Morphogenesis of honeybee hypopharyngeal gland during pupal development
© The Author(s). 2017
Received: 6 January 2017
Accepted: 5 April 2017
Published: 20 April 2017
The hypopharyngeal gland of worker bees contributes to the production of the royal jelly fed to queens and larvae. The gland consists of thousands of two-cell units that are composed of a secretory cell and a duct cell and that are arranged in sets of about 12 around a long collecting duct.
By fluorescent staining, we have examined the morphogenesis of the hypopharyngeal gland during pupal life, from a saccule lined by a pseudostratified epithelium to the elaborate organ of adult worker bees. The hypopharyngeal gland develops as follows. (1) Cell proliferation occurs during the first day of pupal life in the hypopharyngeal gland primordium. (2) Subsequently, the epithelium becomes organized into rosette-like units of three cells. Two of these will become the secretory cell and the duct cell of the adult secretory units; the third cell contributes only temporarily to the development of the secretory units and is eliminated by apoptosis in the second half of pupal life. (3) The three-cell units of flask-shaped cells undergo complex changes in cell morphology. Thus, by mid-pupal stage, the gland is structurally similar to the adult hypopharyngeal gland. (4) Concomitantly, the prospective secretory cell attains its characteristic subcellular organization by the invagination of a small patch of apical membrane domain, its extension to a tube of about 100 μm in length (termed a canaliculus), and the expansion of the tube to a diameter of about 3 μm. (6) Finally, the canaliculus-associated F-actin system becomes reorganized into rings of bundled actin filaments that are positioned at regular distances along the membrane tube.
The morphogenesis of the secretory units in the hypopharyngeal gland of the worker bee seems to be based on a developmental program that is conserved, with slight modification, among insects for the production of dermal glands. Elaboration of the secretory cell as a unicellular seamless epithelial tube occurs by invagination of the apical membrane, its extension likely by targeted exocytosis and its expansion, and finally the reorganisation of the membrane-associated F-actin system. Our work is fundamental for future studies of environmental effects on hypopharyngeal gland morphology and development.
KeywordsExocrine gland Insect Epithelial tube Organogenesis Cell polarity Actin cytoskeleton Apoptosis Invagination
The European honey bee (Apis mellifera) forms highly organized colonies that function as a superorganism . The majority of individuals in a bee colony, the sterile worker bees, support the queen, the drones, and the brood by undertaking various tasks in a temporal sequence . During the first 2 weeks after their emergence, worker bees perform activities within the hive, i.e., cleaning cells, caring for the brood and the queen, ripening nectar, and constructing combs. As the worker bees age to 2-3 weeks, they assume extra-nidal tasks, in particular foraging for pollen, nectar, and water. These behavioral alterations accompany changes in transcriptional and translational activity, physiology, and morphology [9, 11, 18, 23, 30, 44, 46, 48, 49]. In particular, the hypopharyngeal gland in worker bees has a developmental cycle closely related to the division of labor. The paired hypopharyngeal gland is an exocrine gland specific to hymenopterans, is located in the front of the head capsule, and delivers its proteinaceous secretory product via a large collecting duct to the hypopharynx . In nursing bees, this gland is voluminous, has a high secretory activity, and contributes to the production of royal jelly, which is fed to future queens and, to a lesser extent, to worker larvae . As the worker bees start foraging, their hypopharyngeal glands decrease in size, secrete at a lower rate, and produce a different protein blend including enzymes involved in carbohydrate metabolism [9, 30, 44].
From a cell-biological perspective, the canaliculus of the secretory cells is peculiar. This structure has been suggested to represent the apical domain of the plasma membrane involuted into the cell . Only recently, however, has molecular evidence been provided in support of this notion. Richter et al.  have demonstrated that phosphorylated (=activated) moesin, an apical membrane marker that links actin filaments to integral membrane proteins, is associated with and confined to the canalicular membrane. The cytoskeletal system affiliated to the canaliculus is also special. Rings of actin filaments encircle the membrane tubule at regular distances, whereas a sparse web of actin filaments is associated with the inter-ring portions of the canaliculus [21, 22, 35]. These actin rings are thought to provide a stabilizing framework to the canalicular membrane system during phases of high exocytic activity .
The anatomy and the cellular and subcellular organization of the hypopharyngeal glands in the adult worker bee have been studied extensively by use of various techniques, i.e., histology, electron microscopy, and fluorescence microscopy (e.g., [9, 16, 21–23, 31, 35]). In particular, several studies have addressed the structural changes that occur in hypopharyngeal gland as worker bees age and/or adopt other tasks [9, 23, 31, 35]. Of special interest is also the influence of pesticides on the morphology and physiology of adult hypopharyngeal glands and, thus, of the adverse side effects of these substances on honeybee vigor [16, 45]. In contrast, the organogenesis of the hypopharyngeal glands and the morphogenesis of the various gland cells have not been characterized as yet in detail. By use of histological techniques, Painter  has examined pupal gland cells, without noting the exact developmental stage, and has provided evidence for the transient presence of an additional cell type besides the secretory cell and duct cell during the morphogenesis of the gland units. Subsequently, da Cruz-Landim and Mello  have analyzed hypopharyngeal gland morphogenesis during pupal life by using histological techniques, but in the stingless bee Melipona quadrifasciata anthidioides. Since none of these studies has examined the morphogenesis of secretory cells at the subcellular level, the time and the manner in which the secretory cells form their distinctive apical membrane system, the canaliculus, remain mysterious. This topic is of genuine interest in view of the recent finding that insecticides impair brood development .
In the present study, we have attempted to track the origin of the secretory and duct cells during pupal hypopharyngeal gland development by using the DNA-binding dye DAPI and the F-actin-binding phalloidin to visualize nuclei and the cell outline, respectively. We confirm the transient existence of an additional cell type between the secretory cell and duct cell, and that this cell is lost at the mid-pupal stage by apoptosis. Moreover, we examine the development of the canalicular system and the establishment of the associated rings of actin filaments in secretory cells.
Gross morphology of hypopharyngeal glands during pupal development
Pupae were staged from P1 to P9, equivalent to days of pupal development [12, 14]. At developmental stage P1, two saccule-like evaginations, representing hypopharyngeal gland primordia, extended from the ventral side of the pharynx (Fig. 2a and c). The saccules consisted of a transparent epithelium enclosing a large lumen, had a smooth outer surface, and measured about 0.5 mm in length and 0.2 mm in width. During subsequent days of pupal developmental up to stage P4, the hypopharyngeal gland primordia increased in length to about 5 mm, their width declined to about 0.1 mm, and their outer surface became undulating (Fig. 2d and e). By stage P5, a collecting duct of approximately 40 μm in width extended on the medial axis along the entire hypopharyngeal glands. Numerous cauliflower-like structures, representing future acini, were arranged around the duct, being linked to it by stalks that were approximately 20 μm long and 20 μm thick (Fig. 2f). Because of the large number of acini and their proximity to the duct and to each other, the collecting duct was almost completely masked from sight. By stage P6, the hypopharyngeal glands had adopted a gross morphology similar to that of adult glands (Fig. 2g-i), with numerous acini of ovoid shape linked via bundles of ductules of approximately 50 μm in length to the collecting duct that extended over the entire length of the gland.
Additional file 1: Animation of an image stack through a hypopharyngeal gland primordium, stained with phalloidin (green) and DAPI (blue). Whole-mount specimen; inter-plane distance, 0.34 μm; objective lens, Zeiss C-Apochromat 40x/1.2 W. See Fig. 3a-f for details. (AVI 10486 kb)
Cellular morphology of developing hypopharyngeal glands
Additional file 2: Animation of an image stack through a hypopharyngeal gland at pupal stage P2/3, stained with phalloidin (green) and DAPI (blue). Cryosection; inter-plane distance, 0.37 μm; objective lens, Zeiss Plan-Apochromat 63x/1.4 Oil. See Fig. 5a-c for details. (AVI 514 kb)
At developmental stage P4, acini primorida bulged in a basal direction from the epithelial layer (Fig. 4c). Ductule precursors had increased in length to about 20 μm and were composed of a prospective duct cell almost over their entire length, except for a short segment lying next to the secretory cell and produced by an accessory cell (Fig. 5e-h; Additional file 3). The secretory cell process was shortened, retracted in a basal direction, and contained an onion-shaped F-actin-rich structure next to the distal end of the ductule. We consider that this structure corresponds to an array of microvilli and represents the origin for the development of the secretory cell canaliculus (see below).
Additional file 3: Animation of an image stack through a hypopharyngeal gland at pupal stage P4, stained with phalloidin (green) and DAPI (blue). Cryosection; inter-plane distance, 0.24 μm; objective lens, Zeiss Plan-Apochromat 63x/1.4 Oil. See Fig. 5e-g for details. (AVI 2590 kb)
Differentiation of the canaliculus
Since the timing and manner of formation of the canaliculus of the secretory cells are unknown, we wished to analyze this morphogenetic process by the use of probes specific for this membrane domain. We have shown previously that anti-phosphorylated ERM (anti-pERM) and anti-phosphotyrosine selectively stain the canalicular system of adult secretory cells. Whereas anti-pERM outlines membrane segments between adjacent actin rings, anti-phosphotyrosine identifies dot-like structures that are associated with the canaliculus and that may represent microvillar tips . Unfortunately, however, neither anti-pERM nor anti-phosphotyrosine stained any structures in prospective secretory cells of the pupal hypopharyngeal glands, suggesting that either these cells lack a canaliculus throughout pupal development, or that the expression of these proteins and/or their localization to the canalicular membrane occurs after the formation of the canalicular membrane system. Thus, we could only rely on the subcellular distribution of F-actin to probe the formation of the canalicular membrane, assuming that the F-actin assemblies in the interior of the secretory cells are associated with this membrane domain and/or its precursors.
Additional file 5: Animation of an image stack through a hypopharyngeal gland at pupal stage P5, stained with phalloidin (green) and DAPI (blue). Whole-mount specimen; inter-plane distance, 0.29 μm; objective lens, Zeiss C-Apochromat 40x/1.2 W. See Fig. 7a for details. (AVI 670 kb)
Animation of an image stack through a hypopharyngeal gland at pupal stage P5, stained with phalloidin (green) and DAPI (blue). Whole-mount specimen; inter-plane distance, 0.29 μm; objective lens, Zeiss C-Apochromat 40x/1.2 W. See Fig. 4d for details. (AVI 8006 kb)
Animation of an image stack through a hypopharyngeal gland at pupal stage P5, stained with phalloidin (green) and DAPI (blue). Whole-mount specimen; inter-plane distance, 0.29 μm; objective lens, Zeiss C-Apochromat 40x/1.2 W. This movie shows an area of the acinus presented in movie 6. See Fig. 7b-f for details. (AVI 411 kb)
At stage P6, the canaliculus was radially expanded to a diameter of 2.8 to 3.5 μm over its entire length, without any periodic constrictions. Canaliculus-associated F-actin was organized in a planar irregular web (Fig. 8c and i). Other than the canaliculus, no other F-actin assemblies were detected in the interior of the prospective secretory cells from this developmental stage on. By developmental stage P7/P8, canaliculus-associated F-actin was concentrated in closely spaced, frequently interconnected or fused rings, with a ring diameter of 2.5 to 3.0 μm (Fig. 8d and j). Areas between these F-actin assemblies were covered by a sparse matrix of actin filaments. During subsequent pupal development, the actin rings became more pronounced, the extent of the interconnections decreased, and the distance between the adjacent actin rings increased (Fig. 8e and k). In addition, the amount of F-actin associated with inter-ring portions seemed to decrease during the last few days of pupal development. Hence, canaliculi-associated actin rings were prominent and were regularly spaced with a few residual interconnections by the eclosion of the worker bees (Fig. 8f and l), as described previously .
Hypopharyngeal glands, being specific to hymenopterans, are quite diverse in morphological aspects . Whereas the two-cell unit of secretory cell and canal cell seems to be common, the modes in which these units are organized to hypopharyngeal glands vary between species. In particular, the units may be attached directly to the hypopharyngeal plate or deliver their secretory product via a more or less elaborate collecting duct to the hypopharynx. Moreover, two-cell units may be individually attached to the collecting duct, like in the stingless bee Melipona quadrifasciata anthidioides, or several two-cell units may be assembled to acini with bundled ductules, as in Apis mellifera. Unfortunately, hypopharyngeal gland development has been examined as yet only in M. quadrifasciata anthidioides, but by histological techniques . Nevertheless, since all hypopharyngeal glands are built of two-cell units, it may be supposed that the developmental program leading to these units is also shared among hymenopterans.
Development of secretory units
Dermal glands of insects exhibit an enormous diversity. On morphological criteria, they have been classified into three types, with class III being organized in basic units of secretory and support cells [28, 29]. The development of class III glands has been proposed to be based on a common mechanism. Each glandular unit is an isogenic group of four cells that are derived from one progenitor cell by sequential mitoses . Initially, these cells are concentrically wrapped one around another with, first, the innermost cell termed either the ciliary or basal cell, then the future secretory cell, and finally, the two outermost duct-forming cells [34, 38]. Subsequent apoptosis leads to mature gland units composed of fewer than four cells; at minimum, just one cell remains as a secretory cell.
In the present study, we visualized mitotic cells in the hypopharyngeal gland primordium, but we did not track the developmental fate of daughter cells. Nevertheless, our data are congruent with the above model of class-III-gland development in insects. Since secretory units in the hypopharyngeal gland of adult worker bees are composed merely of two cells, namely a secretory cell and a duct cell, two cells seem to be lacking in the case of the four-cell isogenic group. One of the cells missing in the adult state is the accessory cell that resides between the future duct and secretory cells during the first half of pupal life. The wrapping of these three cells around each other, with the future duct cell being the outermost and the prospective secretory cell lying on the inside, is reminiscent of the situation in the developing mandibular glands of the death’s head cockroach Blaberus craniifer and tergal glands of the male German cockroach Blattella germanica [34, 38]. The presence of an accessory cell in pupal hypopharyngeal glands has previously been described . Painter suggested that this cell, being transiently present, becomes “absorbed” by the secretory cell. Our data indicate, instead, an apoptotic fate for this cell after the formation and elaboration of the gland units. The other cell missing in the secretory units of the hypopharyngeal gland is the basal/ciliary cell that is located basal of the secretory cell in other insect glands. Conceivably, this cell is not produced in honeybee hypopharyngeal glands because of a change in cell lineage during gland evolution, as demonstrated for Drosophila spermathecae . Alternatively, the basal cell may undergo apoptosis soon after its production and thus does not contribute to the further development of the gland units. In support of the second option are the numerous apoptotic nuclei in the basal region of the P1 epithelium, concurrently with mitotic events.
In summary, we suggest the following model of cell lineage for the secretory units in the worker bee hypopharyngeal gland (Fig. 9b): mitosis of a progenitor cell produces four cells; one of them, localized basally, undergoes apoptosis shortly after genesis, whereas another one, the accessory cell, contributes to secretory unit morphogenesis but suffers cell death during late pupal development. The remaining two cells form the gland units (see below).
Development of the canaliculus
The two-cell secretory units of adult hypopharyngeal glands can be considered as epithelial tubes, with the tube lumen being circumscribed by the apical surface of the cells . The canal cell forms a continuous conduit that opens into the collecting duct, whereas the adjoining secretory cell contains the blind ending of the tube. Electron-microscopic imaging has demonstrated that both cells are linked by an intercellular junctional complex, but that the cells do not form autocellular junctions [2, 5, 35]. These fine-structural details enable the secretory units of the hypopharyngeal gland to be classified as unicellular seamless tubes.
The morphogenesis of seamless epithelial tubes has been analyzed in three different model systems, i.e., the vertebrate vascular system, the tracheal system of Drosophila, and the excretory system of Caenorhabditis elegans. These studies have demonstrated three ways in which unicellular epithelial tubes can be created [36, 37, 41]. First, vesicular structures in the cytoplasm of the cell merge and form a lumen that extends over the entire length of the cell and fuses finally at its two ends with the plasma membrane. This mechanism, termed cell hollowing, is involved in the formation of vertebrate blood vessels and of the excretory canal cell in C. elegans [6, 19]. Second, a patch of apical membrane circumscribed by intercellular junctions enlarges by exocytosis and extends internally into the cell. Such apical invagination in combination with apically directed exocytosis has been detected in the case of the development of the tracheal terminal cells of Drosophila  and of the blood vessels of the zebrafish . Finally, as in the case of the excretory duct cell of C. elegans, an epithelial cell wraps itself up with its apical surface towards the inside, forms an autocellular junction to close the tube, and subsequently removes the junction .
At P2/P3, the earliest time-point at which a tubular structure could be identified in the hypopharyngeal gland primordium, the short ductule was connected to the apical surface of the epithelium, was continuous, and was apparently formed by three cells arranged in a row, with the future duct cell and the accessory cell molding the tube and with the prospective secretory cell closing off the distal end of the tube. Unfortunately, we were unable to visualize the initial step of tube formation. However, since all cells in the pseudostratified epithelium reach to the luminal surface and hold an apical domain, cell wrapping or invagination may account for the creation of the ductule precursor. Discrimination between these possibilities requires the imaging of the junctional complexes. Since antibodies against Drosophila junctional proteins did not cross-react with their honeybee homologues , we are currently unable to characterize the initial process of ductule formation.
In the case of secretory cells and their canaliculus, our data are in agreement with an invagination and apically targeted exocytosis. At developmental interval P2 to P4, the prospective secretory cell contacts the distal end of the ductule with a small surface area that is enriched with F-actin. We suggest that the F-actin at this site reflects the presence of microvilli, as demonstrated in glands by electron microscopy of developing secretory cells in the female accessory of Rhodnius prolixus . During the P5 stage, a continuous tube grows from this site inwards into the future secretory cell to reach a final length of about 100 μm. Spheroidal F-actin structures in the vicinity of the developing tube are indicative of membrane material for tube extension.
In various insect dermal glands, yet another, completely different mechanism has been reported for the formation of the canaliculus of secretory cells [3, 34, 38]. A basal cell, located basally to the future secretory cell, extends a ciliary process that pierces the future secretory and duct cells to form a mold for the canaliculus and the duct. Subsequently, the ciliary process retracts and the basal cell degenerates. Although we did not attempt to localize cilia, such a mechanism can be rejected in the case of hypopharyngeal gland morphogenesis since basal cells are absent, at least during the period of canaliculus formation. Similarly, ductule morphogenesis in the female accessory glands in Rhodnius prolixus and in Drosophila spermathecae has been reported to occur without the contribution of a ciliary process [24, 40].
After the generation of the canaliculus in full length in the secretory cell, the tube becomes elaborated. Accordion-like folding of the tube wall at this developmental stage indicates an increase in surface area, apparently as a stockpile for later expansion. The presence of F-actin-bounded vesicular structures in the cytoplasm alongside the canaliculus during this developmental stage indicates that the surface increase is fed by the lateral fusion of vesicles. Likewise, new membrane material is added by way of vesicles along the tube of the apical membrane in the terminal tracheal cells of Drosophila . Subsequently, the canaliculus expands to a uniform diameter of about 3 μm. This process may be driven by ion and water transport into the canaliculus, like the aquaporin-dependent increase in lumen size in the excretory canal cell of C. elegans . Alternatively or concomitantly, the canaliculus might become inflated and stabilized by the deposition of chitin in the lumen [10, 37, 43].
Differentiation of the F-actin system associated with the canalicular membrane
A network of F-actin is generally associated with the luminal membrane of epithelial tubes [13, 37]. This feature enabled the imaging of the developing canaliculus in the hypopharyngeal gland secretory cells, despite antibodies against marker proteins for the apical membrane not working in the present study. We have demonstrated that the F-actin system that is attached to the canalicular membrane is reorganized during the second half of pupal life. At developmental stage P6, when the canalicular system is formed to its full extent, a web of actin filaments with a seemingly random orientation surrounds the canalicular tube. F-actin then becomes gradually concentrated in rings, with the amount of interconnections decreasing and the inter-ring distance increasing. This change in actin cytoskeletal organization probably is concomitant or is attributable to a switch in the actin-binding proteins (ABPs) associated with the actin filaments on the canalicular membrane. Whereas cross-linking ABPs such as spectrin produce orthogonal arrays of actin filaments, bundling ABPs such as the Kelch protein of Drosophila can produce tight bundles of parallel actin filaments . In agreement with this hypothesis is the finding that spectrin is not detectable with canaliculus-associated F-actin in adult secretory cells . Moreover, the formation of actin rings in the ovarian ring canals of Drosophila depends on Kelch . The expression of hDKIR, a human homologue of the Drosophila Kelch protein, produces ring-like actin structures in cultured mammalian cells .
Actin rings seem to be characteristic of secretory cells in hymenopteran hypopharyngeal glands. However, species-specific differences occur with respect to the diameter, the level of interconnections, and the distance between the actin rings [1, 22]. In particular, in the stingless bee Tetragonula carbonaria, actin rings on the canaliculus have frequent connections and are often not closed , thus resembling the P7/P8 intermediate stage in worker bees. We suggest that the differences in the relative expression of cross-linking and bundling ABPs account for these differences in actin ring organization between species.
We have described the various steps of hypopharyngeal gland development from the pupal primordium to the intricate organ that adult worker bees possess at emergence. The gland develops as follows: cell proliferation in a pseudostratified epithelium, formation and morphogenesis of three-cell units within the epithelial layer, removal of accessory cells from the three cell units to obtain the final units of a duct cell and a secretory cell, elaboration of the canaliculus in the latter cell by invagination, extension and expansion of apical membrane, and finally reorganization of the canaliculus-associated actin cytoskeleton to form distinctive actin rings. Based on these findings, the effects of environmental factors, such as insecticides, on gland development can be explored. Moreover, since species-specific differences in the organization of the canaliculus-associated F-actin system have been reported, an analysis of hypopharyngeal gland development in other hymenopteran species might be informative.
Animals and preparation
Pupae of worker bees (Apis mellifera) were taken from combs with sealed broods and were kept in a humidified incubator at 34 °C. Pupae were staged from P1 to P9 by using morphological criteria, i.e., pigmentation of the eyes, bodies, and legs [12, 14]. Pupal stages P2 and P3 and stages P7 and P8 could not be discriminated unambiguously; hence, we pooled these stages into P2/P3 and P7/P8, respectively. Newly emerged worker bees (stage A0) were collected off the comb just after emergence. Animals were decapitated, the head capsule was opened on the frontal side with a microscalpel, and the hypopharyngeal glands were removed in Ringer solution (270 mM NaCl, 3.2 mM KCl, 1.2 mM CaCl2, 10 mM MgCl2, 10 mM morpholinopropansulfonic acid, pH 7.3) and immediately transferred to fixative (3% paraformaldehyde, 1 mM dithiobis(succinimidyl proprionate), 0.1 M phosphate buffer, pH 7.0).
The following antibodies were used: monoclonal rabbit antibody against phosphorylated ezrin/radixin/moesin (pERM; product # 3149; Cell Signaling, Danvers, MA, USA), monoclonal mouse antibody clone PY99 against phosphotyrosine (pY; Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA), and polyclonal rabbit antibody against histone H3 phosphorylated at Ser10 (H3-P; product # 06–570; Merck Millipore, Billerica, MA, USA). Cross-reactivity of anti-pERM with honeybee moesin has been demonstrated previously .
Fluorescence staining and imaging
After fixation for 1 h at room temperature, specimens were washed, cryofixed in melting isopentane (ca. -150 °C), cryosectioned at a thickness of about 10 μm, and stained with antibodies, 4′,6-diamidino-2-phenylindole (DAPI), and AlexaFluor 488 phalloidin (Life Technologies GmbH; Darmstadt, Germany) or CF488A phalloidin (Biotium Inc., Hayward, CA, USA) as described in detail previously . To label entire glands, fixed glands were (1) washed 3 × 10 min in phosphate-buffered saline (PBS), (2) permeabilized with 0.01% Tween20 in PBS for 10 min, (3) treated with 50 mM NH4Cl in PBS for 10 min, and (4) washed 1 × 10 min in PBS. After (5) treatment with blocking solution (1% normal goat serum, 0.8% bovine serum albumine, 0.5% Triton X-100 in PBS) for 15 min, specimens were (6) incubated over-night at 4 °C with anti-H3-P diluted in blocking solution, (7) washed 3 × 15 min in PBS, (8) incubated for 3 h at room temperature with Cy3-conjugated goat anti-rabbit IgG, fluorophore-tagged phalloidin, and DAPI in PBS, (9) washed again 3 × 15 min in PBS, and (10) embedded in Mowiol 4–88 mounting medium supplemented with 2% propyl gallate as an antifade reagent. In the case of the labeling of entire glands with phalloidin and DAPI only, steps 2–7 were omitted, and the specimens were incubated for 3 h or over-night with fluorophore-tagged phalloidin and DAPI, diluted in blocking solution. Fluorescence images were recorded with LSM 510, LSM 710, or LSM 880-Airyscan confocal microscopes and processed (3D presentation, gamma correction as noted in figure legends) with ZEN software (Carl Zeiss Microscopy GmbH, Jena, Germany).
Histone H3 phosphorylated at Ser10
We are grateful to Ricarda Scheiner and to Markus Thamm for providing honeybees, to Carl Zeiss Microscopy GmbH for providing access to a LSM880-Airyscan, to Bärbel Wuntke for technical assistance, and to Dr. Theresa Jones for language editing. We acknowledge the support of the Deutsche Forschungsgemeinschaft and Open Access Publishing Fund of University of Potsdam.
Availability of data and materials
The data supporting the results of this manuscript are included in the body of the manuscript and in the additional files.
SPK, DR, and OB conceived and designed the experiments; SPK and DR performed animal dissection and immunochemistry; SPK and OB collected and analyzed the data; OB wrote the paper. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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