Programmed cell death in type II neuroblast lineages is required for central complex development in the Drosophila brain
© Jiang and Reichert; licensee BioMed Central Ltd. 2012
Received: 9 September 2011
Accepted: 18 January 2012
Published: 18 January 2012
The number of neurons generated by neural stem cells is dependent upon the regulation of cell proliferation and by programmed cell death. Recently, novel neural stem cells that amplify neural proliferation through intermediate neural progenitors, called type II neuroblasts, have been discovered, which are active during brain development in Drosophila. We investigated programmed cell death in the dorsomedial (DM) amplifying type II lineages that contribute neurons to the development of the central complex in Drosophila, using clonal mosaic analysis with a repressible cell marker (MARCM) and lineage-tracing techniques.
A significant number of the adult-specific neurons generated in these DM lineages were eliminated by programmed cell death. Programmed cell death occurred during both larval and pupal stages. During larval development, approximately one-quarter of the neuronal (but not glial) cells in the lineages were eliminated by apoptosis before the formation of synaptic connectivity during pupal stages. Lineage-tracing experiments documented the extensive contribution of intermediate neural progenitor-containing DM lineages to all of the major modular substructures of the adult central complex. Moreover, blockage of apoptotic cell death specifically in these lineages led to prominent innervation defects of DM-derived neural progeny in the major neuropile substructures of the adult central complex.
Our findings indicate that significant neural overproliferation occurs normally in type II DM lineage development, and that elimination of excess neurons in these lineages through programmed cell death is required for the formation of correct neuropile innervation in the developing central complex. Thus, amplification of neuronal proliferation through intermediate progenitors and reduction of neuronal number through programmed cell death operate in concert in type II neural stem-cell lineages during brain development.
The Drosophila central brain is a highly complex neural structure comprising several tens of thousands of neural cells that are organized into the intricate synaptic circuitry of the neuropile. The neurons of the brain are generated during development by a remarkably small set of approximately 100 bilaterally symmetrical pairs of neural stem-cell-like primary progenitors referred to as 'neuroblasts' [1, 2]. These neuroblasts undergo two phases of neurogenesis; the first takes place during embryogenesis, and the second occurs during the post-embryonic larval phase [3, 4]. During embryonic neurogenesis, the brain neuroblasts produce the primary neurons of the larval brain. After a quiescent phase, most of the same neuroblasts restart their proliferative activity, and produce the adult-specific secondary neurons of the adult brain during larval development. These secondary neurons, which represent approximately 95% of the neurons present in the adult brain, form synaptic interconnections during subsequent pupal development.
Recent work has shown that the neuroblasts of the brain can be divided into two classes: type I and type II. Most of the neuroblasts in the fly brain are type I neuroblasts, which generate their neural progeny via a non-self-renewing intermediate progenitor called a ganglion mother cell (GMC), which divides only once to give rise to two post-mitotic cells, either neurons or glial cells [5–8]. By contrast, eight identified type II brain neuroblast pairs generate their progeny through self-renewing intermediate neural progenitors (INPs), which have features of transit amplifying cells. Because an INP undergoes several rounds of proliferative cell divisions, each of which results in self-renewal of the INP and in the generation of a GMC that produces two neural progeny, a marked amplification of proliferation occurs in type II lineages [9–11]. Thus, whereas most type I neuroblasts generate neural lineages consisting of approximately 100 to 150 adult-specific neurons, type II neuroblasts typically give rise to adult-specific neural lineages that are 3 to 5 times larger (range 370 to 580 ).
Recent studies have indicated that the amplifying type II neuroblast lineages primarily contribute neural cells to a complex unpaired neuropile center in the adult brain, called the central complex [12–14]. The central complex is located in the midline of the protocerebrum, and comprises several thousand neurons, corresponding to approximately 50 cell types that project into several major modular compartments, including the ellipsoid body (EB), fan-shaped body (FB), noduli (NO), and protocerebral bridge (PB), as well as associated accessory regions. A comprehensive neuroblast lineage-based analysis indicates that most of the adult-specific neurons in the central complex derive from 10 identified neuroblast lineages . Prominent among these are the type II neuroblast lineages, notably the six type II lineages located at the posterior dorsomedial edge of the brain hemispheres termed DM1 to DM6 [9, 12]. For example, four of these DM lineages (DM1 to DM4) generate the central complex small-field neurons that link the major neuropile modules of the central complex [12, 15]. Thus, a relatively small number of amplifying type II neuroblasts generates a remarkably large number of adult-specific central complex neurons during a relatively short period of post-embryonic development.
Although the amplification of neural stem-cell proliferation through INPs can generate large numbers of progeny in a short time, it is sensitive to dysregulation, which can result in overproliferation and tumorigenesis. Thus, tight control of proliferation in both the neuroblast and the INP is essential to prevent this type of dysregulation . In addition to this restriction of the developmental potential of progenitors, programmed cell death also plays an important role in regulating both the number of proliferating progenitors and the number of their post-mitotic neural progeny. Prominent programmed cell death of type I neuroblasts and neurons has been documented in the brain and ventral nerve cord during embryonic and post-embryonic neurogenesis [17–23]. Moreover, lineage-specific programmed cell death has recently been reported in post-embryonic development of the Engrailed-expressing neuronal lineages in the brain, and in identified neuroblast lineages in which cell death is limited in specific hemilineages [24–26]. However, nothing is currently known about a potential role for programmed cell death in the amplifying type II neuroblast lineages. Given the large number of neurons produced in these lineages and their susceptibility to overproliferation, programmed cell death could play an important regulatory role in their development.
In this study, we used clonal mosaic analysis with a repressible cell marker (MARCM)  and lineage-tracing techniques to investigate programmed cell death in the amplifying DM lineages that contribute neurons to central complex development. We found that programmed cell death occurred in the amplifying DM lineages during both larval and pupal stages. During larval development, approximately one-quarter of the neuronal (but not glial) cells in the lineages were eliminated by apoptosis before the formation of synaptic connectivity during pupal stages. Lineage-tracing experiments document the extensive contribution of INP-containing DM lineages to all of the major modular neuropile substructures of the adult central complex. Moreover, blockage of apoptotic cell death specifically in these lineages led to prominent innervation defects of DM-derived neural progeny in all the major substructures of the adult central complex neuropile. Our findings indicate that significant neural overproliferation normally occurs in DM lineage development, and that elimination of excess neurons in these lineages through programmed cell death is required for the formation of correct neuropile innervation in the developing central complex.
Programmed cell death occurs in DM lineages during post-embryonic development
Six of the eight type II neuroblasts present in each half of the central brain are located at the posterior dorsomedial edge of the hemisphere. These six neuroblasts and their respective lineages have been referred to as DM1 to DM6 by Bello et al. , and they tentatively correspond to the DPMm1 (DM1), DPMpm1 (DM2), DPMpm2 (DM3), CM4 (DM4), CM3 (DM5), and CM1 (DM6) lineages neuroanatomically defined by Pereanu et al. . A large number of neurons in these DM lineages makes major contributions to the central complex [12, 13, 15]. Because they are relatively easy to identify, most investigations of type II neuroblast lineages have focused on DM1 to DM6.
To determine if some of the neurons generated in these DM1 to DM6 lineages might be eliminated by lineage-specific programmed cell death, we combined a lineage-tracing method with targeted apoptosis block. For DM-specific lineage tracing, we used the erm-Gal4 R09D11 driver together with UAS-flp actin>CD2>Gal4, resulting in FLP-out clones that permanently expressed GAL4 in all of the neural progeny of all DM lineages . In the larval central brain, the erm-Gal4 R09D11 driver alone specifically targets all mature INPs and their young progeny; however, it does not target all of these neural progeny in pupal stages or in the adult, thus making this type of lineage tracing necessary [13, 28–30]. A DM-specific apoptosis block was attained by combination of this erm-Gal4 R09D11 -based lineage-tracing method with UAS-p35; the latter expresses the baculovirus anti-apoptotic protein P35 . DM-specific labeling was attained by UAS-mCD8::GFP, and general synaptic neuropile labeling by the widely used nc82 monoclonal antibody [32–34].
Identification and quantification of apoptotic cells in DM lineages during larval development
The overall organizational features of the wild-type DM1 lineage were documented in single optical sections of the MARCM labeled clones. A single large cell corresponding to the DM1 neuroblast was associated with a large cluster of labeled neural progeny (Figure 3D, arrowhead). Axons from these neural progeny fasciculated to form a secondary axon tract (SAT), which started within the cluster of labeled cells (Figure 3E, arrow). The overall extent of the labeled clone, shown by a superimposition of all single optical sections containing labeled cells, had the typical size and position of the wild-type DM1 lineage as reported by previous studies (Figure 3F) [12, 30]. When corresponding single sections were documented for cell-death-blocked DM1 mutant clones, marked increases in the number of labeled cells were seen. This was especially evident in single optical sections taken at the level of the mutant DM1 neuroblast (Figure 3G, arrowhead; compare with Figure 3D). However, an increase in the number of labeled cells in mutant clones was also apparent in single sections taken at the level of the SAT (Figure 3H, arrow; compare with Figure 3E). Correspondingly, superimposition of all optical sections containing labeled cells showed a marked increase in size and cell number in the labeled apoptosis-blocked mutant DM1 clone (Figure 3I; compare with Figure 3F). The thickness of the SAT was increased in the apoptosis-blocked mutant MARCM clone, whereas the projection pattern of the SAT at the end the late third larval instar was the same as that seen in wild-type MARCM clones, and no ectopic axon projections were formed in the larval brain ([12, 30]; data not shown).
To quantify the increase in cell number, we counted the number of labeled cells in a series of wild-type versus apoptosis-blocked mutant DM1 neuroblast clones (Figure 3B). Wild-type DM1 clones (n = 6) had an average of 367 ± 51 labeled cells, whereas the apoptosis-blocked mutant DM1 clones (n = 11) had an average of 500 ± 49 labeled cells. These findings indicate that 27% of the cells generated in DM1 clones are eliminated by apoptosis during larval development. To determine if the affected cells in the DM1 lineage were neurons or glial cells, we labeled wild-type and apoptosis-blocked mutant neuroblast clones with the glia-specific anti-Repo antibody, which reliably recognizes the glial cells in DM clones . Counts of the number of the Repo-labeled cells did not reveal a difference in glial cell number in wild-type DM1 clones (16 ± 0.8; n = 4) versus mutant DM1 clones (16 ± 0.9; n = 7) (Figure 3C), indicating that the cells affected by apoptosis in DM1 lineages were neuronal but not glial cells. We conclude that programmed cell death eliminates approximately one-quarter of the neurons generated in the DM1 lineage during larval development.
Cell number in wild-type and apoptosis-blocked intermediate neural progenitor clones (e.g. H99)
Wild-type (n = 4)
5.3 ± 0.5
2.5 ± 0.6
2.8 ± 0.5
H99 (n = 4)
9 ± 0.8
6.5 ± 0.6
2.5 ± 0.6
Although additional programmed cell death occurs during pupal development (Figure 2), we were not able to reliably identify DM1 neuroblast clones in the pupal stages because the lineage-related neurons changed position and no longer formed compact groups during metamorphosis . Consequently, we could not accurately determine the number of cells that underwent programmed cell death in the DM1 lineage during pupal development.
Blocking programmed cell death results in central complex neuropile innervation defects of DM lineage neurons
Our findings indicate that a significant level of programmed cell death occurs in the neural cells of DM lineages during normal development. To investigate the role of the normally occurring programmed cell death, we used lineage tracing to assay the contribution of wild-type DM lineages versus apoptosis-blocked DM lineages to the major neuropile compartments of the central complex in the adult brain. In these experiments, we combined synaptic neuropile labeling using the nc82 antibody with DM neuron-specific labeling using the erm-Gal4 R09D11 lineage-tracing method (see above).
The neuropile of the FB is located posterior to the ellipsoid body and represents the largest central complex compartment of the Drosophila brain. In the wild-type brain it is subdivided into several regularly vertical and horizontal strata (Figure 4E, G). Labeling of the neuropile innervation from wild-type DM lineages identified a major contribution to the FB neuropile, as virtually all strata, either horizontal or vertical, received ordered innervation (Figure 4F, H). When apoptosis was blocked in DM lineages, the overall organization of the FB compartment as shown by nc82 labeling appeared normal, but some regions within the compartment appeared to lack synaptic neuropile (Figure 5E, G). Specific labeling of the neuronal innervation from the apoptosis-blocked DM lineages was clearly abnormal (Figure 5F, H), with lack of innervation in some strata (Figure 5H, arrowheads) and aberrant concentration of arborizations in others (Figure 5H, arrows). As in the case of the EB, this type of perturbed innervation in the FB contrasted with the relatively uniform innervation seen in wild-type DM lineages (Figure 4H).
The neuropile of the two bilaterally symmetrical NO is located ventrally to the FB, and is composed of three distinct and regularly arranged layers, as shown in the nc82-labeled wild-type brain (Figure 4I, K). The NO showed innervation from the wild-type DM lineages in all three layers (Figure 4J, L). In brains with apoptosis-blocked DM lineages, although NO were present, they were often misarranged (Figure 5I, K). Thus, nc82 labeling identified deformation in size and position of the three-layered structure of the neuropile (Figure 5K, arrow). Labeling of innervation from the apoptosis-blocked DM lineages reflected (and was probably the cause of) this dramatic misarrangement (Figure 5J, L). For instance, the bilaterally symmetrical organization of the three layers was lost in these brains (Figure 5L, arrow).
The neuropile of the m-shaped PB is located in the most posterior position relative to other central complex compartments (Figure 4M, O). It is divided into 16 segmental units, but these are revealed only poorly by nc82 labeling in wild-type brain. The two halves of the PB neuropile were innervated in a regular manner by lineage-specific labeled processes from the wild-type DM lineages, but this labeling was somewhat obscured because of the proximity of labeled cell bodies of the neurons projecting to the protocerebral bridge (Figure 4N, P). In brains with apoptosis-blocked DM lineages, the PB was present, but perturbations in the nc82 labeled neuropile of the protocerebral bridge were evident as breaks or deletions (Figure 5M, O, arrow). These breaks and deletions in PB innervation appeared to be amplified in specific labeling of projections from the apoptosis-blocked DM lineages (Figure 5N, P, arrow). Taken together, these findings indicate that abnormal innervation of major compartments of the central complex occurs specifically for the neurons from apoptosis-blocked DM lineages. In approximately one-third of the mutant flies, apoptosis blockage of DM lineages resulted in abnormal innervation of all four major central complex neuropile compartments, and in another third of the mutant flies, three of the four major central complex compartments had abnormal innervation (see Additional file 2, Table 1). We conclude that the extensive programmed cell death of neurons that occurs in DM lineages is essential for correct innervation of the central complex neuropile by these lineages.
In contrast to the abnormal innervation of neuropile compartments by arborizations of neurons from apoptosis-blocked DM lineages, the axonal projections of these neuronal lineages from their cell body clusters to the adult central complex neuropile were normal (data not shown). Moreover, all mutant flies were viable and fertile, and no obvious behavioral consequences of apoptosis blockage in DM lineages were seen; mutant flies had normal walking and climbing behavior in simple negative geotaxis and positive phototaxis assays.
Development of central complex innervation defects in apoptosis-blocked DM lineage neurons
During the first two days of pupal development, the primordium of the central complex compartments becomes recognizable, undergoes characteristic shape changes, and grows in size as a result of the lineages that innervate the central complex form terminal arbors in the neuropile during this time . To investigate the role of the normally occurring programmed cell death during this process, we used lineage tracing to characterize the projections of wild-type DM lineages versus apoptosis-blocked DM lineages to the primordium of the central complex in the pupal brain.
At 48 hours APF, the wild-type central complex primordium was already comparable with that of the mature adult structure (Figure 6I, K). The primordium of the EB had closed to form its characteristic ring-shaped appearance (Figure 6I), the FB primordium had the characteristic size and shape of the adult structure (Figure 6K), and the primordia of the NO formed a bilaterally symmetrical multilayered neuropile flanking the midline (Figure 6K). Labeled neuropile processes from wild-type DM lineages innervated all of these primordia in a regular manner, and this innervation often revealed subcompartments such as in the EB primordium (Figure 6J, L). The general arrangement of the central complex primordium at 48 h APF in pupal brains with apoptosis-blocked DM lineages was comparable with that of wild-type brains, and the primordia of all central complex subcompartments were evident (Figure 6M, O). However, the labeled neuropile processes from apoptosis-blocked DM lineages showed clear signs of abnormal innervation in these primordia (Figure 6N, P). For example, labeled processes in the EB were seen to aggregate strongly in some parts of the ring-shaped compartment (Figure 6N, arrows) and the FB primordium (Figure 6P, arrowheads), and misarrangement of the layers of the NO neuropile was also seen in these brains (Figure 6P, arrow).
We conclude that initial signs of abnormal innervation from apoptosis-blocked DM lineages are visible in the developing central complex primordium at 24 hours APF, and that prominent abnormal innervation by these apoptosis-blocked lineages becomes apparent at 48 hours APF. We posit that the initial defects in innervation in the early pupal brain form the basis for the severe abnormal innervation that characterizes apoptosis-blocked DM lineages in the adult central complex.
In this study, we used a combination of genetic lineage tracing, clonal MARCM techniques, and molecular labeling to study programmed cell death in the DM type II neuroblast lineages that make major contributions to the central complex neuropile. Our data indicate that extensive programmed cell death occurs in these lineages during post-embryonic development, and that this lineage-specific cell death is important for the establishment of appropriate innervation of the DM lineage-derived neurons in the adult central complex. These findings have implications for understanding the mechanisms that underlie type II neuroblast proliferation, post-embryonic neural development, and the formation of complex circuitry in the central brain.
Programmed cell death has been widely studied in development of the central nervous system of Drosophila. Most of these studies have focused on lineages in the developing ventral nerve cord, in which cell death controls neuroblast and neural cell survival, often in a segment-specific manner [18–22, 26, 39, 40]. Recently, lineage-specific programmed cell death has been reported in central brain development, and related to specific sublineages. A study of the four Engrailed-expressing neuroblast lineages in the brain shows that apoptosis specifically affects the Engrailed-negative cells in two lineages and the Engrailed-positive cells in another lineage in a process that is regulated by Notch signaling . A comparable study of three identified neuroblast lineages that innervate the antennal lobe indicates that programmed cell death can target individual hemilineages in a Notch/Numb-dependent manner . However, all of these investigations have been carried out on type I neuroblast lineages, and nothing was known about the existence of programmed cell death in the novel type II neuroblast lineages that amplify proliferation through INPs.
The experiments reported here indicate that programmed cell death plays a prominent role in the development of type II lineages. This means that the same single neuroblast lineage initially amplifies the number of neuronal cells through transit amplifying cell-like INPs, and subsequently reduces the number of neuronal cells that survive through apoptosis. This suggests that programmed cell death in these lineages may contribute to the balance between self-renewal and differentiation, which might otherwise contribute to depletion or overproliferation in these lineages [7, 8]. Notably, uncontrolled overproliferation in these amplifying neuroblast lineages can lead to dramatic defects. For example, dramatic overgrowth and tumor formation in the developing Drosophila brain can occur if any one of several key cell-fate determinants that are normally segregated from the type II neuroblasts to their INP daughter cells to ensure differentiation are perturbed [16, 41, 42]. Interestingly, approximately one-quarter of the adult-specific neurons in the DM lineages that are targeted by apoptosis are both generated and eliminated during larval development before their parent DM neuroblasts cease their proliferative activity. Because adult-specific neurons only differentiate fully to form functional interconnections during subsequent pupal development, the affected cells are probably eliminated before they form synapses and integrate into the functional circuitry. However, apoptosis in these lineages is not limited to larval stages; it also occurs during early pupal stages when adult-specific DM neurons arborize and form synaptic connections that give rise to mature neuropile structures such as the central complex. It will be important to investigate this pupal phase of DM neuron apoptosis further, because it may indicate that neurons that fail to form appropriate synaptic interconnections in the neuropile are targeted by programmed cell death.
Our findings indicate that programmed cell death in DM lineages plays an important role in determining the innervation of the DM-derived neurons in the central complex neuropile. In the absence of apoptosis, aberrant and often asymmetric arborizations from these neurons are formed in all of the major substructures of the central complex neuropile. Moreover, these innervation defects are often accompanied by prominent neuropile disruptions, such as malformation of the NO or breakage in the PB. Our data document the major contribution of DM lineage-derived neurons to the developing central complex, and confirm similar findings by previous authors [12, 13, 30]. It is likely that comparable lineages contribute to central complex formation in other insects. Recent work in the grasshopper Schistocerca gregaria showed that four identified neuroblasts that are similar to DM1 to DM4 in Drosophila in terms of location and type of proliferation, also generate the numerous small-field neurons of the central complex [43, 44]. Moreover, the lineages that are generated by these four grasshopper neuroblasts are targeted by programmed cell death, resulting in approximately 20% of the neurons being eliminated during embryonic development . These remarkable similarities in a holometabolic insect such as Drosophila and a hemimetabolic insect such as the grasshopper, which are separated by at least 300 million years of evolution, imply that comparable neuroblasts, neuronal proliferation modes, and lineage-specific programmed cell death operate in the development of the central complex in most, if not all, insects .
The insect central complex is an intricate, high-level, multimodal information- storage and -processing center that is involved in motor coordination of behaviors such as walking, flying and stridulation . In neuroanatomical terms, it represents a highly complex midline neuropile made up of several thousands of neurons, corresponding to approximately 50 cell types that are arranged in a highly ordered architecture. Remarkably, the large number of neurons that contribute to the central complex is generated by a small number of neuroblasts during a short developmental time period. Indeed, the amplification of DM neuroblast proliferation through INPs, which act as transient amplifying cells, may be an important mechanistic prerequisite for rapidly generating the large number of neurons required for complex central circuitry. Comparable amplification of neural stem-cell proliferation through transit amplifying cells is present in the developing brains of vertebrates including mammals. Notably, in mammalian cortical development, the wealth of neurons required for complex circuitry is largely generated by neural stem cells via INP-like progenitor cells called basal progenitors [46–48]. Given that this type of amplification of neural proliferation may be a general strategy for increasing the size and complexity of the brain, a concurrent and potentially counter-balancing role of programmed cell death in neural stem-cell lineages may also be a general and evolutionarily conserved mechanism for generating brain complexity.
♦ y w hs-flp; tub-Gal4 UAS-mCD8::GFP LL5 /CyO act-GFP JMR1 ; FRT2A tub-Gal80 LL9
♦ w; FRT2A
♦ w; FRT2A H99 kni ri -2/TM6B
♦ w; UAS-mCD8::GFP LL5 ; erm-Gal4 R09D11
♦ y w UAS-flp; If/CyO y + ; act>CD2>Gal4 erm-Gal4 R09D11 UAS-mCD8::GFP LL6 /TM6B
♦ w; UAS-p35; erm-Gal4 R09D11 UAS-mCD8::GFP LL6
To generate wild-type MARCM clones, virgin females of y w hs-flp; tub-Gal4 UAS-mCD8::GFP LL5 /CyO act-GFP JMR1 ; FRT2A tub-Gal80 LL9 were crossed with w; FRT2A males. Homozygous H99 MARCM clones were generated by crossing virgin females of y w hs-flp; tub-Gal4 UAS-mCD8::GFP LL5 /CyO act-GFP JMR1 ; FRT2A tub-Gal80 LL9 with w; FRT2A H99 kni ri -2/TM6B males. Embryos from the above crosses were collected on agar plates for 4 hours and raised at 25°C for 22 hours before undergoing heat-shock treatment. Heat-shock induction of Flippase was performed by immersing the agar plates in a water bath at 37°C for 60 minutes (for neuroblast clones) or 18 minutes (for INP clones). Larvae were collected and plated at low density on standard medium. MARCM clones were then recovered at the wandering third larval instar or at the adult stage.
To determine when DM lineage-specific apoptosis occurs during larval development, embryos of w; UAS-mCD8::GFP LL5 ; erm-Gal4 R09D11 were collected on agar plates for 4 hours and raised at 25°C for 22 hours. Larvae were collected, and then raised on standard medium at 25°C for 48, 60, 72, 84, and 96 hours before their brains were dissected. To study apoptosis in pupal brains, white pupae of w; UAS-mCD8::GFP LL5 ; erm-Gal4 R09D11 were collected and raised at 25°C for 6, 12, 24, 32, 48, and 72 hours before brain dissection. Apoptotic cells were detected in these brains by immunostaining with anti-activated Caspase-3 antibodies.
Immunohistochemistry and antibodies
Larval brains were dissected in ice-cold PBS and fixed in 2% paraformaldehyde (PFA) for 60 minutes at room temperature, washed several times in PBS/0.5% Triton X-100, and pre-incubated in 10% normal goat serum. Brains were incubated with primary antibodies overnight at 4°C, and with secondary antibodies for 2 to 3 hours at room temperature. Pupal brains were dissected in ice-cold PBS and fixed in 4% PFA for 30 minutes at room temperature, and washed several times in PBS/0.5% Triton X-100. Brains were incubated with primary and secondary antibodies, each for 24 hours at 4°C. Adult brains were dissected from 4 to 7-day-old females in ice-cold PBS and fixed in 4% PFA for 30 minutes at room temperature, and washed several times in PBS/0.5% Triton X-100. Brains were incubated with primary antibodies for 48 hours at 4°C, and with secondary antibodies for 48 hours at 4°C.
Primary antibodies used in this study were: chicken anti-green fluorescent protein (GFP) (1:1000; ab13970; Abcam, Cambridge, MA, USA); mouse anti-Repo (1:30; 8D12; Developmental Studies Hybridoma Bank (DSHB), Iowa City, IA, USA); mouse anti-neurotactin (1:20; BP106; DSHB); rat anti-Elav (1:30; DSHB); rabbit anti-activated Caspase-3 (Asp175) (1:100; Cell Signaling Technology, Beverly, MA, USA); mouse anti-nc82 (1:50; a gift from J. Pielage). Secondary antibodies were: Alexa 488-, Alexa 568-, and Alexa 647-conjugated anti-chicken, -rabbit, -rat, or -mouse IgG (all 1:500; all from Molecular Probes Inc., Eugene, OR, USA).
Microscopy and image processing
Immunofluorescent images were recorded on a confocal microscope (TCS SP5; Leica, Heerbrugg, Switzerland), and processed using ImageJ and Photoshop (Adobe Systems Inc., San Jose, CA, USA) software. Cells representing DM1/2 lineages in wild-type and H99 MARCM clones were counted using the Cell Counter plugin for ImageJ (K. De Vos).
List of abbreviations
after larval hatching
after puparium formation
Developmental Studies Hybridoma Bank
green fluorescent protein
ganglion mother cell
intermediate neural progenitor
mosaic analysis with a repressible cell marker
secondary axon tract.
We thank Jan Pielage for nc82 antibodies; the Developmental Studies Hybridoma Bank and the Bloomington Drosophila Stock Center for antibodies and fly stocks, Bruno Bello, Gudrun Victorin, and other members of the Reichert lab for discussions and assistance, and Susanne Flister for excellent technical help. This work was supported by SNSF-NFP63 'Stem cells and regenerative medicine' grant 406340128006/1 and SNSF grant 31003A12488/1 to HR.
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