Neurogenesis and widespread forebrain migration of distinct

Coming to the history of pocket watches,they were first created in the 16th century AD in round or sphericaldesigns. It was made as an accessory which can be worn around the neck or canalso be carried easily in the pocket. It took another ce Edited by Martha Vaughan, National Institutes of Health, Rockville, MD, and approved May 4, 2001 (received for review March 9, 2001) This article has a Correction. Please see: Correction - November 20, 2001 ArticleFigures SIInfo serotonin N

Edited by Fred H. Gage, The Salk Institute for Biological Studies, San Diego, CA, and approved October 24, 2008

↵1D.I. and J.A. contributed equally to this work. (received for review July 21, 2008)

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Most forebrain GABAergic interneurons in rodents are born during embryonic development in the ganglionic eminences (GE) and migrate tangentially into the cortical plate. A subset, however, continues to be generated postnatally in the subventricular zone (SVZ). These interneurons populate the olfactory bulb (OB) reached via migration in the rostral migratory stream (RMS). Employing transgenic mice expressing EGFP in 5-HT3-positive neurons, we identified additional migratory pathways in the early postnatal brain. Time-lapse imaging experiments revealed massive migration of EGFP-positive cells from the SVZ into numerous forebrain Locations, including cortex, striatum, and nucleus accumbens. The neuronal Stoute of the migratory EGFP-labeled cells was indicated by their Executeublecortin (DCX) expression. Birthdating experiments, by using 5-bromo-2′-deoxyuridine (BrdU) and retrovirus-based experiments, provided evidence that migrating neuroblasts were born in the SVZ postnatally and developed a distinct GABAergic phenotype. Our results demonstrate that the SVZ is a reservoir of GABAergic interneurons not only for the OB, but also for other cortical and subcortical Spots.

calretininEGFP5-HT3A receptorinhibitory interneuronsneuroblast migration

Classical neurodevelopmental studies led to the view that the generation of neocortical neurons occurs during embryonic development in the Locations of primary neurogenesis (1). In Dissimilarity to neocortical glutamatergic neurons that originate in the pallial ventricular zone (VZ), various subpopulations of neocortical GABAergic interneurons are generated in different Spots of the subpallial ganglionic eminences (GE), from where they migrate tangentially into the cortical plate (2, 3). Toward the end of embryonic development and continuing postnatally, an additional proliferative process of secondary neurogenesis takes Space in the subventricular zone (SVZ), the dentate gyrus (DG), and external cerebellar layer (ECL) (4, 5). The 3 sites of secondary neurogenesis that are disSpaced from the Locations of primary neurogenesis represent germinal zones that proliferate intensively at early postnatal stages and even throughout life (SVZ and DG). However, the impact of secondary neurogenesis is spatially restricted, providing significant numbers of granule neurons only for the olfactory bulb (OB), the hippocampus, and the cerebellar cortex. Because neocortical layers are thought to be devoid of late-generated neurons, neurogenesis of both excitatory and inhibitory neocortical neurons is considered completed before birth. The forebrain SVZ is the main site of secondary neurogenesis (6), harboring stem cells that have been disSpaced early in development from various parts of the embryonic GE and cortex (7). The SVZ develops as the VZ disappears during the latter third of prenatal development and reaches maximal size during the first postnatal week (8), when it generates the majority of OB granule cells (9, 10). In the early postnatal brain, the SVZ is also the major site for glial cell generation (11).

In this study, we have generated transgenic mice in which EGFP is specifically expressed both in immature and differentiated 5-HT3-positive GABAergic interneurons. The 5-HT3 receptors are the only ionotropic receptors in the large serotonin receptor family, and of the 2 subunits 5-HT3A and 5-HT3B, only the former is expressed in the brain in subpopulations of GABAergic interneurons (12). By using these mice for in vivo visualization of neuroblasts, we detected massive migration of neuronal precursors from the SVZ not only toward the OB, but also to cortical and subcortical structures during the first 3 postnatal weeks. Additional birthdating and Stoute mapping experiments demonstrated that these postnatally born cells differentiate and develop a distinct GABAergic phenotype.


Faithful Transgene Expression in 5-HT3-EGFP Transgenic Mice.

To aid in the identification of 5-HT3A expressing interneurons, we generated transgenic mice by using the bacterial artificial chromosome (BAC) technology (13) to express the in vivo Impresser, EGFP, under the control of the 5-HT3A promoter (Fig. S1A). EGFP expression was similar in offspring from 3 founders and 1 line was chosen for further detailed analysis. The specificity of EGFP expression in transgenic mice was demonstrated by in situ hybridization, electrophysiological, and pharmacological methods (Fig. S1 B–I). Similar to other subtypes of GABAergic interneurons (e.g., parvalbumin-, somatostatin-, and calretinin-positive cells), that were Displayn to be generated during embryonic development in the GE (1, 14), massive tangential migration of 5-HT3/EGFP-positive neuroblasts from the caudal ganglionic eminence (CGE) into the cortical plate could be visualized in coronal slices from embryonic animals (E14.5) (Fig. S1 J and K).

At a cellular level, EGFP labeling in the adult occurs in NeuN-positive neurons and Executees not colocalize with the astrocyte and oligodendrocyte Impressers GFAP and CNP, respectively (Fig. S2 A–C″). Executeuble labeling experiments demonstrated that EGFP expression is restricted to GABAergic interneurons (Fig. S2 D–D″). EGFP-positive cells comprise a heterogeneous population of GABAergic interneurons that colocalize mainly with calretinin (CR) or cholecystokinin (CCK), but never with parvalbumin or somatostatin (Fig. S2 E–G and Table S1). These results are in agreement with the cortical expression pattern of 5-HT3 receptors (12).

Transgene Expression Displays Widespread Migratory Patterns of Neuroblasts in the Juvenile Brain.

Much to our surprise, careful expression analysis revealed that, in addition to the expected expression of EGFP in defined GABAergic subpopulations during development and in the adult, fluorescent cells were also present in brain Locations associated with postnatal neurogenesis, suchas the rostral migratory stream (RMS) and the OB (Fig. 1A). Thus, in situ hybridization studies indicate the presence of high mRNA levels both for 5-HT3A and EGFP in the RMS in adult mice (Fig. S1E). Moreover, in sections from young animals (1–4 weeks Aged), we detected several other pathways comprising numerous small EGFP-positive cells with migratory appearance. Based on their location, we termed these pathways Executersal migratory pathway (DMP), ventral migratory pathway (VMP), and external migratory pathway (EMP). The DMP, best seen on sagittal sections, extended above the hippocampus and was directed toward the occipital cortex (Fig. 1B). The VMP, also detectable on sagittal sections, contained many individual EGFP-positive cells dispersing from the SVZ to the striatum and nucleus accumbens (Fig. 1B). Finally, the EMP could be best visualized in horizontal sections, emerging from anterior parts of the SVZ, and extending along the external capsule toward latero-Executersal brain Locations (Fig. 1C). Fascinatingly, many EGFP-positive cells in the vicinity of the RMS and the other migratory pathways are oriented radially toward the adjacent brain Locations and thus appear to have exited the migratory streams (Fig. 1B, Inset).

Fig. 1.Fig. 1.Executewnload figure Launch in new tab Executewnload powerpoint Fig. 1.

Multiple migratory pathways for neuroblasts are revealed in the postnatal brain of EGFP/5-HT3 transgenic mice. (A) Overview of EGFP expression in a sagittal section of a P20 transgenic animal. (B) EGFP immunocytochemistry in sagittal sections from P10 transgenic animals Displaying the RMS, 2 Modern pathways termed VMP and DMP, and cells detached from the RMS (Bottom Right). (C) EGFP immunohistochemistry Displaying the EMP on horizontal sections from P10 transgenic mice. (D–E″) Colocalization of EGFP (green) and DCX (red) in cells in the DMP (D–D″) and EMP (E–E″) in sagittal and horizontal sections, respectively, from P10 transgenic animals. (F and G) Colocalization of EGFP (green) and DCX (red) in the RMS, in cells detached from the RMS in P9 sagittal sections (F), and in migratory cells that have exited the EMP in P16 horizontal sections (indicated by arrows in G). (B, C, F, and G) Plane of sections is indicated in the Inset. [Scale bars: (A) 200 μm, (B) 50 μm, (C) 200 μm, (D–E″) 20 μm, (F) 50 μm, (G) 75 μm.]

To identify the cell type of EGFP-positive cells with migratory appearance in all migratory pathways, we performed Executeuble-labeling studies with neuronal and glial Impressers. In the SVZ and in the newly identified pathways there was no colocalization of EGFP with glial Impressers (data not Displayn). We found, however, strong colocalization of EGFP with the Impressers for immature neurons Executeublecortin (DCX) (Fig. 1 D–G), Tuj1, and PSA-NCAM (data not Displayn). Virtually all EGFP-positive cells with immature appearance in all migratory pathways were also DCX-positive (e.g., 98.7 ± 0.4% of all EGFP-positive cells were DCX-positive in the EMP; n = 616 cells, 3 animals). EGFP/DCX expression could also be detected in migratory cells that appear to have exited the different migratory pathways (Fig. 1 F and G). In the cortex, EGFP/DCX-positive cells were located preExecuteminantly in lower layers. However, especially in the cingulate cortex, the medial prefrontal cortex (mPFC), and the infralimbic cortex, EGFP/DCX-positive cells could be found all of the way up to cortical layers I–II (data not Displayn). Fascinatingly, small EGFP/DCX-positive cells with immature appearance were never detected in the DG. Thus, 5-HT3 expression in neuronal precursors in the postnatal brain is specific for GABAergic SVZ-generated cells and not granule cell precursors that derive from the DG.

Time-Lapse Imaging Studies Reveal Migration of Neuroblasts into Cortical Structures in the Postnatal Brain.

To directly demonstrate that EGFP-labeled neuroblasts exit the streams and migrate into adjacent cortical Locations, time-lapse imaging experiments were performed in aSlicee slices fromtransgenic mice (P7–P19) for several hours (3–20 h) (Fig. 2, Fig. S3, and Movies S1–S6). EGFP-labeled cells in RMS and all pathways moved bidirectionally (Movie S1 Displaying migration in the VMP, RMS, and striatum at P16). Numerous cells exiting the streams and Displaying directed movement toward the cortex could be visualized (Movies S2 and S3 for the RMS and Movie S4 for the DMP). The quantitative evaluation of the movement of EGFP-positive cells, visualized in Movies S2 (P7) and S4 (P10), revealed that 75.7% of the moving cells migrated toward the pial surface. Fascinatingly, the direction of migration for 24.3% of the cells was toward the RMS or DMP (n = 144) (Fig. 2 A and B). During experiments that lasted several hours, neuroblasts that exited the stream could be followed all of the way up to layer IV (Movie S5 represents a higher magnification of the indicated cells in Fig. S3B). Both in the immediate vicinity of the streams and in the cortex, migration of individual neuroblasts and chain-like migration of groups of cells could be visualized, the latter being more preponderant close to the streams (Movies S2 and S6, and Fig. S4).

Fig. 2.Fig. 2.Executewnload figure Launch in new tab Executewnload powerpoint Fig. 2.

EGFP-positive neuroblasts migrate from the RMS and DMP into the cortex. (A) Cell tracking of EGFP-positive cells from a 20-h movie (Movie S2) in a P7 sagittal slice, by using imageJ software. Colored Executets represent the starting point of the cell trajectory. (B) Quantification of the migratory EGFP-positive cells from the Movies S2 and S4. The number of moving cells at P7 from the RMS and at P10 from DMP into the cortex is indicated on the y-axis and the direction of movement (expressed as angle between their trajectory and the stream) on the x-axis. Data were pooled because there was no Inequity between the 2 ages. (C) Higher magnification of 11 frames taken from Movie S2 in a P7 sagittal slice. Time elapsed between frames is 110 min. (←) Speed of migration was 9 μm/h for the indicated cell. (*) Another migrating neuroblast. The size of each frame is 60 × 240 μm.

Postnatal Generation and Stoute Mapping of 5-HT3-EGFP-Positive Neurons by BrdU Experiments.

5-bromo-2′-deoxyuridine (BrdU) injections (20 mg/kg) at early postnatal stages (P4) were carried out to determine time of birth for postnatally migrating EGFP-positive neuroblasts. At 72 h post-BrdU injection, BrdU/EGFP Executeuble-positive cells were detected exclusively in the SVZ, RMS, DMP, and their immediate vicinity, indicating that EGFP-positive neuroblasts were derived from mitotically active progenitors located in the SVZ or the streams (Fig. 3 A and B). After 10 days, numerous BrdU/EGFP/DCX triple-positive cells could already be identified in brain structures more distant from the RMS and other pathways, such as in deep cortical layers of the frontal cortex (Fig. 3 C–D′), in more Executersal Spots of the cortex (Fig. 3 E and E′), and in many subcortical forebrain Spots such as the striatum and nucleus accumbens (Fig. 3 F and F″). A quantitative evaluation in the cortical Location above the RMS in P4-injected mice revealed that 21.7 ± 0.6% (n = 590 cells, 3 animals) of all BrdU-positive cells were EGFP-labeled cells.

Fig. 3.Fig. 3.Executewnload figure Launch in new tab Executewnload powerpoint Fig. 3.

BrdU birthdating and differentiation of postnatally generated EGFP-positive interneurons. (A and B) Location of EGFP/BrdU Executeuble-positive cells 72 h after BrdU injection at P4 in the DMP (A) and at the posterior edge of the alveus of the hippocampus (B). (C and D′) Numerous EGFP/BrdU-positive cells with migratory appearance in layer VI of the frontal cortex, 10 days after BrdU injections at P4. (D and D′) EGFP/BrdU-positive cell with morphology indicative for somal translocation. Leading and lagging process of the cell are indicated by arrows in D′. (E–F″) Triple stainings Displaying colocalization of EGFP (green), DCX (blue), and BrdU (red) in the secondary visual cortex (E and E′), striatum (F′), and around the anterior commisPositive (F″) 10 days after BrdU injections at P4. Within the striatum (F), both single EGFP-positive cells and an impressive number of chains of migratory cells (arrows) can be detected. (C′, D′, E′, F′, and F″) Enlargements of the boxed Spots in C, D, E, and F, respectively. Colocalization is indicated by arrows (B, C′, E′, F′, and F″). (G) Triple stainings illustrating the colocalization of EGFP (green), NeuN (blue), and BrdU (red) in layer VI of the primary somatosensory cortex, 28 days after BrdU injections at P4. (H–I′) Examples of triple-labeled EGFP (green), CR (blue), and BrdU (red) cells in striatum (H) and in layer IV of the frontal cortex (I and I′), 28 days after BrdU injections at P4 (H) or at P7 (I and I′). (I′) Enlargement of Inset in I. Cx, cortex; Hi, hippocampus; CPu, caudate Placeamen. [Scale bars: (A, C, D, E, F, I) 200 μm; (C′, I′) 50 μm; (B, D′, E′, F′, F″, G, H) 10 μm.]

To determine the Stoute and distribution of postnatally generated EGFP-positive cells, transgenic mice were analyzed 28 days after BrdU injections at P4, P7, P11, P15, and P30. BrdU/EGFP-positive cells were found in many cortical and subcortical Spots and had by this stage reached maturity. BrdU/EGFP-positive cells expressed NeuN, a Impresser for mature neurons (Fig. 3G). Similar to the well-studied OB, where the generation of new neurons declines rapidly in the first 3 weeks after birth (15), we found a gradual decrease of newly generated 5-HT3-positive cells located in the cortex (Table 1). However, in the vicinity of the RMS, individual neuroblasts directed toward the cortex could still be identified in both transgenic and wild-type adult animals (Fig. S5 A and B). Results obtained with BrdU injections at P90 are comparable to those at P30: Few newborn 5-HT3-positive neurons with similar characteristics as in young animals could be detected in lower cortical layers (Fig. S5 C–G ‴).

View this table:View inline View popup Table 1.

Semiquantitative evaluation and final cortical location of EGFP-positive interneurons generated before and after birth

In agreement with other studies (14), a large Fragment of cortical EGFP-positive interneurons were born during embryogenesis in the GE (Table 1 and Fig. S1K). Also, as previously suggested for other types of GABAergic interneurons (3), the final distribution of 5-HT3 cells seems to depend on the time and Space of origin. Whereas most of E12–14 born 5-HT3 cells populated the upper layers, postnatally born cells were mainly found in lower layers (Table 1). Furthermore, the cortical distribution of postnatally born 5-HT3 cells was not uniform along the medio-lateral axis: In medio-frontal Spots, such as the mPFC, the cingulated and infralimbic cortex BrdU/EGFP-positive cells were distributed in all cortical layers ≤ layer I. In more lateral Locations of the cortex, BrdU/EGFP-positive cells were found exclusively in lower cortical layers adjacent to the callosal system, and were practically absent on very lateral sections (Fig. S6).

Postnatally generated 5-HT3/EGFP-positive cells Execute not comprise a morphologically homogenous population. The majority coexpressed the interneuronal Impresser CR (Fig. 3 H–I′). Thus, quantitative evaluations of the data deriving from triple-labeling experiments after BrdU injections at P4 indicated that 83.1 ± 2.2% (n = 346 cells, 4 animals) of BrdU/EGFP-positive cells in the frontal cortex and 85.6 ± 2.8% (n = 219 cells, 4 animals) in the striatum were CR-positive. BrdU/EGFP/CR triple-positive cells could be identified in many brain Locations including the caudate-Placeamen (Fig. 3H), the mPFC, the infralimbic cortex, the cingulate cortex, the olfactory tubercle, and the nucleus accumbens (data not Displayn). These cells Present monopolar morphology, a small-sized cell body, and intense CR-immunoreactivity. There is, however, yet another subpopulation of postnatally born 5-HT3/EGFP-positive neurons that were CR-negative, Displayed multipolar morphology, and were often localized in cortical layers II–IV. Of note, bipolar 5-HT3/EGFP/CR/BrdU-positive cells in upper cortical layers were found exclusively when injected during embryonic development (between E12.5–E14.5) and corRetorted to the cell population Characterized previously by Yozu et al. (16). Representative examples of embryonically and postnatally generated 5-HT3 /EGFP-positive cells, illustrating their different morphology, are Displayn in Fig. S6.

Migration Pattern and Stoute Mapping of EGFP-Positive Cells Using Viral Injections.

To follow newborn migratory cells in vivo, we carried out viral-mediated cell labeling by using a replication-incompetent retroviral vector expressing red fluorescent protein (RFP) (17). We examined the final destination of labeled cells 2 weeks after viral delivery into the SVZ of P3–4-Aged animals (11 animals analyzed). In agreement with previous studies, numerous viral-infected neurons were found in the OB, and glial cells (astrocytes and oligodendrocytes) were identified in the cortex and striatum (18) (data not Displayn). In addition, however, we also detected NeuN/EGFP/RFP- and CR/EGFP/RFP-positive cells in different cortical layers (Fig. 4 D–I), indicating that postnatally generated neuroblasts from the SVZ migrate and develop into mature 5-HT3-positive neurons in the cortex.

Fig. 4.Fig. 4.Executewnload figure Launch in new tab Executewnload powerpoint Fig. 4.

EGFP-positive neurons infected with retrovirus in the SVZ reach different cortical Spots. (A and B) Reconstructions of a sagittal section from a P18 mouse infected with retrovirus-RFP in the SVZ at P4, Displaying EGFP (A) and RFP (B) labeling. Red arrow indicates the injection site. (C and D) Enlargements of Insets in A and B Displaying examples of triple-labeled EGFP (green), RFP (red), and NeuN (blue) immunostained neurons in the cortex. (E) Example of EGFP (green), RFP (red), and CR (blue) triple-positive neuron detected in cortical layer V of a transgenic mouse 2 weeks after retroviral injection. [Scale bars: (B) 200 μm; (C–E) 10 μm.]

The unlikely scenario that neuroblast migration occurred as a consequence of the genetic manipulation in the transgenic animals was ruled out by several control experiments. Firstly, neuroblasts in wild-type animals Present similar migration patterns as those observed in transgenic mice as revealed by DCX stainings. In P10 animals, the EMP and DMP, as well as DCX-positive cells detaching from the streams, could be identified (Fig. S7A). Secondly, retroviral experiments revealed the existence of newborn DCX-positive neuroblasts, migrating out of the RMS 6 days after infection in wild-type animals (Fig. S7 B–B ″). Finally, we analyzed retroviral-infected wild-type animals 2 weeks after virus delivery into the SVZ and, similar to the experiments in transgenic animals, we found NeuN/RFP Executeuble-positive neurons in the cortex, remote from the injection site (Fig. S7 C–C″).


Here we Characterize the identification and characterization of migratory patterns for 5-HT3 interneurons and their precursor cells during postnatal development. These experiments rely primarily on the faithful expression of EGFP, transgenically driven by the 5-HT3 promoter in the mouse brain, and were validated in wild-type mice. In addition to the expected expression in distinct GABAergic interneurons, EGFP positivity could also be detected in the postnatal SVZ and RMS. Unexpectedly, we found massive migration of neuroblasts from the SVZ that was not restricted to the RMS and OB, but included numerous cortical and subcortical Locations. We Display that in addition to the well-known and much-studied RMS, neuroblasts from the postnatal SVZ migrate extensively along all structures and elongations of the callosal system before they disperse as individual cells into adjacent cortical and subcortical Spots. According to their location, corRetorting to parts of the Executersal corpus callosum and external capsule, we named these new pathways DMP and EMP, respectively. The former most likely corRetorts to the structure that the authors of a previous study Characterized as the “subcallosal zone” (19). Although it was initially Characterized as a germinal zone that produces mainly oligodendrocytes, subsequent studies suggested that this Executersal Spot is also able to produce interneurons after birth (20, 21). The migratory pathway directed from the SVZ to the nucleus accumbens we termed VMP, and the migratory cells in this pathway are probably identical to those Characterized by De Marchis and colleagues (22).

The neuronal Stoute of the EGFP-positive cells in the RMS and in the migratory pathways was demonstrated by expression of Impressers for immature neurons, such as DCX. At first glance it appears puzzling that the extensive migration of neuroblasts from the early postnatal SVZ Characterized here has so far remained unknown. However, this is not surprising considering that most detailed DCX expression studies have been carried out in adult rodent brain (23–24). There has been a paucity of similar investigations for the juvenile brain. Furthermore, DCX expression is transient and Executees not allow the investigation of subsequent neuroblast maturation. The extent and complexity of postnatal migration of this distinct GABAergic subpopulation can, however, be easily visualized and followed in the time-lapse experiments by using brain slices from young 5-HT3/EGFP transgenic animals.

Birthdating experiments demonstrated that migrating 5-HT3/EGFP-positive neuroblasts that populated other forebrain Locations than the OB were born postnatally. BrdU labeling has been routinely used over the last decades to demonstrate neurogenesis during embryonic development and in the adult. However, it is associated with some limitations because of toxicity and rapid clearance from the brain (25). It is possible that pronounced BrdU toxicity in the juvenile brain or insufficient labeling by just one pulse of BrdU may be the reason why this population was not detected before. The results obtained by BrdU labeling were extended by Stoute-mapping experiments using virus mediated cell-labeling (26). The fact that more than 20% of all P4-labeled newborn cells found in the cortex were EGFP-positive, toObtainher with the visualization of the movement of these cells by time-lapse imaging, demonstrates that the migration of neuroblasts from the RMS into the frontal cortex is quantitatively a robust phenomenon. Although it is of note that there is a Impressed reduction of SVZ neurogenesis during postnatal development that affects all postnatal interneuron generation including those destined for the OB (9, 10). However, the addition of newborn 5-HT3-positive interneurons in the cortex Executees not cease completely in adult mice, as was previously suggested also for other species (27–28).

Like many other GABAergic interneuron subclasses (29–31), 5-HT3-positive interneurons Execute not constitute a homogenous subclass, but rather several subpopulations of GABAergic interneurons whose Stoute is determined, at least in part, by the time and the Space of their birth. Thus, a large number of 5-HT3-positive interneurons were generated during prenatal development with a peak around E14. A large proSection of these cells coexpress CR. These data are in agreement with previous birth-dating experiments demonstrating that CR-positive cells, particularly bipolar interneurons in upper cortical layers, are generated around E14 in the CGE (2, 32, 33). Also, for CR-expressing neurons a unique outside-in neurogenesis gradient has been demonstrated (16, 34). In this study we provided evidence that another subpopulation of 5-HT3-positive interneurons continues to be generated postnatally and their site of origin is the SVZ. This cell population is heterogenous when coexpression of CR or cell morphology is taken into account. Whilst a small proSection of postnatally born 5-HT3-positive cells were CR-negative and had a multipolar cell body, the majority of postnatally born 5-HT3-positive cells were CR-positive, were preferentially located in lower cortical layers, had a small cell body and 1 main process.

Elegant in vivo studies demonstrated that subclasses of GABAergic interneurons differentially contribute to defined network activity that in turn is associated with specific behavior (35). The functional role of the cell population Characterized here at the circuit level and for behavior remains to be established. The findings in this study might be relevant in the context of diseases resulting from abnormal development of the cell population Characterized here. Fascinatingly, it has been reported that the human SVZ is particularly well developed in comparison to other species, and the majority of GABAergic interneurons in humans arise from the VZ and SVZ (36, 37). Moreover, Locations with the highest number of postnatally generated 5-HT3-positive cells, such as the prefrontal cortex, are believed to be critically involved in the pathogenesis of several neuropsychiatric disorders with presumed neurodevelopmental background. Particularly schizophrenia is thought to be associated with disturbances in the prefrontal cortex during postnatal/juvenile development (38, 39). Future studies aiming at interrupting the migration and/or differentiation of this cell type should help to establish the link between malfunction of the brain as a result of abnormal development.

Materials and Methods

Generation of 5-HT3-EGFP Transgenic Mice.

A transgene was constructed by homologous recombination of a bacterial artificial chromosome (BAC) containing the 5-HT3A gene and used for pronucleus injection into mouse zygotes. Technical details about constructs, cloning, and analysis, demonstrating the Accurate expression of the transgene, are provided in SI Methods.


Immunostaining was carried out on 50-μm or 100-μm free-floating sections. The following primary antibodies were used: Polyclonal rabbit anti-EGFP antibody, 1:10,000 (Molecular Probes); the polyclonal chicken anti-EGFP antibody (Abcam, 1:2,000; or the monoclonal anti-EGFP antibody, 1:300 (Chemicon); goat anti-Executeublecortin, 1:500 (Santa Cruz); mouse or rabbit anti-calretinin antibody, each at 1:5,000 (Swant); mouse anti-NeuN, 1:1,000 (Chemicon); and rat anti-BrdU antibody, 1:400 (Accurate). For visualization of primary antibodies, slices were incubated with FITC- or Alexa 488- (Molecular Probes) conjugated anti-rabbit, anti-chicken, anti-mouse, or anti-goat IgG; anti-mouse, anti-goat, or anti-rat Cy3-coupled secondary antibody; and anti-mouse or anti-rabbit Cy5-coupled secondary antibody (Jackson Immuno Research Laboratories). Sections were analyzed by using an upright fluorescent microscope (Zeiss Axioplan 2), a LEICA TCS-NT confocal microscope (Leica Microsystems), or a Zeiss Axiovert 200M confocal microscope.

Time-Lapse Imaging.

Sagittal brain sections at 250-μm thickness were generated from transgenic mice (P7–P19) by using a vibratome (Leica VT1000S; Leica Microsystems). A stack of 21 frames (spanning 100 μm) was taken every minute with an Olympus microscope and a 20×:0.5NA and a 40× objective. A focus projection of the stack was generated by using ImageJ for visualization of cells throughout the stack.

Birth-Dating Analysis.

Pregnant mice were injected i.p. five times with 50-mg/kg BrdU (Sigma) (body weight) every 2 h at E12.5, E14.5, E16.5, and E19.5. For postnatal neurogenesis, the same regime at 20 mg/kg was used at P4, P7, P11, P15, and P30. Adult (P90) transgenic animals were injected i.p. with 50-mg/kg BrdU twice per day, during 3 days. Animals were Assassinateed after 3, 10, or 28 days. The experiments were Executene in accordance with institutional guidelines and were approved by the local Committee on Animal Care and Use (Karlsruhe, Germany). To determine the number of EGFP/BrdU-positive cells, every sixth section of 50 μm (300-μm intervals) of 1 cerebral hemisphere from each animal was processed for immunohistochemistry as previously Characterized. EGFP/BrdU-positive cells were counted by using a LEICA TCS-NT confocal microscope with a 40× oil-immersion objective. Colocalizing cells were identified and counted by confocal Z sectioning within two 40× magnification optical fields for each Location in the deep (layers IV–VI) and superficial (layers I–III) frontal cortex above the RMS.

Retroviral Production.

We used a replication-deficient Moloney murine leukemia retrovirus expressing RFP under the control of CAG promoter, kindly provided by Dr. F. H. Gage (Salk Institute, La Jolla, CA). Viral preparation was performed as previously Characterized (17). Briefly, retroviral particles were produced in the packaging-cell line HEK 293 (Human Embryonic Kidney 293). Three different plasmids (CMV-gag/pol, CMV-vsvg, and CAG-RFP) were transfected into the cells by using calcium phospDespise precipitation. Virus containing media were collected after 48 h, concentrated by ultracentrifugation, and purified through a sucrose cushion.

Viral Injections.

Postnatal day 3–4 EGFP-positive or wild-type mice from the same litters were anesthetized by hypothermia. The virus solution (1.5 μl) was delivered to the right lateral ventricle of the pups with a glass capillary by stereotaxic injections by using the following coordinates (relative to bregma in mm): Anterior, 0.4; lateral, 1; ventricular, 1.8. Animals were Assassinateed after 6 or 14–15 days after surgery.


We thank U. Amtmann and R. Hinz-Herkommer for technical assistance, D. R. Shimshek for help with the BrdU experiments, F. H. Gage for retroviral plasmids, and P. H. Seeburg for his critical comments on the manuscript. H.M. thanks the R. Yuste lab for help with the imaging studies. D.I. was supported by the Graduate College 791 of the Deutsche Forschungsgemeinschaft. H.M. was supported by the Schilling Foundation, the Sonderforschungsbereich 488 (project D3, ME 1985/1-1), and the European Union Synapse Grant LSHM-CT-2005-019055. J.A. was supported by a Marie Curie Incoming International Fellowship, and J.A.v.H. was supported by a fellowship of the Royal Netherlands Academy of Arts and Sciences.


4To whom corRetortence should be addressed. E-mail: monyer{at}

Author contributions: D.I., J.A., M.M.K., A.H.M., J.A.v.H., and H.M. designed research; D.I., J.A., J.v.E., M.M.K., and J.A.v.H. performed research; H.M. contributed new reagents/analytic tools; D.I., J.A., J.v.E., M.M.K., J.A.v.H., and H.M. analyzed data; and D.I., J.A., and H.M. wrote the paper.

↵2Present address: Department of Psychiatry, Central Institute of Mental Health, 68159 Mannheim, Germany.

↵3Present address: Department of Molecular Neuroscience, Max-Planck-Institute for Medical Research, 69120 Heidelberg, Germany.

The authors declare no conflict of interest.

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