity-dependent plasticity acting on the timing of neuronal maturation and functional integration of newly generated neurons along the longitudinal axis of the adult hippocampus.
The dentate gyrus of the adult hippocampus generates new dentate granule cells (DGCs) capable of information processing (Zhao et al., 2008). Adult neurogenesis is a complex process whereby neural progenitor cells adopt a neuronal fate, migrate, and mature over several weeks. During that period, young DGCs extend their axon and dendrites, establishing an appropriate input/output connectivity within the preexisting network (Ambrogini et al., 2004; Espósito et al., 2005; Overstreet-Wadiche et al., 2005, 2006a; Ge et al., 2006; Laplagne et al., 2006; Piatti et al., 2006; Toni et al., 2007, 2008). Interestingly, immature DGCs exhibit reduced GABAergic inhibition, high excitability, and a lower threshold for the induction of long-term potentiation (Wang et al., 2000; Snyder et al., 2001; Schmidt-Hieber et al., 2004; Espósito et al., 2005; Overstreet-Wadiche et al., 2005; Ge et al., 2006, 2007; Markwardt et al., 2009; Mongiat et al., 2009). Such high excitability allows them to spike despite their incipient glutamatergic inputs. Therefore, immature DGCs might participate in information processing before reaching a fully mature stage. After reaching maturity, their excitability decreases and they acquire a degree of functional connectivity and plasticity that is similar to that of all preexisting DGCs (Laplagne et al., 2006, 2007). Thus, new cohorts of immature DGCs with unique functional properties are continuously generated. The duration and the impact of those distinctive functional properties in the dentate gyrus network will depend on the speed of maturation of new DGCs.
The most well characterized regulatory steps of adult hippocampal neurogenesis are the rate of progenitor cell proliferation and the survival rate of new DGCs. For instance, exercise, learning, and enriched environment can increase neurogenesis, whereas aging, stress, and depression decrease it (Gould et al., 1999; van Praag et al., 1999; Parent and Lowenstein, 2002; Abrous et al., 2005; Zhao et al., 2008). These physiological stimuli primarily affect proliferation or survival. The notion that neuronal maturation can be altered was first highlighted by epileptic seizures, in which new DGCs showed mature features during early development (Overstreet-Wadiche et al., 2006b). Chronic antidepressant treatments were also shown to stimulate neuronal maturation (Wang et al., 2008). In addition, experimental manipulations that altered GABA signaling in new DGCs induced remarkable defects in their development (Ge et al., 2006). Those previous works involving a pathological condition or a specific alteration in GABA signaling showed that neuronal development is sensitive to altered activity. However, whether the timing of maturation of newborn DGCs can be regulated by changes that occur within a physiological range of neuronal activity remains unknown.
The rodent hippocampus displays a longitudinal axis bending from the septal nuclei rostrodorsally toward the temporal lobe in the caudoventral area (see Fig. 1A) (Amaral and Witter, 1989). Despite the lack of anatomically defined regions, the patterns of anatomical connectivity and gene expression support a compartmentalization of the hippocampus along its longitudinal (septotemporal) axis (Verwer et al., 1997; Dolorfo and Amaral, 1998; Petrovich et al., 2001; Thompson et al., 2008; Fanselow and Dong, 2010). Consistently, distinct behaviors involve different areas of the hippocampus (Bast and Feldon, 2003; Bannerman et al., 2004). The septal to intermediate hippocampus receives connections from the dorsolateral entorhinal cortex and it is primarily associated to spatial learning (Moser et al., 1995; Fyhn et al., 2004). The temporal to intermediate hippocampus, via connections to medial prefrontal cortex and subcortical sites such as the amygdala and hypothalamus, is linked to anxiety and emotional state (Kjelstrup et al., 2002). Finally, the intermediate region exhibits overlapping characteristics with its neighbors and it has been involved in functional translation of rapid place learning to behavioral performance (Bast et al., 2009). In this context, the adult dentate gyrus itself may present different neurogenic environments for neuronal maturation. Interestingly, recent studies have revealed that the granule cell layer (GCL) of the septal pole of the dentate gyrus displays higher levels of basal neuronal activity than the remaining GCL. Moreover, the density of newborn neurons is also higher in the septal dentate gyrus (Snyder et al., 2009a,b; Jinno, 2011). Here, we demonstrate that those regional differences in basal activity can act as endogenous regulators of the rate of neuronal maturation.
Materials and Methods
Production of viral vectors.
We used a retroviral vector based on the Moloney murine leukemia virus (Laplagne et al., 2006). Retroviral particles were assembled using three separate plasmids containing the envelope (CMV-vsvg), viral proteins (CMV-gag/pol), and transgenes. Transgenes included a fluorescent reporter such as GFP or RFP, mouse Kir2.1 (a gift from G. Lanuza, Instituto de Biología y Medicina Experimental, Buenos Aires, Argentina), or the nonconductive mutant KirNC under CAG or PGK promoters. KirNC was obtained by replacing residues G144Y145G146 to AAA in Kir2.1 using site-directed mutagenesis (Burrone et al., 2002). Kir or KirNC sequences were followed by an internal ribosome entry site (IRES) and a fluorescent reporter (CAG-Kir-IRES-GFP and CAG-KirNC-IRES-RFP). Plasmids were transfected into 293T cells using deacylated polyethylenimine. Virus-containing supernatant was harvested 48 h later and concentrated by two rounds of ultracentrifugation. Virus titer was typically ∼105 particles/μl. For the coinfection experiments shown in Figure 7D (see below), we used a mixture of CAG-RFP and CAG-Kir-IRES-GFP retroviruses in a 1:5 ratio.
Subjects and stereotaxic surgery for retroviral delivery.
Female C57BL/6 mice, 6–7 weeks of age, were housed at four to five mice per cage in standard conditions or with two running wheels as indicated. Running wheel housing started 3 d before surgery and continued for the duration of the experiment. Mice were anesthetized (150 μg ketamine/15 μg xylazine in 10 μl of saline per gram) and virus (1 μl at 0.15 μl/min) was infused into the right dentate gyrus using sterile microcapillary calibrated pipettes (Drummond Scientific) and stereotaxic surgery [coordinates: −2 mm anteroposterior (AP), −1.5 mm lateral (L), −1.9 mm ventral (V)]. A single injection site was sufficient to label a substantial number of neural precursor cells throughout the septotemporal axis of the hippocampus. In electrophysiology experiments shown in Figure 2, stereotaxic coordinates were optimized to deliver the virus to the septal (−1.9 AP, −1.7 L, −1.8 V) or the temporal dentate gyrus (−2.4 AP, −2.6 L, −2.1 V). Animals were killed at the indicated times [14, 18, 21, 35, or 56 d postinfection (dpi)] for immunofluorescence or at 14, 21, 28, 35, or 42 dpi for electrophysiological recordings.
Bromodeoxyuridine and Arc labeling.
Bromodeoxyuridine (BrdU) (Sigma-Aldrich) was dissolved in 0.9% NaCl and was delivered intraperitoneally at a dose of 50 μg/g to mice housed under standard conditions to label dividing cells. To assess neuronal phenotype of labeled progenitors (experiments shown in Fig. 2D), mice received two injections per day over 2 d and were killed 21 d later. To measure the proportion of cells that continue to proliferate after labeling (see Fig. 3), 10 mice were injected three times in a single day (once every 6 h) to label different pools of neural progenitor cells. Mice were killed 2 and 4 d later to assess colabeling with Ki67 (see below). For Arc immunofluorescence, running and sedentary mice were maintained in the appropriate housing conditions (sedentary or running) from 6 to 7 weeks of age and were killed 24 d later to match the timing of retroviral experiments done at 21 dpi.
Immunostaining was done on 40 or 60 μm free-floating coronal sections throughout the fixed brain, analyzing up to one every six sections to obtain ≥13 GFP+ or BrdU+ cells to each DG region per mouse. Antibodies were applied in TBS with 3% donkey serum and 0.25% Triton X-100. Double- or triple-labeling immunofluorescence was performed using the following primary antibodies: Arc (rabbit polyclonal; 1:500; Synaptic Systems), BrdU (rat monoclonal; 1: 200; Abcam), calbindin D-28k (rabbit polyclonal; 1:1000; Swant), doublecortin (DCX) (rabbit polyclonal; 1:750; a gift from C. Walsh, Harvard Medical School, Boston, MA), GFP (rabbit polyclonal; 1:100; Invitrogen; or chicken polyclonal; 1:500; Millipore; or chicken polyclonal; 1:500; Aves), Ki67 (rabbit monoclonal; 1:250; Vector Laboratories), NeuN (mouse monoclonal; 1:50; a gift from F. H. Gage, Salk Institute for Biological Studies, La Jolla, CA), and RFP (rabbit polyclonal; 1:200; Millipore Bioscience Research Reagents). For calbindin (Cb) immunolabeling, preincubation with methanol (15 min) was included to enhance penetrability. The following corresponding secondary antibodies were used: donkey anti-mouse Cy5, donkey anti-rabbit Cy3, donkey anti-chicken Cy2 (1:250; Jackson ImmunoResearch). Although inflammation was minimal because of the thin capillary pipettes used for stereotaxic injections, we used GSA (1:100; Vector Laboratories) and streptavidin Cy5 (1:200; Jackson ImmunoResearch) immunostaining to determine the spread of inflammation produced by the surgery and viral infection and avoid phenotypic and morphological analysis in these conditions.
For BrdU detection, DNA was denatured with 50% formamide in 2× SSC buffer at 65°C for 2 h, washed in 2× SSC for 10 min, incubated in 2N HCl at 37°C for 30 min, and washed in 0.1 m boric acid, pH 8.5, for 10 min. For double labeling with the cell cycle marker Ki67 and BrdU, we used a serial protocol without formamide to avoid unspecific Ki67 labeling. Sections were first incubated with Ki67 antibody (4°C; overnight), fixed with paraformaldehyde 4% for 15 min, treated with 2N HCl for 20 min at room temperature, 0.1 m boric acid for 10 min, washed, and followed by BrdU antibody incubation (4°C; overnight).
Anatomical definitions, confocal microscopy, and image analysis.
Regions that are denominated septal and temporal in this study correspond, respectively, to sections containing the dorsal-anterior hippocampus (bregma, −0.9 to −1.8 mm) and the dorsal-posterior (intermediate) and ventral region of the hippocampus (bregma, −2.7 to −3.88) according to the mouse brain atlas of Paxinos and Franklin (1997).
Images were acquired using a Zeiss LSM 5 Pascal or a Zeiss LSM 510 Meta confocal microscopes (Zeiss). Only GFP+ or BrdU+ cells located in the subgranular zone (<20 μm thick) or GCL were included in the analysis. Colocalization of fluorescent markers was assessed in three-dimensional reconstructions through Z-stacks using multiple planes for each cell. Reconstructions included the entire cell soma for Cb, NeuN, BrdU, and Ki67, and the cell soma plus the first 30 μm of apical dendrites for DCX, as shown in the overlays depicted in Figure 2, A and B. Images were taken at 1 μm intervals using an optical slice of 0.7–1 μm corresponding to an airy unit of 1 for each fluorophore [40× oil-immersion objective; numerical aperture (NA), 1.4; digital zoom of 2].
Arc expression was assessed from x–y projections from confocal z-series. We calculated the proportion of DGCs expressing Arc as follows: (1) the area of the GCL was measured in septal and temporal sections and the number of Arc+ cells was counted to obtain the density of Arc+ cells; (2) the density of NeuN+ cells per square millimeter was sampled in septal and temporal sections to correct for the angle in coronal sections and the volume of DGC somas in each region (Bayer, 1982) (17,800 ± 900 and 12,700 ± 900 cells/mm2, respectively); (3) the ratio Arc+ cells/number of NeuN+ was calculated.
For spine counts, we selected GFP+ dendritic segments located in the middle third of the molecular layer. High-resolution images were acquired using a 63× objective (NA, 1.4; oil-immersion) and taking z-series of 40–200 optical slices of airy unit = 1 at 0.1 μm intervals as previously described (Morgenstern et al., 2008). All dendritic spines within 2 μm from the shaft were counted on projections onto a single plane. Four to 9 dendritic segments (40–50 μm in length) were imaged per dentate gyrus region per mouse, choosing fragments at a distance ≥150 μm from each other to avoid sampling multiple dendrites from single neurons. A similar number of fragments were chosen from the infrapyramidal and suprapyramidal blades for each area. In all cases, dendrites with high fluorescence intensity were selected to minimize counting errors because of insufficient signal. For dendritic length measurements shown in Figure 7C–E, images were acquired (40×; NA, 1.3; oil-immersion) from 60-μm-thick sections taking z-series including 35–50 optical slices, airy unit = 1 at 0.8 μm intervals. The Kir-IRES-GFP retrovirus rendered low fluorescence intensity that was insufficient for dendritic measurements. To solve that problem, dendritic trees of Kir-expressing neurons were characterized after coinfection with two retroviruses (Fig. 7D): a Kir-IRES-GFP construct (which allowed identifying the soma of Kir neurons) and a CAG-RFP construct (which rendered high fluorescence in soma and processes). Dendritic length was measured from projections of three-dimensional reconstructions onto a single plane using Zeiss LSM image Browser software.
Three-dimensional reconstructions of dendrites quantified in Figure 1D were performed in 400-μm-thick vibratome coronal sections. Slices were fixed (4% paraformaldehyde) and mounted. Images were taken using a Zeiss LSM 710 NLO multiphoton microscope, a 20× water-immersion objective (NA, 1.0), and a Chameleon Ultra II pulsed laser (Coherent). Series of 200–400 optical slices were acquired at 1 μm intervals. Dendritic length was measured from the three dimensional reconstructions using the ZEN 2009 software (Carl Zeiss).
Mice were anesthetized and decapitated at 14, 21, 28, 35, or 42 dpi as indicated. Brains were removed into a chilled solution containing the following (in mm): 110 choline-Cl−, 2.5 KCl, 2.0 NaH2PO4, 25 NaHCO3, 0.5 CaCl2, 7 MgCl2, 20 dextrose, 1.3 Na+-ascorbate, 0.6 Na+-pyruvate, and 4 kynurenic acid. Horizontal slices (400 μm thick) were cut in a vibratome (Leica VT1200 S) and transferred to a chamber containing the following (in mm): 125 NaCl, 2.5 KCl, 2 NaH2PO4, 25 NaHCO3, 2 CaCl2, 1.3 MgCl2, 1.3 Na+-ascorbate, 3.1 Na+-pyruvate, and 10 dextrose (315 mOsm). Slices were bubbled with 95% O2/5% CO2 and maintained at 30°C for >1 h before experiments started. Whole-cell recordings were performed at 23 ± 2°C using microelectrodes (4–6 MΩ) pulled from borosilicate glass (KG-33; King Precision Glass) and filled with the following (in mm): 120 K-gluconate, 20 KCl, 5 NaCl, 4 MgCl2, 0.1 EGTA, 10 HEPES, 4 Tris-ATP, 0.3 Tris-GTP, 10 phosphocreatine, Alexa Fluor 594 (5 μg/ml; Invitrogen), pH 7.3, and 290 mOsm. For mIPSC recordings, electrodes were filled with a similar solution, except for the following (in mm): 19 K-gluconate, 121 KCl, 5 NaCl, 4 MgCl2, 0.1 EGTA. Recordings were obtained using an Axopatch 200B amplifier (Molecular Devices), digitized (Digidata 1322A), and acquired at 20 kHz onto a personal computer using the pClamp 9 software (Molecular Devices). Membrane capacitance and input resistance were obtained from current traces evoked by a hyperpolarizing step of 10 mV. In current-clamp recordings, the resting membrane potential was kept at −70 mV by passing a holding current. The threshold current for spiking was assessed by successive depolarizing current steps (5 pA; 200 ms) to drive the membrane potential from resting to 0 mV. Voltage-dependent Na+ and K+ currents were measured after leak subtraction using a p/6 protocol and automatic detection of the fast inward peak and the late outward plateau. Kir currents were measured as the steady-state inward deflection in response to hyperpolarizing voltage steps (from −130 to −90 mV). Kir conductance was calculated after subtracting the leak conductance measured between −60 and −40 mV, where Kir channels are closed (Mongiat et al., 2009). Spontaneous postsynaptic excitatory currents (sEPSCs) were recorded at a holding potential of −70 mV, in the presence of picrotoxin (100 μm) and (2S)-3-([(1S)-1-(3,4-dichlorophenyl)ethyl]amino-2-hydroxypropyl)(phenylmethyl)phosphinic acid (CGP55845) (100 nm). Miniature EPSCs (mEPSCs) and miniature IPSCs (mIPSCs) were recorded in the presence tetrodotoxin (0.5 μm) and CGP55845 (100 nm), and picrotoxin (100 μm; for mEPSCs) or kynurenic acid (4 mm; for mIPSCs). Criteria to include cells in the analysis were colabeling with Alexa Fluor 594 or visual confirmation of GFP in the pipette tip, and absolute leak current <50 pA at −70 mV. Series resistance was typically 10–20 MΩ, and experiments were discarded if >30 MΩ.
Statistics used throughout the manuscript are described in the figure legends and in the text. All comparisons between neuronal populations involving the septal and temporal hippocampus of the same mice were done using paired analysis. When data met normality tests (Gaussian distribution and equal variance), two-tailed t tests or ANOVA were used, as indicated. In cases in which data did not meet normality criteria, nonparametric tests were used as follows: Mann–Whitney test for independent comparisons, Wilcoxon's test for simple paired comparisons, Kruskal–Wallis test for multiple comparisons, and Dunn's or Conover's test as post hoc analysis.
Adult-born DGCs from the same cohort exhibit different degrees of maturation along the septotemporal axis of the hippocampus
The anatomical and functional gradients along the hippocampal axis might entail differences in neuronal development. We first investigated possible differences for immature neurons of the same cohort between the septal and temporal region of the hippocampus of sedentary mice. To address this question, dividing neural progenitor cells were labeled in the dentate gyrus of 6- to 7-week-old mice by injecting a retrovirus that expresses GFP (Laplagne et al., 2006). GFP+ neurons were characterized 21 dpi, a critical neuronal age that is coincident with a high rate of glutamatergic synaptogenesis (Espósito et al., 2005; Ge et al., 2006; Zhao et al., 2006). Interestingly, new DGCs developing in the septal hippocampus displayed a larger and more elaborated dendritic tree than neurons from the same cohort developing in the temporal region (Fig. 1A,B). Dendritic length of 21 dpi neurons was then measured using two-photon microscopy in 400-μm-thick sections to obtain a complete reconstruction of the dendritic tree. A significantly longer dendritic tree was visualized in newborn cells of the septal region compared with those developing in the temporal area (Fig. 1D). Since network activity is different along the longitudinal axis of the hippocampus under basal conditions (Jung et al., 1994; Snyder et al., 2009a,b), we assessed the expression of the immediate early gene Arc as a sensor for neuronal activity in the entire GCL of the septal and temporal dentate gyrus (Chawla et al., 2005; Ramirez-Amaya et al., 2006; Vazdarjanova et al., 2006; Kee et al., 2007). The overall number of active DGCs was low, consistent with the sparse coding of the dentate gyrus (Chawla et al., 2005; Leutgeb et al., 2007); yet substantial differences between hippocampal areas were observed (Fig. 1C,E). Arc immunofluorescence was detected in ∼2.7% of septal DGCs and <1% of temporal DGCs, which reflects a higher level of basal activity in the septal dentate gyrus, in agreement with recent works (Snyder et al., 2009a,b). Remarkably, the higher proportion of Arc-expressing (Arc+) neurons in the septal area was observed in all tested mice, highlighting a very robust difference in the levels of network activity in the longitudinal axis of the dentate gyrus. These results suggest that young DGCs from the same cohort exhibit a highly elaborated morphology in the more active region (septal) of the adult dentate gyrus.
To assess whether the distinct morphologies described above reflect true differences in the degree of maturation of newborn DGCs in local environments of the hippocampus, we measured the proportion of GFP+ neurons expressing DCX, a microtubule-associated protein present during neuronal migration that is commonly used to label immature neurons (Espósito et al., 2005). NeuN was used as a constitutive neuronal marker and counterstain for the GCL. At 21 dpi, DCX expression was observed in ∼50% of GFP+ neurons at the septal dentate gyrus but in >90% of newborn DGCs at the temporal region (Fig. 2A–C). The remaining GFP+ cells expressed only NeuN (DCX−), which confirms their neuronal phenotype. Therefore, migration has been completed in ∼50% of newborn DGCs in the septal hippocampus, but in only ∼10% of DGCs developing in the temporal region. Septotemporal differences in neuronal maturity at 3 weeks were further confirmed by labeling dividing progenitor cells by systemic delivery of BrdU, a noninvasive labeling technique (Fig. 2D). This experimental condition rendered a similar pattern to that obtained with retroviral labeling, with higher DCX expression in newborn cells of the temporal hippocampus. Together, these results demonstrate that DGCs born at the septal pole of the hippocampus achieve a more mature neuronal phenotype in 3 weeks than those generated at the temporal region.
To determine whether the observed differences in the pattern of expression of neuronal markers also implicate neuronal physiology and connectivity, electrophysiological properties of adult-born DGCs were studied at 21 dpi. Whole-cell recordings were performed in GFP+ neurons in acute slices obtained from the septal and temporal areas of the hippocampus. Recordings from GFP+ DGCs of the septal hippocampus revealed a lower input resistance (Rinput) than those from temporal GFP+ DGCs (Rinput = 636 ± 94 MΩ, n = 25 for septal; 1900 ± 420 MΩ, n = 24 for temporal; p = 0.007, t test), typical of a more advanced degree of maturation. New DGCs of the septal region also showed more mature firing properties as seen by the larger amplitude of voltage-gated Na+ and K+ currents and the repetitive spiking elicited by depolarizing current steps (Fig. 2E,F). The maximum Na+ and K+ conductances were 344 ± 31 and 53.6 ± 4.9 nS (n = 16 for septal), and 148 ± 29 and 27.1 ± 5.3 nS (n = 14 for temporal DGCs; p < 0.0001 for Na+; p = 0.001 for K+, t test). Finally, the frequency but not the amplitude of sEPSCs was significantly higher in septal newborn DGCs (∼1 vs ∼0.2 Hz), reflecting a higher degree of afferent glutamatergic connectivity than the temporal newborn DGCs (Fig. 2G–I). Therefore, all of the assessed functional properties indicate that new DGCs developing at the septal pole of the adult hippocampus are ready to participate in information processing at a time when new DGCs of the same cohort in the temporal region are still highly immature and poorly integrated in the preexisting circuitry.
Slower rate of neuronal maturation in the temporal dentate gyrus
The differences in the degree of neuronal maturation described above could be compatible with the following scenarios: (1) progenitor cells in the temporal dentate gyrus continue to proliferate and exit the cell cycle at a later time, beginning their maturation only after a certain delay; (2) neurons developing in the temporal region are stalled at immature stages and fail to reach a fully mature phenotype; (3) maturation occurs at different rates along the longitudinal axis of the adult hippocampus. A series of experiments were performed to discriminate between these possibilities.
We first analyzed possible septotemporal differences in the time at which neural progenitor cells abandon the cell cycle. To address this issue, we injected BrdU for 1 d to label dividing cells of the subgranular zone, and evaluated the proportion of those cells that continue to proliferate at later times. The cell cycle marker Ki67 was used to identify cells that continue to divide 2 and 4 d after BrdU injection. Consistent with previous observations, ∼30% of the dividing cells were still proliferating (BrdU+/Ki67+) in the whole dentate gyrus 2 d after BrdU injection. Moreover, the density of new cells (BrdU+) at 2 d was higher in the septal dentate gyrus by 33.1 ± 14.0% when compared with the temporal region (p = 0.032, paired t test) (Dayer et al., 2003; Snyder et al., 2009a,b; Jinno, 2011). However, no differences in the proportion of cells that were still proliferating (BrdU+/Ki67+) were found at 2 or 4 d after BrdU injections in the septal versus temporal regions (∼30 and ∼15%) (Fig. 3). These results indicate that both pools of neural progenitor cells exit the cell cycle at the same time. Therefore, the observed differences in the development of septal and temporal DGCs are not attributable to a dissimilar onset of neuronal differentiation.
We then compared morphology and expression of neuronal markers of newborn DGCs in the septal and temporal hippocampus at 21 and 56 dpi to address whether new DGCs of the temporal region fail to reach a fully mature phenotype. For these experiments, we selected 56 dpi as the time when adult-born DGCs have already completed their maturation (Espósito et al., 2005; Laplagne et al., 2006; Zhao et al., 2006). Despite the fact that 21 dpi neurons showed profound septotemporal differences, all new neurons displayed similar features by 56 dpi (Fig. 4A–D). Since the highest rate of dendritic spine formation in adult-born DGCs occurs by the third week, we measured spine density as a high-resolution parameter that accurately reflects the degree of maturation. By 21 dpi, DGCs developing at the septal hippocampus displayed a rather mature phenotype with spiny dendrites (∼1.5 spines/μm) spanning the entire molecular layer (Fig. 4A,E,G). At 56 dpi, new neurons in this area showed a marked increase in spine density (∼2.5 spines/μm) but maintained their overall mature features (Fig. 4C,F,G). In striking contrast, 21 dpi neurons in the temporal region displayed simple thin dendrites restricted to the middle molecular layer, dendritic varicosities, low spine density (∼0.8 spines/μm), and basal dendrites projecting to the hilus, all typical properties of an immature dendritic tree (Figs. 4B,E,G, 1D) (Jones et al., 2003). These results are in agreement with the electrophysiological recordings described above displaying immature intrinsic properties and reduced glutamatergic connectivity onto temporal DGCs (Fig. 2). However, neuronal maturation in the temporal region displayed a clear progress by 56 dpi, reflected by both a qualitative change in morphology and a significant increase in spine density (Fig. 4D,F,G). Therefore, by 56 dpi, all new neurons were equally and completely mature, displaying a round soma, conspicuous axonal fibers extending toward the hilus, and dendrites spanning the molecular layer with a high spine density characteristic of mature DGCs (Trommald and Hulleberg, 1997; Zhao et al., 2006). These observations argue against the possibility that temporal newborn cells fail to reach complete maturation.
Finally, to strengthen the finding that new septal DGCs mature faster than new temporal DGCs, we monitored two parameters that reflect the phenotypic and physiological aspects of neuronal development. We first studied the time course of Cb expression, which is a specific neuronal marker commonly used to identify the latest stages of development in adult-born DGCs (Zhao et al., 2008). Although Cb immunoreactivity was detected in few neurons (<10%) in both the septal and temporal dentate gyrus at 14 dpi, a striking increase in Cb expression to almost plateau levels occurred only in the septal DGCs at 21 dpi (Fig. 4H–J). By 28 dpi, most DGCs displayed Cb expression regardless of their longitudinal position, suggesting that all new neurons have entered their latest stages of maturation. However, although Cb is usually considered as a mature neuronal marker, it seems to be expressed in developing DGCs that have not yet reached functional and morphological maturity (Espósito et al., 2005; Piatti et al., 2006; Toni et al., 2008; Zhao et al., 2008). Since membrane properties display reliable changes as neurons progress along different stages of maturation (Espósito et al., 2005; Piatti et al., 2006), we compared Rinput between new DGCs developing in the septal and temporal hippocampus (Fig. 4K). Although septal DGCs displayed an abrupt decline in Rinput between 14 and 21 dpi, temporal DGCs exhibited a more gradual decrease in the examined interval. Notably, Rinput measurements revealed striking differences at 28 dpi (667 ± 67 MΩ for septal and 1400 ± 240 MΩ for temporal DGCs), whereas Cb expression had reached similar values in septal and temporal DGCs (Fig. 4J). Rinput values typical of mature DGCs were found in new neurons of both regions by 42 dpi (379 ± 44 MΩ for septal and 440 ± 78 MΩ for temporal DGCs). These results highlight the lengthened interval during which newborn DGCs of the temporal hippocampus maintain immature functional properties. Based on marker expression, morphology, electrophysiological properties, and connectivity, we conclude that neuronal maturation progresses at a faster rate at the septal compared with the temporal region of the adult dentate gyrus.
Enhanced network activity by voluntary exercise accelerates neuronal maturation
To investigate how neuronal activity of the local environment impinges in the rate of neuronal maturation, we sought for physiological means to modulate circuit activity. Network activity in the hippocampus is coupled to voluntary locomotion (Vanderwolf, 1969; Foster et al., 1989). For instance, the firing rate increases with running speed in different longitudinal regions of the hippocampus (Czurkó et al., 1999; Maurer et al., 2005). We therefore explored the effects of long-term running on the level of basal activity in the GCL. Interestingly, running did not modify the proportion of active (Arc+) DGCs in the septal region, but, in contrast, it did produce a substantial increase (>150%) in the proportion of Arc+ DGCs in the temporal region (Fig. 5A,B). This specific change in neuronal activity by running equalized the proportion of active DGCs in the septal and temporal hippocampus (Fig. 5C).
We then compared the degree of maturation of 3-week-old neurons in the septal and temporal hippocampus of sedentary and running mice. We first observed a conspicuous increase in the number of GFP+ neurons (Fig. 5D), consistent with the well known enhancing effect of voluntary exercise on the rate of progenitor cell proliferation (van Praag et al., 1999). Most strikingly, newborn DGCs at 21 dpi displayed mature features in both hippocampal regions, such as dendritic trees spanning the entire molecular layer, a round soma, and absence of basal dendrites. At higher magnification, we observed thicker dendritic processes coated with spines in both regions of the dentate gyrus, and the conspicuous varicosities observed in the temporal area of sedentary mice were no longer present in running mice (Fig. 5E). Accordingly, a significant increase in spine density was induced by running exclusively in new DGCs of the temporal region (Fig. 5F). In agreement with these results, the regional differences in Cb expression at 21 dpi were also equalized by running. The proportion of newborn DGCs labeled with Cb was not modified by running in the septal area, but it displayed a threefold increase (to ∼75%) in the temporal region (Fig. 5G,H). These observations demonstrate that voluntary exercise can accelerate the rate of neuronal development specifically in the temporal dentate gyrus. In these conditions, maturation of newborn DGCs in the septal and temporal hippocampus occurs at similar rates.
A critical role for intrinsic activity on neuronal maturation
The experiments presented above highlight a correlation between the level of activity in the neurogenic niche and the rate of neuronal development and functional integration. We next evaluated whether there is a causal link between electrical activity and neuronal maturation. To test whether neuronal activity can directly modulate neuronal maturation, excitability of newborn DGCs was decreased by retroviral delivery of the inward rectifier K+ channel Kir2.1. Retrovirally labeled neurons expressing GFP (control) or a mutant Kir2.1 with a nonconductive pore (KirNC) were used as controls. Electrophysiological recordings confirmed that 21 dpi neurons overexpressing Kir (but not KirNC) displayed larger inward rectifier currents (approximately threefold increase), decreased input resistance, hyperpolarized resting potential, and diminished levels of subthreshold depolarization (Fig. 6). These results demonstrate that Kir overexpression can efficiently reduce the excitability of developing DGCs.
Phenotypic effects of a decrease in the intrinsic activity of developing neurons were analyzed at the morphological and physiological level. These experiments were performed in running mice to equalize basal activity at the maximal level for both the septal and temporal regions. New neurons overexpressing Kir almost doubled DCX expression at 21 dpi and displayed reduced Cb levels between 14 and 21 dpi when compared with control DGCs (Fig. 7A,B). Notably, Cb immunoreactivity in 21 dpi neurons expressing KirNC was similar to control DGCs (Fig. 7B, inset), indicating that the phenotypic defect induced by Kir is specific to the reduced excitability. At 35 dpi, DCX was absent and Cb expression was maximal in Kir and control new neurons, indicating that Kir neurons have reached a mature pattern of marker expression. These results demonstrate that reduced intrinsic excitability delayed the rate of newborn cell maturation in a highly active environment.
In addition to the delayed expression of early and late markers, Kir neurons displayed short dendrites at 21 dpi, also consistent with a more immature neuronal stage (Fig. 7C–E). This morphological difference was still present at 35 dpi, highlighting an additional delay that is maintained beyond the timing required for Cb expression. To determine whether the diminished dendritic length is reflected at the level of neuronal connectivity, we performed recordings of mEPSCs and mIPSCs. New DGCs expressing Kir displayed lower frequency of both mEPSCs and mIPSCs than control cells with little or no differences in amplitude, reflecting poor afferent connectivity (Fig. 8A–C). Finally, new neurons expressing Kir (but not KirNC) evidenced a striking reduction in cell membrane capacitance (Cm), a parameter that is proportional to the area of the neuronal membrane (Fig. 8D). The smaller Cm in Kir neurons is also consistent with a more immature stage of development (Espósito et al., 2005). These observations indicate that intrinsic excitability regulates the maturation of newborn DGCs in the adult hippocampus. We conclude that electrical activity in the neurogenic niche plays a crucial role in the timing required for neuronal maturation.
Developing DGCs of the adult hippocampus undergo well defined transitions in morphology, excitability, and connectivity in the pathway toward a fully mature phenotype (Ambrogini et al., 2004; Espósito et al., 2005; Overstreet-Wadiche et al., 2005, 2006a; Ge et al., 2006; Laplagne et al., 2006; Piatti et al., 2006; Zhao et al., 2006; Toni et al., 2007, 2008). Among those transitions, there is a window for the expression of unique properties that establishes newborn DGCs as a distinctive functional population within the adult dentate gyrus (Wang et al., 2000; Snyder et al., 2001; Schmidt-Hieber et al., 2004; Ge et al., 2007; Mongiat et al., 2009). In addition, the view that the hippocampus contains heterogeneous niches for adult neurogenesis is now clearly emerging. Recent studies have shown that larger pools of newborn DGCs are generated in the septal region of the adult dentate gyrus compared with the temporal pole (Tashiro et al., 2007; Snyder et al., 2009a,b; Jinno, 2011). Such septotemporal differences in neurogenesis are most likely attributable to higher rates of progenitor cell proliferation or neuronal survival in the more active septal area. In this work, we demonstrate that the hippocampus also contains heterogeneous domains in regard to the rate of neuronal maturation, with the septal and temporal areas exhibiting different features. Our experiments in sedentary mice reveal that newborn DGCs are ready to participate in information processing in the septal hippocampus at a time when same-cohort neurons of the temporal region are still highly immature and poorly connected. Moreover, the septotemporal difference in the timing of neuronal maturation described in this study predicts a shorter period of enhanced excitability in the septal dentate gyrus. This functional polarization of the hippocampus is tightly associated to differences in the basal level of activity in the local environment. We also show that running increases local activity and, consequently, accelerates neuronal maturation only in the temporal dentate gyrus to a point in which septotemporal differences are equalized. We finally show that intrinsic neuronal activity of developing DGCs is crucial for shaping the timing for maturation.
Neuronal activity modulates the timing of maturation of newborn DGCs
Voluntary locomotion was known to be coupled to neuronal activity in the hippocampus (Whishaw and Vanderwolf, 1973). In fact, the discharge rate of hippocampal pyramidal cells and interneurons was shown to increase with the running velocity even under conditions in which the animal was held in a fixed space but allowed to run (Czurkó et al., 1999; Maurer et al., 2005). In agreement, we observed that running increased the number of active neurons in the GCL. However, the fact that an increased proportion of active DGCs was only found in the temporal but not the septal dentate gyrus is surprising. Regional differences in the inhibitory network might contribute to the differential responsiveness to running. The number of inhibitory basket cells per DGCs is higher in the septal than the temporal dentate gyrus (Seress and Pokorny, 1981). In addition, CA1 pyramidal cells of both regions increased their firing rate as a function of running speed, whereas the spiking rate of CA1 interneurons was always higher in the septal region (Maurer et al., 2005).
However, previous studies have reported different levels of activity measured by Arc expression across the infrapyramidal and suprapyramidal blades of the rat granule cell layer after exploration or learning but not in caged controls (Chawla et al., 2005; Ramirez-Amaya et al., 2006; Snyder et al., 2009a). In agreement, we found no differences in the activity of the suprapyramidal vs infrapyramidal blades neither for the septal nor the temporal dentate gyrus in sedentary or running mice. Sedentary mice displayed significant differences in Arc expression for septal versus temporal areas (p < 0.0001) but not for suprapyramidal versus infrapyramidal blades (p = 0.19, two-way ANOVA; n = 9 mice). Interestingly, septotemporal differences on neuronal activity were equalized in running mice without differential effects on suprapyramidal versus infrapyramidal blades (p > 0.5 for both, two-way ANOVA; N = 9 mice). Therefore, both blades of the temporal dentate gyrus respond to voluntary movement in chronically running mice, in agreement with the higher involvement of the temporal hippocampus in sensorimotor processes (Bast and Feldon, 2003; Bast et al., 2009).
Interestingly, the rate of neuronal maturation correlated with the pattern of neuronal activity. Low levels of basal activity such as those seen in the temporal dentate gyrus of sedentary mice support a slow pace of development for newborn cells. In contrast, high network activity such as that found in the septal dentate gyrus of sedentary mice and in both septal and temporal areas of running mice promotes a higher rate of maturation. Finally, we found no differences in sedentary or running mice in the degree of maturation of neurons developing in different blades of the same dentate gyrus region as assessed by calbindin and DCX expression at 21 dpi (data not shown), supporting our conclusion that local network activity modulates neuronal development.
To investigate whether neuronal activity can directly modulate maturation, we analyzed the effect of decreased excitability by retroviral delivery of Kir2.1 into developing DGCs in running mice, the most active niche in our experimental conditions, in which basal activity and neuronal maturation in the septal and temporal dentate gyrus are equalized. Kir overexpression induced a significant reduction in the excitability of developing DGCs, yet neurons were not completely silenced. This moderate reduction in excitability induced a remarkable delay in maturation. Neurons expressing Kir exhibited prolonged expression of DCX and delayed onset of Cb when compared with control DGCs, and the dendritic tree and afferent connectivity remained diminished even after 35 d. It is noteworthy that newborn neurons mature over several weeks, yet little change was observed in mEPSC frequency and dendritic length in control DGCs between 21 and 35 dpi (Figs. 7E, 8A,B). This observation is consistent with our previous findings that the strength of excitatory connectivity increases abruptly at ∼3 and ∼6 weeks but remains unchanged within this time window (Mongiat et al., 2009). We speculate that neuronal connectivity might undergo extensive synaptogenesis and pruning during this interval (Shen and Scheiffele, 2010). Together, our results demonstrate that DGCs with reduced levels of intrinsic activity mature slower than those that are more active. This notion is consistent with the slower rate of maturation observed in the temporal dentate gyrus of sedentary mice. We conclude that the overall level of activity of the network determines the level of activity of each developing neuron and, consequently, controls the time during which newborn DGCs remain immature. We therefore propose activity-dependent modulation of neuronal maturation as a novel type of hippocampal plasticity.
Recent evidence has implicated electrical activity in the survival of adult-born neurons both in the hippocampus and olfactory bulb (OB). In the hippocampus, NMDA receptor activation promotes integration and survival of newborn DGCs (Bruel-Jungerman et al., 2006; Tashiro et al., 2006). In the OB, NMDA-mediated signaling is critical for neuroblast survival during migration along the rostral migratory stream (Platel et al., 2010). After migration has ended, intrinsic activity promotes the survival of neurons that are integrating in the OB circuitry (Lin et al., 2010). In addition, it was shown that altering the level of intrinsic activity did not affect the development of input or output connectivity in newborn cells of the OB (Kelsch et al., 2009). In contrast, our findings demonstrate that electrical activity greatly influences the rate of neuronal maturation and functional integration in the hippocampus.
Possible mechanisms underlying activity-dependent changes in neuronal maturation
In principle, the septotemporal differences in neuronal maturation might be determined in a cell-autonomous fashion, similarly to the distinct neuronal phenotypes arising from neural progenitor cells along the adult subventricular zone (Merkle et al., 2007). However, our observations highlight niche differences generated by the level of network activity as a primary modulatory mechanism that determines the rate of neuronal maturation. Our results demonstrate that the septal and temporal dentate gyrus display distinct activity set points that impinge on the rate of neuronal development. Changing those set points by running produced striking effects on maturation. Remarkably, those activity-dependent modifications occurred under physiological conditions.
Local network activity could modulate neuronal maturation by acting directly within developing neurons or by inducing secretion of factors from mature neighboring cells (Zweifel et al., 2005; Spitzer, 2006; Flavell and Greenberg, 2008). For instance, synthesis and secretion of neurotrophic factors such as brain-derived neurotrophic factor (BDNF), which participates in neuronal differentiation during adult neurogenesis, can be locally increased by electrical activity (Cotman and Berchtold, 2002; Bergami et al., 2008; Ma et al., 2009). In this work, we demonstrate that decreasing neuronal excitability by Kir overexpression reduces the rate of neuronal maturation, highlighting the crucial role of intrinsic activity in controlling this process. It is very likely that the effects of activity on maturation are triggered by subthreshold depolarization rather than by firing of action potentials. Consistent with this notion, we have previously shown that newborn DGCs begin to receive afferent excitation after ∼15 dpi, but they can only generate action potentials in response to an excitatory drive after 24–28 dpi (Mongiat et al., 2009). Intracellular effects of depolarizing activity might be mediated by the CREB signaling pathway, which has recently been involved in dendritic development and survival of adult-born DGCs (Jagasia et al., 2009). Therefore, BDNF and other released factors might act synergistically with intrinsic activity to shape neuronal maturation in the adult hippocampus, similarly to what has been described for BDNF actions on synaptic plasticity (Schinder and Poo, 2000).
Relevance of activity-dependent neuronal maturation in hippocampal function
The hippocampus is critical for episodic memory, forming unique memory traces about what, where, and when an event has occurred (Scoville and Milner, 1957; Ergorul and Eichenbaum, 2004). The dentate gyrus is the first processing stage of the hippocampus and it plays a critical role on the discrimination of similar visuospatial inputs, a necessary step for encoding episodic memory (Leutgeb et al., 2007). Adult neurogenesis in the dentate gyrus has been conserved through vertebrate evolution, and it may offer functional advantages because of the unique properties of young neurons (Treves et al., 2008). It was recently shown that developing DGCs display enhanced excitability and synaptic plasticity (Wang et al., 2000; Schmidt-Hieber et al., 2004; Ge et al., 2007; Mongiat et al., 2009). In addition, a relevant hypothesis on episodic memory formation has proposed that immature neurons would be activated by a broad range of stimuli because of their increased excitability, allowing association of temporally related events (Aimone et al., 2006). We propose two novel features to the current model that could modulate episodic memory encoding according to the animal's experience. First, the differential rate of neuronal maturation could provide different scales for encoding temporally related events in the septal and temporal dentate gyrus (Fig. 9). The shorter intervals of neuronal maturation in the septal region could be involved in highly detailed representations that demand a compressed timescale, whereas the prolonged window of maturation in the temporal region would provide an expanded scale for time associations of incoming inputs involving more generalized representations. Finally, network activity could shape these timescales of neuronal representation by modulating the timing for the expression of those unique functional properties acting at the level of neuronal maturation. Accelerating neuronal maturation could enhance temporal resolution and reliability on the encoding of multiple events by a high number of new neurons that are fast developing in the active network.
- Received March 18, 2011.
- Accepted April 5, 2011.
This work was supported by the Guggenheim Foundation Fellowship and by Agencia Nacional para la Promoción de Ciencia y Tecnología Grant PICT2005, the American Health Assistance Foundation (Alzheimer's Disease Research Grant A2007-078), the Delfina Baratelli Foundation, and the Howard Hughes Medical Institute (International Scholars Program Grant 55005963) (A.F.S.). A.F.S. and L.A.M. are investigators of the Argentine National Research Council [Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)]. V.C.P., M.G.D.-S., and M.S.E. were supported by doctoral fellowships from CONICET. We thank Mariela Veggetti for technical assistance, and Guillermo Lanuza, Antonia Marín Burgin, and Laura Ewell for critical suggestions and for comments on this manuscript.
The authors declare no competing financial interests.
- Correspondence should be addressed to Alejandro F. Schinder, Laboratory of Neuronal Plasticity, Leloir Institute, Consejo Nacional de Investigaciones Científicas y Técnicas, Avenida Patricias Argentinas 435, 1405 Buenos Aires, Argentina.
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